Cdc42 is a conserved Rho-family small GTPase that functions as a GDP/GTP-regulated molecular switch. Active GTP-bound Cdc42 binds effectors such as WASP/N-WASP, PAK, and Par6/aPKC polarity complexes to organize cortical actin, filopodia, cell polarity, junctions, migration, endocytosis, cytokinesis, and spindle-related processes. Its outputs depend strongly on membrane targeting and isoform-specific C-terminal lipidation: the broadly expressed prenylated isoform acts at leading-edge/cortical membranes, while a brain-enriched palmitoylated isoform contributes to intracellular membrane and neuronal contexts.
| GO Term | Evidence | Action | Reason |
|---|---|---|---|
|
GO:0003924
GTPase activity
|
IBA
GO_REF:0000033 |
ACCEPT |
Summary: GTPase activity is consistent with core Cdc42 GTPase, cytoskeletal, polarity, or localization biology.
Reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane localization, or immediate actin/polarity outputs.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
CDC42 is a **GTP-hydrolyzing enzyme** (small GTPase). Its substrate is **GTP**, which it binds and hydrolyzes to **GDP + Pi**
|
|
GO:0005525
GTP binding
|
IBA
GO_REF:0000033 |
ACCEPT |
Summary: GTP binding is consistent with core Cdc42 GTPase, cytoskeletal, polarity, or localization biology.
Reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane localization, or immediate actin/polarity outputs.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
CDC42 is a **GTP-hydrolyzing enzyme** (small GTPase). Its substrate is **GTP**, which it binds and hydrolyzes to **GDP + Pi**
|
|
GO:0007165
signal transduction
|
IBA
GO_REF:0000033 |
MODIFY |
Summary: signal transduction is a broad ancestor for the Cdc42 signaling role.
Reason: Cdc42 is best represented as a small GTPase/Rho-family signaling switch.
Proposed replacements:
small GTPase-mediated signal transduction
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
CDC42 belongs to the **Rho family** of small GTPases and acts as a **molecular switch** cycling between **GTP-bound (active)** and **GDP-bound (inactive)** states
|
|
GO:0005886
plasma membrane
|
IBA
GO_REF:0000033 |
ACCEPT |
Summary: plasma membrane is consistent with core Cdc42 GTPase, cytoskeletal, polarity, or localization biology.
Reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane localization, or immediate actin/polarity outputs.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
CDC42 associates with the **plasma membrane/cell cortex** via a **carboxy-terminal prenyl group**
|
|
GO:0007015
actin filament organization
|
IBA
GO_REF:0000033 |
ACCEPT |
Summary: actin filament organization is consistent with core Cdc42 GTPase, cytoskeletal, polarity, or localization biology.
Reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane localization, or immediate actin/polarity outputs.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
CDC42 is directly linked to actin nucleation pathways through **WASP-family nucleation-promoting factors**.
|
|
GO:0030010
establishment of cell polarity
|
IBA
GO_REF:0000033 |
ACCEPT |
Summary: establishment of cell polarity is consistent with core Cdc42 GTPase, cytoskeletal, polarity, or localization biology.
Reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane localization, or immediate actin/polarity outputs.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
CDC42b supports **N-WASP-mediated endocytosis** from intracellular compartments.
|
|
GO:0006897
endocytosis
|
IBA
GO_REF:0000033 |
KEEP AS NON CORE |
Summary: endocytosis is a supported Cdc42 cellular output, but it is not the core small GTPase catalytic function.
Reason: Cdc42 GTP-bound effector signaling can influence trafficking and membrane dynamics, but this process should be treated as context-specific.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
In its **GTP-bound state**, CDC42 binds effector proteins that drive downstream cytoskeletal and polarity responses
|
|
GO:0019901
protein kinase binding
|
IBA
GO_REF:0000033 |
ACCEPT |
Summary: protein kinase binding is consistent with core Cdc42 GTPase, cytoskeletal, polarity, or localization biology.
Reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane localization, or immediate actin/polarity outputs.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
CDC42 is directly linked to actin nucleation pathways through **WASP-family nucleation-promoting factors**.
|
|
GO:0051489
regulation of filopodium assembly
|
IBA
GO_REF:0000033 |
ACCEPT |
Summary: regulation of filopodium assembly is consistent with core Cdc42 GTPase, cytoskeletal, polarity, or localization biology.
Reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane localization, or immediate actin/polarity outputs.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
CDC42 is directly linked to actin nucleation pathways through **WASP-family nucleation-promoting factors**.
|
|
GO:0000166
nucleotide binding
|
IEA
GO_REF:0000043 |
MODIFY |
Summary: Nucleotide binding is too broad for Cdc42.
Reason: Cdc42 specifically binds guanine nucleotides and functions through GTP/GDP cycling.
Proposed replacements:
GTP binding
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
CDC42 is a **GTP-hydrolyzing enzyme** (small GTPase). Its substrate is **GTP**, which it binds and hydrolyzes to **GDP + Pi**
|
|
GO:0003924
GTPase activity
|
IEA
GO_REF:0000120 |
ACCEPT |
Summary: GTPase activity is consistent with core Cdc42 GTPase, cytoskeletal, polarity, or localization biology.
Reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane localization, or immediate actin/polarity outputs.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
CDC42 is a **GTP-hydrolyzing enzyme** (small GTPase). Its substrate is **GTP**, which it binds and hydrolyzes to **GDP + Pi**
|
|
GO:0003925
G protein activity
|
IEA
GO_REF:0000003 |
ACCEPT |
Summary: G protein activity is consistent with core Cdc42 GTPase, cytoskeletal, polarity, or localization biology.
Reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane localization, or immediate actin/polarity outputs.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
CDC42 is a **GTP-hydrolyzing enzyme** (small GTPase). Its substrate is **GTP**, which it binds and hydrolyzes to **GDP + Pi**
|
|
GO:0005525
GTP binding
|
IEA
GO_REF:0000120 |
ACCEPT |
Summary: GTP binding is consistent with core Cdc42 GTPase, cytoskeletal, polarity, or localization biology.
Reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane localization, or immediate actin/polarity outputs.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
CDC42 is a **GTP-hydrolyzing enzyme** (small GTPase). Its substrate is **GTP**, which it binds and hydrolyzes to **GDP + Pi**
|
|
GO:0005737
cytoplasm
|
IEA
GO_REF:0000120 |
ACCEPT |
Summary: cytoplasm is consistent with core Cdc42 GTPase, cytoskeletal, polarity, or localization biology.
Reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane localization, or immediate actin/polarity outputs.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
CDC42 associates with the **plasma membrane/cell cortex** via a **carboxy-terminal prenyl group**
|
|
GO:0005813
centrosome
|
IEA
GO_REF:0000120 |
ACCEPT |
Summary: centrosome is consistent with core Cdc42 GTPase, cytoskeletal, polarity, or localization biology.
Reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane localization, or immediate actin/polarity outputs.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
CDC42 is directly linked to actin nucleation pathways through **WASP-family nucleation-promoting factors**.
|
|
GO:0005819
spindle
|
IEA
GO_REF:0000044 |
REMOVE |
Summary: This automated generic cellular-component transfer is too broad relative to the narrower Cdc42 localization annotations retained elsewhere.
Reason: The local evidence does not justify keeping this broad automated component row as a separate accepted annotation; it was previously supported only by unrelated actin-effector biology.
|
|
GO:0005886
plasma membrane
|
IEA
GO_REF:0000120 |
ACCEPT |
Summary: plasma membrane is consistent with core Cdc42 GTPase, cytoskeletal, polarity, or localization biology.
Reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane localization, or immediate actin/polarity outputs.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
CDC42 associates with the **plasma membrane/cell cortex** via a **carboxy-terminal prenyl group**
|
|
GO:0007264
small GTPase-mediated signal transduction
|
IEA
GO_REF:0000002 |
ACCEPT |
Summary: small GTPase-mediated signal transduction is consistent with core Cdc42 GTPase, cytoskeletal, polarity, or localization biology.
Reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane localization, or immediate actin/polarity outputs.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
CDC42 is directly linked to actin nucleation pathways through **WASP-family nucleation-promoting factors**.
|
|
GO:0007399
nervous system development
|
IEA
GO_REF:0000043 |
KEEP AS NON CORE |
Summary: nervous system development is a supported context-specific Cdc42 output.
Reason: Cdc42 controls broad cellular architecture and developmental programs through actin, polarity, trafficking, and kinase-effector pathways, but this term is not the core molecular function.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
In its **GTP-bound state**, CDC42 binds effector proteins that drive downstream cytoskeletal and polarity responses
|
|
GO:0009653
anatomical structure morphogenesis
|
IEA
GO_REF:0000117 |
KEEP AS NON CORE |
Summary: anatomical structure morphogenesis is a supported context-specific Cdc42 output.
Reason: Cdc42 controls broad cellular architecture and developmental programs through actin, polarity, trafficking, and kinase-effector pathways, but this term is not the core molecular function.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
In its **GTP-bound state**, CDC42 binds effector proteins that drive downstream cytoskeletal and polarity responses
|
|
GO:0016787
hydrolase activity
|
IEA
GO_REF:0000043 |
MODIFY |
Summary: Hydrolase activity is too broad for Cdc42.
Reason: The relevant hydrolytic activity is GTPase activity in a Rho-family molecular switch.
Proposed replacements:
GTPase activity
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
CDC42 is a **GTP-hydrolyzing enzyme** (small GTPase). Its substrate is **GTP**, which it binds and hydrolyzes to **GDP + Pi**
|
|
GO:0030154
cell differentiation
|
IEA
GO_REF:0000043 |
KEEP AS NON CORE |
Summary: cell differentiation is a supported context-specific Cdc42 output.
Reason: Cdc42 controls broad cellular architecture and developmental programs through actin, polarity, trafficking, and kinase-effector pathways, but this term is not the core molecular function.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
In its **GTP-bound state**, CDC42 binds effector proteins that drive downstream cytoskeletal and polarity responses
|
|
GO:0030425
dendrite
|
IEA
GO_REF:0000044 |
KEEP AS NON CORE |
Summary: dendrite is a supported context-specific Cdc42 output.
Reason: Cdc42 controls broad cellular architecture and developmental programs through actin, polarity, trafficking, and kinase-effector pathways, but this term is not the core molecular function.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
In its **GTP-bound state**, CDC42 binds effector proteins that drive downstream cytoskeletal and polarity responses
|
|
GO:0030496
midbody
|
IEA
GO_REF:0000120 |
ACCEPT |
Summary: midbody is consistent with core Cdc42 GTPase, cytoskeletal, polarity, or localization biology.
Reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane localization, or immediate actin/polarity outputs.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
CDC42 is directly linked to actin nucleation pathways through **WASP-family nucleation-promoting factors**.
|
|
GO:0031258
lamellipodium membrane
|
IEA
GO_REF:0000044 |
ACCEPT |
Summary: lamellipodium membrane is consistent with core Cdc42 GTPase, cytoskeletal, polarity, or localization biology.
Reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane localization, or immediate actin/polarity outputs.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
CDC42 is directly linked to actin nucleation pathways through **WASP-family nucleation-promoting factors**.
|
|
GO:0051130
positive regulation of cellular component organization
|
IEA
GO_REF:0000117 |
KEEP AS NON CORE |
Summary: positive regulation of cellular component organization is a supported context-specific Cdc42 output.
Reason: Cdc42 controls broad cellular architecture and developmental programs through actin, polarity, trafficking, and kinase-effector pathways, but this term is not the core molecular function.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
In its **GTP-bound state**, CDC42 binds effector proteins that drive downstream cytoskeletal and polarity responses
|
|
GO:0071944
cell periphery
|
IEA
GO_REF:0000117 |
ACCEPT |
Summary: cell periphery is consistent with core Cdc42 GTPase, cytoskeletal, polarity, or localization biology.
Reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane localization, or immediate actin/polarity outputs.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
CDC42 associates with the **plasma membrane/cell cortex** via a **carboxy-terminal prenyl group**
|
|
GO:0005515
protein binding
|
IPI
PMID:12123608 Plexin-B1 directly interacts with PDZ-RhoGEF/LARG to regulat... |
MARK AS OVER ANNOTATED |
Summary: protein binding records a physical association but is too generic to describe the gene product function.
Reason: The evidence supports regulated signaling-complex assembly, not a meaningful standalone protein binding function; more informative molecular and pathway terms capture the biology.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
In its **GTP-bound state**, CDC42 binds effector proteins that drive downstream cytoskeletal and polarity responses
|
|
GO:0005515
protein binding
|
IPI
PMID:15537656 A direct interaction between Cdc42 and vesicle-associated me... |
MARK AS OVER ANNOTATED |
Summary: protein binding records a physical association but is too generic to describe the gene product function.
Reason: The evidence supports regulated signaling-complex assembly, not a meaningful standalone protein binding function; more informative molecular and pathway terms capture the biology.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
In its **GTP-bound state**, CDC42 binds effector proteins that drive downstream cytoskeletal and polarity responses
|
|
GO:0005515
protein binding
|
IPI
PMID:18325335 Affixin activates Rac1 via betaPIX in C2C12 myoblast. |
MARK AS OVER ANNOTATED |
Summary: protein binding records a physical association but is too generic to describe the gene product function.
Reason: The evidence supports regulated signaling-complex assembly, not a meaningful standalone protein binding function; more informative molecular and pathway terms capture the biology.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
In its **GTP-bound state**, CDC42 binds effector proteins that drive downstream cytoskeletal and polarity responses
|
|
GO:0005515
protein binding
|
IPI
PMID:18541910 Bves directly interacts with GEFT, and controls cell shape a... |
MARK AS OVER ANNOTATED |
Summary: protein binding records a physical association but is too generic to describe the gene product function.
Reason: The evidence supports regulated signaling-complex assembly, not a meaningful standalone protein binding function; more informative molecular and pathway terms capture the biology.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
In its **GTP-bound state**, CDC42 binds effector proteins that drive downstream cytoskeletal and polarity responses
|
|
GO:0005515
protein binding
|
IPI
PMID:18854161 ACF7 regulates cytoskeletal-focal adhesion dynamics and migr... |
MARK AS OVER ANNOTATED |
Summary: protein binding records a physical association but is too generic to describe the gene product function.
Reason: The evidence supports regulated signaling-complex assembly, not a meaningful standalone protein binding function; more informative molecular and pathway terms capture the biology.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
In its **GTP-bound state**, CDC42 binds effector proteins that drive downstream cytoskeletal and polarity responses
|
|
GO:0005515
protein binding
|
IPI
PMID:19893577 The adenomatous polyposis coli-associated exchange factors A... |
MARK AS OVER ANNOTATED |
Summary: protein binding records a physical association but is too generic to describe the gene product function.
Reason: The evidence supports regulated signaling-complex assembly, not a meaningful standalone protein binding function; more informative molecular and pathway terms capture the biology.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
In its **GTP-bound state**, CDC42 binds effector proteins that drive downstream cytoskeletal and polarity responses
|
|
GO:0005515
protein binding
|
IPI
PMID:23706742 RAS and RHO families of GTPases directly regulate distinct p... |
MARK AS OVER ANNOTATED |
Summary: protein binding records a physical association but is too generic to describe the gene product function.
Reason: The evidence supports regulated signaling-complex assembly, not a meaningful standalone protein binding function; more informative molecular and pathway terms capture the biology.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
In its **GTP-bound state**, CDC42 binds effector proteins that drive downstream cytoskeletal and polarity responses
|
|
GO:0006911
phagocytosis, engulfment
|
IEA
GO_REF:0000107 |
ACCEPT |
Summary: phagocytosis, engulfment is consistent with core Cdc42 GTPase, cytoskeletal, polarity, or localization biology.
Reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane localization, or immediate actin/polarity outputs.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
CDC42 is directly linked to actin nucleation pathways through **WASP-family nucleation-promoting factors**.
|
|
GO:0007015
actin filament organization
|
IEA
GO_REF:0000107 |
ACCEPT |
Summary: actin filament organization is consistent with core Cdc42 GTPase, cytoskeletal, polarity, or localization biology.
Reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane localization, or immediate actin/polarity outputs.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
CDC42 is directly linked to actin nucleation pathways through **WASP-family nucleation-promoting factors**.
|
|
GO:0007229
integrin-mediated signaling pathway
|
IEA
GO_REF:0000107 |
KEEP AS NON CORE |
Summary: integrin-mediated signaling pathway is a supported context-specific Cdc42 output.
Reason: Cdc42 controls broad cellular architecture and developmental programs through actin, polarity, trafficking, and kinase-effector pathways, but this term is not the core molecular function.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
In its **GTP-bound state**, CDC42 binds effector proteins that drive downstream cytoskeletal and polarity responses
|
|
GO:0010591
regulation of lamellipodium assembly
|
IEA
GO_REF:0000107 |
ACCEPT |
Summary: regulation of lamellipodium assembly is consistent with core Cdc42 GTPase, cytoskeletal, polarity, or localization biology.
Reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane localization, or immediate actin/polarity outputs.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
CDC42 is directly linked to actin nucleation pathways through **WASP-family nucleation-promoting factors**.
|
|
GO:0010592
positive regulation of lamellipodium assembly
|
IEA
GO_REF:0000107 |
ACCEPT |
Summary: positive regulation of lamellipodium assembly is consistent with core Cdc42 GTPase, cytoskeletal, polarity, or localization biology.
Reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane localization, or immediate actin/polarity outputs.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
CDC42 is directly linked to actin nucleation pathways through **WASP-family nucleation-promoting factors**.
|
|
GO:0015630
microtubule cytoskeleton
|
IEA
GO_REF:0000107 |
KEEP AS NON CORE |
Summary: microtubule cytoskeleton is a supported context-specific Cdc42 output.
Reason: Cdc42 controls broad cellular architecture and developmental programs through actin, polarity, trafficking, and kinase-effector pathways, but this term is not the core molecular function.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
In its **GTP-bound state**, CDC42 binds effector proteins that drive downstream cytoskeletal and polarity responses
|
|
GO:0016020
membrane
|
IEA
GO_REF:0000107 |
ACCEPT |
Summary: membrane is consistent with core Cdc42 GTPase, cytoskeletal, polarity, or localization biology.
Reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane localization, or immediate actin/polarity outputs.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
CDC42 associates with the **plasma membrane/cell cortex** via a **carboxy-terminal prenyl group**
|
|
GO:0017119
Golgi transport complex
|
IEA
GO_REF:0000107 |
KEEP AS NON CORE |
Summary: Golgi transport complex is a supported context-specific Cdc42 output.
Reason: Cdc42 controls broad cellular architecture and developmental programs through actin, polarity, trafficking, and kinase-effector pathways, but this term is not the core molecular function.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
In its **GTP-bound state**, CDC42 binds effector proteins that drive downstream cytoskeletal and polarity responses
|
|
GO:0019901
protein kinase binding
|
IEA
GO_REF:0000120 |
ACCEPT |
Summary: protein kinase binding is consistent with core Cdc42 GTPase, cytoskeletal, polarity, or localization biology.
Reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane localization, or immediate actin/polarity outputs.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
CDC42 is directly linked to actin nucleation pathways through **WASP-family nucleation-promoting factors**.
|
|
GO:0030036
actin cytoskeleton organization
|
IEA
GO_REF:0000107 |
ACCEPT |
Summary: actin cytoskeleton organization is consistent with core Cdc42 GTPase, cytoskeletal, polarity, or localization biology.
Reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane localization, or immediate actin/polarity outputs.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
CDC42 is directly linked to actin nucleation pathways through **WASP-family nucleation-promoting factors**.
|
|
GO:0030175
filopodium
|
IEA
GO_REF:0000107 |
ACCEPT |
Summary: filopodium is consistent with core Cdc42 GTPase, cytoskeletal, polarity, or localization biology.
Reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane localization, or immediate actin/polarity outputs.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
CDC42 is directly linked to actin nucleation pathways through **WASP-family nucleation-promoting factors**.
|
|
GO:0030307
positive regulation of cell growth
|
IEA
GO_REF:0000107 |
KEEP AS NON CORE |
Summary: positive regulation of cell growth is a supported context-specific Cdc42 output.
Reason: Cdc42 controls broad cellular architecture and developmental programs through actin, polarity, trafficking, and kinase-effector pathways, but this term is not the core molecular function.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
In its **GTP-bound state**, CDC42 binds effector proteins that drive downstream cytoskeletal and polarity responses
|
|
GO:0030335
positive regulation of cell migration
|
IEA
GO_REF:0000107 |
KEEP AS NON CORE |
Summary: positive regulation of cell migration is a supported context-specific Cdc42 output.
Reason: Cdc42 controls broad cellular architecture and developmental programs through actin, polarity, trafficking, and kinase-effector pathways, but this term is not the core molecular function.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
In its **GTP-bound state**, CDC42 binds effector proteins that drive downstream cytoskeletal and polarity responses
|
|
GO:0031274
positive regulation of pseudopodium assembly
|
IEA
GO_REF:0000107 |
ACCEPT |
Summary: positive regulation of pseudopodium assembly is consistent with core Cdc42 GTPase, cytoskeletal, polarity, or localization biology.
Reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane localization, or immediate actin/polarity outputs.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
CDC42 is directly linked to actin nucleation pathways through **WASP-family nucleation-promoting factors**.
|
|
GO:0031333
negative regulation of protein-containing complex assembly
|
IEA
GO_REF:0000107 |
KEEP AS NON CORE |
Summary: negative regulation of protein-containing complex assembly is a supported context-specific Cdc42 output.
Reason: Cdc42 controls broad cellular architecture and developmental programs through actin, polarity, trafficking, and kinase-effector pathways, but this term is not the core molecular function.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
In its **GTP-bound state**, CDC42 binds effector proteins that drive downstream cytoskeletal and polarity responses
|
|
GO:0031996
thioesterase binding
|
IEA
GO_REF:0000107 |
KEEP AS NON CORE |
Summary: thioesterase binding is a supported context-specific Cdc42 output.
Reason: Cdc42 controls broad cellular architecture and developmental programs through actin, polarity, trafficking, and kinase-effector pathways, but this term is not the core molecular function.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
In its **GTP-bound state**, CDC42 binds effector proteins that drive downstream cytoskeletal and polarity responses
|
|
GO:0032427
GBD domain binding
|
IEA
GO_REF:0000107 |
ACCEPT |
Summary: GBD domain binding is consistent with core Cdc42 GTPase, cytoskeletal, polarity, or localization biology.
Reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane localization, or immediate actin/polarity outputs.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
CDC42 is directly linked to actin nucleation pathways through **WASP-family nucleation-promoting factors**.
|
|
GO:0032467
positive regulation of cytokinesis
|
IEA
GO_REF:0000107 |
ACCEPT |
Summary: positive regulation of cytokinesis is supported for Cdc42, but this is a cell-cycle output rather than the small GTPase catalytic role itself.
Reason: UniProt carries this transferred process annotation, but it is treated as a downstream cell-cycle output rather than core GTPase catalysis.
Supporting Evidence:
UniProt:P60766
GO; GO:0032467; P:positive regulation of cytokinesis; ISS:UniProtKB.
|
|
GO:0032956
regulation of actin cytoskeleton organization
|
IEA
GO_REF:0000107 |
KEEP AS NON CORE |
Summary: regulation of actin cytoskeleton organization is a supported context-specific Cdc42 output.
Reason: Cdc42 controls broad cellular architecture and developmental programs through actin, polarity, trafficking, and kinase-effector pathways, but this term is not the core molecular function.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
In its **GTP-bound state**, CDC42 binds effector proteins that drive downstream cytoskeletal and polarity responses
|
|
GO:0032991
protein-containing complex
|
IEA
GO_REF:0000107 |
KEEP AS NON CORE |
Summary: protein-containing complex is a supported context-specific Cdc42 output.
Reason: Cdc42 controls broad cellular architecture and developmental programs through actin, polarity, trafficking, and kinase-effector pathways, but this term is not the core molecular function.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
In its **GTP-bound state**, CDC42 binds effector proteins that drive downstream cytoskeletal and polarity responses
|
|
GO:0034191
apolipoprotein A-I receptor binding
|
IEA
GO_REF:0000107 |
KEEP AS NON CORE |
Summary: apolipoprotein A-I receptor binding is a supported context-specific Cdc42 output.
Reason: Cdc42 controls broad cellular architecture and developmental programs through actin, polarity, trafficking, and kinase-effector pathways, but this term is not the core molecular function.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
In its **GTP-bound state**, CDC42 binds effector proteins that drive downstream cytoskeletal and polarity responses
|
|
GO:0034329
cell junction assembly
|
IEA
GO_REF:0000107 |
KEEP AS NON CORE |
Summary: cell junction assembly is a supported context-specific Cdc42 output.
Reason: Cdc42 controls broad cellular architecture and developmental programs through actin, polarity, trafficking, and kinase-effector pathways, but this term is not the core molecular function.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
In its **GTP-bound state**, CDC42 binds effector proteins that drive downstream cytoskeletal and polarity responses
|
|
GO:0036464
cytoplasmic ribonucleoprotein granule
|
IEA
GO_REF:0000107 |
KEEP AS NON CORE |
Summary: cytoplasmic ribonucleoprotein granule is retained as a non-core Cdc42-associated annotation.
Reason: The annotation is plausible as a downstream or compartment-specific consequence of Cdc42 signaling rather than the core GTPase switch activity.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
In its **GTP-bound state**, CDC42 binds effector proteins that drive downstream cytoskeletal and polarity responses
|
|
GO:0038189
neuropilin signaling pathway
|
IEA
GO_REF:0000107 |
KEEP AS NON CORE |
Summary: neuropilin signaling pathway is a supported context-specific Cdc42 output.
Reason: Cdc42 controls broad cellular architecture and developmental programs through actin, polarity, trafficking, and kinase-effector pathways, but this term is not the core molecular function.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
In its **GTP-bound state**, CDC42 binds effector proteins that drive downstream cytoskeletal and polarity responses
|
|
GO:0042802
identical protein binding
|
IEA
GO_REF:0000107 |
KEEP AS NON CORE |
Summary: identical protein binding is a supported context-specific Cdc42 output.
Reason: Cdc42 controls broad cellular architecture and developmental programs through actin, polarity, trafficking, and kinase-effector pathways, but this term is not the core molecular function.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
In its **GTP-bound state**, CDC42 binds effector proteins that drive downstream cytoskeletal and polarity responses
|
|
GO:0043005
neuron projection
|
IEA
GO_REF:0000107 |
KEEP AS NON CORE |
Summary: neuron projection is a supported context-specific Cdc42 output.
Reason: Cdc42 controls broad cellular architecture and developmental programs through actin, polarity, trafficking, and kinase-effector pathways, but this term is not the core molecular function.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
In its **GTP-bound state**, CDC42 binds effector proteins that drive downstream cytoskeletal and polarity responses
|
|
GO:0043025
neuronal cell body
|
IEA
GO_REF:0000107 |
KEEP AS NON CORE |
Summary: neuronal cell body is a supported context-specific Cdc42 output.
Reason: Cdc42 controls broad cellular architecture and developmental programs through actin, polarity, trafficking, and kinase-effector pathways, but this term is not the core molecular function.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
In its **GTP-bound state**, CDC42 binds effector proteins that drive downstream cytoskeletal and polarity responses
|
|
GO:0044788
host-mediated perturbation of viral process
|
IEA
GO_REF:0000107 |
KEEP AS NON CORE |
Summary: host-mediated perturbation of viral process is a supported context-specific Cdc42 output.
Reason: Cdc42 controls broad cellular architecture and developmental programs through actin, polarity, trafficking, and kinase-effector pathways, but this term is not the core molecular function.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
In its **GTP-bound state**, CDC42 binds effector proteins that drive downstream cytoskeletal and polarity responses
|
|
GO:0045198
establishment of epithelial cell apical/basal polarity
|
IEA
GO_REF:0000107 |
ACCEPT |
Summary: establishment of epithelial cell apical/basal polarity is consistent with core Cdc42 GTPase, cytoskeletal, polarity, or localization biology.
Reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane localization, or immediate actin/polarity outputs.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
In its **GTP-bound state**, CDC42 binds effector proteins that drive downstream cytoskeletal and polarity responses
|
|
GO:0051233
spindle midzone
|
IEA
GO_REF:0000107 |
ACCEPT |
Summary: spindle midzone is consistent with core Cdc42 GTPase, cytoskeletal, polarity, or localization biology.
Reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane localization, or immediate actin/polarity outputs.
Supporting Evidence:
UniProt:P60766
Moves to the central spindle as cells progressed through anaphase to telophase.
|
|
GO:0051489
regulation of filopodium assembly
|
IEA
GO_REF:0000107 |
ACCEPT |
Summary: regulation of filopodium assembly is consistent with core Cdc42 GTPase, cytoskeletal, polarity, or localization biology.
Reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane localization, or immediate actin/polarity outputs.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
CDC42 is directly linked to actin nucleation pathways through **WASP-family nucleation-promoting factors**.
|
|
GO:0051491
positive regulation of filopodium assembly
|
IEA
GO_REF:0000107 |
ACCEPT |
Summary: positive regulation of filopodium assembly is consistent with core Cdc42 GTPase, cytoskeletal, polarity, or localization biology.
Reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane localization, or immediate actin/polarity outputs.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
CDC42 is directly linked to actin nucleation pathways through **WASP-family nucleation-promoting factors**.
|
|
GO:0051492
regulation of stress fiber assembly
|
IEA
GO_REF:0000107 |
MODIFY |
Summary: The stress-fiber wording is too specific for the available Cdc42 evidence; the supported biology is broader actin organization through Cdc42 effector pathways.
Reason: Use a broader actin-organization term rather than treating stress-fiber assembly as a core Cdc42 output.
Proposed replacements:
actin filament organization
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
CDC42 is directly linked to actin nucleation pathways through **WASP-family nucleation-promoting factors**.
|
|
GO:0051496
positive regulation of stress fiber assembly
|
IEA
GO_REF:0000107 |
MODIFY |
Summary: The stress-fiber wording is too specific for the available Cdc42 evidence; the supported biology is broader actin organization through Cdc42 effector pathways.
Reason: Use a broader actin-organization term rather than treating stress-fiber assembly as a core Cdc42 output.
Proposed replacements:
actin filament organization
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
CDC42 is directly linked to actin nucleation pathways through **WASP-family nucleation-promoting factors**.
|
|
GO:0051988
regulation of attachment of spindle microtubules to kinetochore
|
IEA
GO_REF:0000107 |
ACCEPT |
Summary: regulation of attachment of spindle microtubules to kinetochore is consistent with core Cdc42 GTPase, cytoskeletal, polarity, or localization biology.
Reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane localization, or immediate actin/polarity outputs.
Supporting Evidence:
UniProt:P60766
Regulates the bipolar attachment of spindle microtubules to kinetochores before chromosome congression in metaphase.
|
|
GO:0061630
ubiquitin protein ligase activity
|
IEA
GO_REF:0000107 |
REMOVE |
Summary: Cdc42 is a small GTPase, not a ubiquitin-protein ligase.
Reason: No direct evidence supports assigning E3 ligase catalytic activity to Cdc42; this appears to be an over-transfer from associated pathways or interactors.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
CDC42 is a **GTP-hydrolyzing enzyme** (small GTPase). Its substrate is **GTP**, which it binds and hydrolyzes to **GDP + Pi**
|
|
GO:0072686
mitotic spindle
|
IEA
GO_REF:0000107 |
ACCEPT |
Summary: mitotic spindle is consistent with core Cdc42 GTPase, cytoskeletal, polarity, or localization biology.
Reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane localization, or immediate actin/polarity outputs.
Supporting Evidence:
UniProt:P60766
Cytoplasm, cytoskeleton, spindle
|
|
GO:1900026
positive regulation of substrate adhesion-dependent cell spreading
|
IEA
GO_REF:0000107 |
KEEP AS NON CORE |
Summary: positive regulation of substrate adhesion-dependent cell spreading is a supported context-specific Cdc42 output.
Reason: Cdc42 controls broad cellular architecture and developmental programs through actin, polarity, trafficking, and kinase-effector pathways, but this term is not the core molecular function.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
In its **GTP-bound state**, CDC42 binds effector proteins that drive downstream cytoskeletal and polarity responses
|
|
GO:0015630
microtubule cytoskeleton
|
ISO
GO_REF:0000119 |
KEEP AS NON CORE |
Summary: microtubule cytoskeleton is a supported context-specific Cdc42 output.
Reason: Cdc42 controls broad cellular architecture and developmental programs through actin, polarity, trafficking, and kinase-effector pathways, but this term is not the core molecular function.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
In its **GTP-bound state**, CDC42 binds effector proteins that drive downstream cytoskeletal and polarity responses
|
|
GO:0043085
positive regulation of catalytic activity
|
ISO
GO_REF:0000096 |
MODIFY |
Summary: positive regulation of catalytic activity is a broad ancestor for the Cdc42 signaling role.
Reason: Cdc42 is best represented as a small GTPase/Rho-family signaling switch.
Proposed replacements:
small GTPase-mediated signal transduction
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
CDC42 belongs to the **Rho family** of small GTPases and acts as a **molecular switch** cycling between **GTP-bound (active)** and **GDP-bound (inactive)** states
|
|
GO:0000139
Golgi membrane
|
ISO
GO_REF:0000096 |
KEEP AS NON CORE |
Summary: Golgi membrane is a supported context-specific Cdc42 output.
Reason: Cdc42 controls broad cellular architecture and developmental programs through actin, polarity, trafficking, and kinase-effector pathways, but this term is not the core molecular function.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
In its **GTP-bound state**, CDC42 binds effector proteins that drive downstream cytoskeletal and polarity responses
|
|
GO:0002040
sprouting angiogenesis
|
ISO
GO_REF:0000096 |
KEEP AS NON CORE |
Summary: sprouting angiogenesis is a supported context-specific Cdc42 output.
Reason: Cdc42 controls broad cellular architecture and developmental programs through actin, polarity, trafficking, and kinase-effector pathways, but this term is not the core molecular function.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
In its **GTP-bound state**, CDC42 binds effector proteins that drive downstream cytoskeletal and polarity responses
|
|
GO:0003924
GTPase activity
|
ISO
GO_REF:0000119 |
ACCEPT |
Summary: GTPase activity is consistent with core Cdc42 GTPase, cytoskeletal, polarity, or localization biology.
Reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane localization, or immediate actin/polarity outputs.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
CDC42 is a **GTP-hydrolyzing enzyme** (small GTPase). Its substrate is **GTP**, which it binds and hydrolyzes to **GDP + Pi**
|
|
GO:0005525
GTP binding
|
ISO
GO_REF:0000096 |
ACCEPT |
Summary: GTP binding is consistent with core Cdc42 GTPase, cytoskeletal, polarity, or localization biology.
Reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane localization, or immediate actin/polarity outputs.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
CDC42 is a **GTP-hydrolyzing enzyme** (small GTPase). Its substrate is **GTP**, which it binds and hydrolyzes to **GDP + Pi**
|
|
GO:0005525
GTP binding
|
ISO
GO_REF:0000119 |
ACCEPT |
Summary: GTP binding is consistent with core Cdc42 GTPase, cytoskeletal, polarity, or localization biology.
Reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane localization, or immediate actin/polarity outputs.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
CDC42 is a **GTP-hydrolyzing enzyme** (small GTPase). Its substrate is **GTP**, which it binds and hydrolyzes to **GDP + Pi**
|
|
GO:0005737
cytoplasm
|
ISO
GO_REF:0000119 |
ACCEPT |
Summary: cytoplasm is consistent with core Cdc42 GTPase, cytoskeletal, polarity, or localization biology.
Reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane localization, or immediate actin/polarity outputs.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
CDC42 associates with the **plasma membrane/cell cortex** via a **carboxy-terminal prenyl group**
|
|
GO:0005813
centrosome
|
ISO
GO_REF:0000119 |
ACCEPT |
Summary: centrosome is consistent with core Cdc42 GTPase, cytoskeletal, polarity, or localization biology.
Reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane localization, or immediate actin/polarity outputs.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
CDC42 is directly linked to actin nucleation pathways through **WASP-family nucleation-promoting factors**.
|
|
GO:0005886
plasma membrane
|
ISO
GO_REF:0000096 |
ACCEPT |
Summary: plasma membrane is consistent with core Cdc42 GTPase, cytoskeletal, polarity, or localization biology.
Reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane localization, or immediate actin/polarity outputs.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
CDC42 associates with the **plasma membrane/cell cortex** via a **carboxy-terminal prenyl group**
|
|
GO:0005886
plasma membrane
|
ISO
GO_REF:0000119 |
ACCEPT |
Summary: plasma membrane is consistent with core Cdc42 GTPase, cytoskeletal, polarity, or localization biology.
Reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane localization, or immediate actin/polarity outputs.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
CDC42 associates with the **plasma membrane/cell cortex** via a **carboxy-terminal prenyl group**
|
|
GO:0006911
phagocytosis, engulfment
|
ISO
GO_REF:0000119 |
ACCEPT |
Summary: phagocytosis, engulfment is consistent with core Cdc42 GTPase, cytoskeletal, polarity, or localization biology.
Reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane localization, or immediate actin/polarity outputs.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
CDC42 is directly linked to actin nucleation pathways through **WASP-family nucleation-promoting factors**.
|
|
GO:0007015
actin filament organization
|
ISO
GO_REF:0000096 |
ACCEPT |
Summary: actin filament organization is consistent with core Cdc42 GTPase, cytoskeletal, polarity, or localization biology.
Reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane localization, or immediate actin/polarity outputs.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
CDC42 is directly linked to actin nucleation pathways through **WASP-family nucleation-promoting factors**.
|
|
GO:0007015
actin filament organization
|
ISO
GO_REF:0000119 |
ACCEPT |
Summary: actin filament organization is consistent with core Cdc42 GTPase, cytoskeletal, polarity, or localization biology.
Reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane localization, or immediate actin/polarity outputs.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
CDC42 is directly linked to actin nucleation pathways through **WASP-family nucleation-promoting factors**.
|
|
GO:0007030
Golgi organization
|
ISO
GO_REF:0000096 |
KEEP AS NON CORE |
Summary: Golgi organization is a supported context-specific Cdc42 output.
Reason: Cdc42 controls broad cellular architecture and developmental programs through actin, polarity, trafficking, and kinase-effector pathways, but this term is not the core molecular function.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
In its **GTP-bound state**, CDC42 binds effector proteins that drive downstream cytoskeletal and polarity responses
|
|
GO:0007229
integrin-mediated signaling pathway
|
ISO
GO_REF:0000119 |
KEEP AS NON CORE |
Summary: integrin-mediated signaling pathway is a supported context-specific Cdc42 output.
Reason: Cdc42 controls broad cellular architecture and developmental programs through actin, polarity, trafficking, and kinase-effector pathways, but this term is not the core molecular function.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
In its **GTP-bound state**, CDC42 binds effector proteins that drive downstream cytoskeletal and polarity responses
|
|
GO:0010591
regulation of lamellipodium assembly
|
ISO
GO_REF:0000119 |
ACCEPT |
Summary: regulation of lamellipodium assembly is consistent with core Cdc42 GTPase, cytoskeletal, polarity, or localization biology.
Reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane localization, or immediate actin/polarity outputs.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
CDC42 is directly linked to actin nucleation pathways through **WASP-family nucleation-promoting factors**.
|
|
GO:0010592
positive regulation of lamellipodium assembly
|
ISO
GO_REF:0000119 |
ACCEPT |
Summary: positive regulation of lamellipodium assembly is consistent with core Cdc42 GTPase, cytoskeletal, polarity, or localization biology.
Reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane localization, or immediate actin/polarity outputs.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
CDC42 is directly linked to actin nucleation pathways through **WASP-family nucleation-promoting factors**.
|
|
GO:0016020
membrane
|
ISO
GO_REF:0000119 |
ACCEPT |
Summary: membrane is consistent with core Cdc42 GTPase, cytoskeletal, polarity, or localization biology.
Reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane localization, or immediate actin/polarity outputs.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
CDC42 associates with the **plasma membrane/cell cortex** via a **carboxy-terminal prenyl group**
|
|
GO:0017119
Golgi transport complex
|
ISO
GO_REF:0000119 |
KEEP AS NON CORE |
Summary: Golgi transport complex is a supported context-specific Cdc42 output.
Reason: Cdc42 controls broad cellular architecture and developmental programs through actin, polarity, trafficking, and kinase-effector pathways, but this term is not the core molecular function.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
In its **GTP-bound state**, CDC42 binds effector proteins that drive downstream cytoskeletal and polarity responses
|
|
GO:0019901
protein kinase binding
|
ISO
GO_REF:0000119 |
ACCEPT |
Summary: protein kinase binding is consistent with core Cdc42 GTPase, cytoskeletal, polarity, or localization biology.
Reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane localization, or immediate actin/polarity outputs.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
CDC42 is directly linked to actin nucleation pathways through **WASP-family nucleation-promoting factors**.
|
|
GO:0030036
actin cytoskeleton organization
|
ISO
GO_REF:0000119 |
ACCEPT |
Summary: actin cytoskeleton organization is consistent with core Cdc42 GTPase, cytoskeletal, polarity, or localization biology.
Reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane localization, or immediate actin/polarity outputs.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
CDC42 is directly linked to actin nucleation pathways through **WASP-family nucleation-promoting factors**.
|
|
GO:0030141
secretory granule
|
ISO
GO_REF:0000096 |
KEEP AS NON CORE |
Summary: secretory granule is a supported context-specific Cdc42 output.
Reason: Cdc42 controls broad cellular architecture and developmental programs through actin, polarity, trafficking, and kinase-effector pathways, but this term is not the core molecular function.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
In its **GTP-bound state**, CDC42 binds effector proteins that drive downstream cytoskeletal and polarity responses
|
|
GO:0030175
filopodium
|
ISO
GO_REF:0000119 |
ACCEPT |
Summary: filopodium is consistent with core Cdc42 GTPase, cytoskeletal, polarity, or localization biology.
Reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane localization, or immediate actin/polarity outputs.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
CDC42 is directly linked to actin nucleation pathways through **WASP-family nucleation-promoting factors**.
|
|
GO:0030307
positive regulation of cell growth
|
ISO
GO_REF:0000119 |
KEEP AS NON CORE |
Summary: positive regulation of cell growth is a supported context-specific Cdc42 output.
Reason: Cdc42 controls broad cellular architecture and developmental programs through actin, polarity, trafficking, and kinase-effector pathways, but this term is not the core molecular function.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
In its **GTP-bound state**, CDC42 binds effector proteins that drive downstream cytoskeletal and polarity responses
|
|
GO:0030335
positive regulation of cell migration
|
ISO
GO_REF:0000119 |
KEEP AS NON CORE |
Summary: positive regulation of cell migration is a supported context-specific Cdc42 output.
Reason: Cdc42 controls broad cellular architecture and developmental programs through actin, polarity, trafficking, and kinase-effector pathways, but this term is not the core molecular function.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
In its **GTP-bound state**, CDC42 binds effector proteins that drive downstream cytoskeletal and polarity responses
|
|
GO:0030496
midbody
|
ISO
GO_REF:0000119 |
ACCEPT |
Summary: midbody is consistent with core Cdc42 GTPase, cytoskeletal, polarity, or localization biology.
Reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane localization, or immediate actin/polarity outputs.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
CDC42 is directly linked to actin nucleation pathways through **WASP-family nucleation-promoting factors**.
|
|
GO:0031274
positive regulation of pseudopodium assembly
|
ISO
GO_REF:0000119 |
ACCEPT |
Summary: positive regulation of pseudopodium assembly is consistent with core Cdc42 GTPase, cytoskeletal, polarity, or localization biology.
Reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane localization, or immediate actin/polarity outputs.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
CDC42 is directly linked to actin nucleation pathways through **WASP-family nucleation-promoting factors**.
|
|
GO:0031333
negative regulation of protein-containing complex assembly
|
ISO
GO_REF:0000119 |
KEEP AS NON CORE |
Summary: negative regulation of protein-containing complex assembly is a supported context-specific Cdc42 output.
Reason: Cdc42 controls broad cellular architecture and developmental programs through actin, polarity, trafficking, and kinase-effector pathways, but this term is not the core molecular function.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
In its **GTP-bound state**, CDC42 binds effector proteins that drive downstream cytoskeletal and polarity responses
|
|
GO:0031435
mitogen-activated protein kinase kinase kinase binding
|
ISO
GO_REF:0000096 |
ACCEPT |
Summary: mitogen-activated protein kinase kinase kinase binding is consistent with core Cdc42 GTPase, cytoskeletal, polarity, or localization biology.
Reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane localization, or immediate actin/polarity outputs.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
CDC42 is directly linked to actin nucleation pathways through **WASP-family nucleation-promoting factors**.
|
|
GO:0031996
thioesterase binding
|
ISO
GO_REF:0000119 |
KEEP AS NON CORE |
Summary: thioesterase binding is a supported context-specific Cdc42 output.
Reason: Cdc42 controls broad cellular architecture and developmental programs through actin, polarity, trafficking, and kinase-effector pathways, but this term is not the core molecular function.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
In its **GTP-bound state**, CDC42 binds effector proteins that drive downstream cytoskeletal and polarity responses
|
|
GO:0032427
GBD domain binding
|
ISO
GO_REF:0000119 |
ACCEPT |
Summary: GBD domain binding is consistent with core Cdc42 GTPase, cytoskeletal, polarity, or localization biology.
Reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane localization, or immediate actin/polarity outputs.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
CDC42 is directly linked to actin nucleation pathways through **WASP-family nucleation-promoting factors**.
|
|
GO:0032467
positive regulation of cytokinesis
|
ISO
GO_REF:0000119 |
ACCEPT |
Summary: positive regulation of cytokinesis is supported for Cdc42, but this is a cell-cycle output rather than the small GTPase catalytic role itself.
Reason: UniProt carries this transferred process annotation, but it is treated as a downstream cell-cycle output rather than core GTPase catalysis.
Supporting Evidence:
UniProt:P60766
GO; GO:0032467; P:positive regulation of cytokinesis; ISS:UniProtKB.
|
|
GO:0032956
regulation of actin cytoskeleton organization
|
ISO
GO_REF:0000119 |
KEEP AS NON CORE |
Summary: regulation of actin cytoskeleton organization is a supported context-specific Cdc42 output.
Reason: Cdc42 controls broad cellular architecture and developmental programs through actin, polarity, trafficking, and kinase-effector pathways, but this term is not the core molecular function.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
In its **GTP-bound state**, CDC42 binds effector proteins that drive downstream cytoskeletal and polarity responses
|
|
GO:0032991
protein-containing complex
|
ISO
GO_REF:0000119 |
KEEP AS NON CORE |
Summary: protein-containing complex is a supported context-specific Cdc42 output.
Reason: Cdc42 controls broad cellular architecture and developmental programs through actin, polarity, trafficking, and kinase-effector pathways, but this term is not the core molecular function.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
In its **GTP-bound state**, CDC42 binds effector proteins that drive downstream cytoskeletal and polarity responses
|
|
GO:0034191
apolipoprotein A-I receptor binding
|
ISO
GO_REF:0000119 |
KEEP AS NON CORE |
Summary: apolipoprotein A-I receptor binding is a supported context-specific Cdc42 output.
Reason: Cdc42 controls broad cellular architecture and developmental programs through actin, polarity, trafficking, and kinase-effector pathways, but this term is not the core molecular function.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
In its **GTP-bound state**, CDC42 binds effector proteins that drive downstream cytoskeletal and polarity responses
|
|
GO:0034329
cell junction assembly
|
ISO
GO_REF:0000119 |
KEEP AS NON CORE |
Summary: cell junction assembly is a supported context-specific Cdc42 output.
Reason: Cdc42 controls broad cellular architecture and developmental programs through actin, polarity, trafficking, and kinase-effector pathways, but this term is not the core molecular function.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
In its **GTP-bound state**, CDC42 binds effector proteins that drive downstream cytoskeletal and polarity responses
|
|
GO:0036464
cytoplasmic ribonucleoprotein granule
|
ISO
GO_REF:0000119 |
KEEP AS NON CORE |
Summary: cytoplasmic ribonucleoprotein granule is retained as a non-core Cdc42-associated annotation.
Reason: The annotation is plausible as a downstream or compartment-specific consequence of Cdc42 signaling rather than the core GTPase switch activity.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
In its **GTP-bound state**, CDC42 binds effector proteins that drive downstream cytoskeletal and polarity responses
|
|
GO:0038189
neuropilin signaling pathway
|
ISO
GO_REF:0000119 |
KEEP AS NON CORE |
Summary: neuropilin signaling pathway is a supported context-specific Cdc42 output.
Reason: Cdc42 controls broad cellular architecture and developmental programs through actin, polarity, trafficking, and kinase-effector pathways, but this term is not the core molecular function.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
In its **GTP-bound state**, CDC42 binds effector proteins that drive downstream cytoskeletal and polarity responses
|
|
GO:0042802
identical protein binding
|
ISO
GO_REF:0000119 |
KEEP AS NON CORE |
Summary: identical protein binding is a supported context-specific Cdc42 output.
Reason: Cdc42 controls broad cellular architecture and developmental programs through actin, polarity, trafficking, and kinase-effector pathways, but this term is not the core molecular function.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
In its **GTP-bound state**, CDC42 binds effector proteins that drive downstream cytoskeletal and polarity responses
|
|
GO:0043005
neuron projection
|
ISO
GO_REF:0000119 |
KEEP AS NON CORE |
Summary: neuron projection is a supported context-specific Cdc42 output.
Reason: Cdc42 controls broad cellular architecture and developmental programs through actin, polarity, trafficking, and kinase-effector pathways, but this term is not the core molecular function.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
In its **GTP-bound state**, CDC42 binds effector proteins that drive downstream cytoskeletal and polarity responses
|
|
GO:0043025
neuronal cell body
|
ISO
GO_REF:0000119 |
KEEP AS NON CORE |
Summary: neuronal cell body is a supported context-specific Cdc42 output.
Reason: Cdc42 controls broad cellular architecture and developmental programs through actin, polarity, trafficking, and kinase-effector pathways, but this term is not the core molecular function.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
In its **GTP-bound state**, CDC42 binds effector proteins that drive downstream cytoskeletal and polarity responses
|
|
GO:0043525
positive regulation of neuron apoptotic process
|
ISO
GO_REF:0000096 |
KEEP AS NON CORE |
Summary: positive regulation of neuron apoptotic process is a supported context-specific Cdc42 output.
Reason: Cdc42 controls broad cellular architecture and developmental programs through actin, polarity, trafficking, and kinase-effector pathways, but this term is not the core molecular function.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
In its **GTP-bound state**, CDC42 binds effector proteins that drive downstream cytoskeletal and polarity responses
|
|
GO:0044788
host-mediated perturbation of viral process
|
ISO
GO_REF:0000119 |
KEEP AS NON CORE |
Summary: host-mediated perturbation of viral process is a supported context-specific Cdc42 output.
Reason: Cdc42 controls broad cellular architecture and developmental programs through actin, polarity, trafficking, and kinase-effector pathways, but this term is not the core molecular function.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
In its **GTP-bound state**, CDC42 binds effector proteins that drive downstream cytoskeletal and polarity responses
|
|
GO:0045198
establishment of epithelial cell apical/basal polarity
|
ISO
GO_REF:0000119 |
ACCEPT |
Summary: establishment of epithelial cell apical/basal polarity is consistent with core Cdc42 GTPase, cytoskeletal, polarity, or localization biology.
Reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane localization, or immediate actin/polarity outputs.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
CDC42 is directly linked to actin nucleation pathways through **WASP-family nucleation-promoting factors**.
|
|
GO:0045740
positive regulation of DNA replication
|
ISO
GO_REF:0000096 |
KEEP AS NON CORE |
Summary: positive regulation of DNA replication is a supported context-specific Cdc42 output.
Reason: Cdc42 controls broad cellular architecture and developmental programs through actin, polarity, trafficking, and kinase-effector pathways, but this term is not the core molecular function.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
In its **GTP-bound state**, CDC42 binds effector proteins that drive downstream cytoskeletal and polarity responses
|
|
GO:0046330
positive regulation of JNK cascade
|
ISO
GO_REF:0000096 |
UNDECIDED |
Summary: The current local evidence supports context-specific Cdc42/p38 MAPK signaling, but does not establish a specific JNK cascade annotation.
Reason: Retaining this JNK-specific automated transfer requires direct term-specific evidence.
|
|
GO:0051233
spindle midzone
|
ISO
GO_REF:0000119 |
ACCEPT |
Summary: spindle midzone is consistent with core Cdc42 GTPase, cytoskeletal, polarity, or localization biology.
Reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane localization, or immediate actin/polarity outputs.
Supporting Evidence:
UniProt:P60766
Moves to the central spindle as cells progressed through anaphase to telophase.
|
|
GO:0051489
regulation of filopodium assembly
|
ISO
GO_REF:0000119 |
ACCEPT |
Summary: regulation of filopodium assembly is consistent with core Cdc42 GTPase, cytoskeletal, polarity, or localization biology.
Reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane localization, or immediate actin/polarity outputs.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
CDC42 is directly linked to actin nucleation pathways through **WASP-family nucleation-promoting factors**.
|
|
GO:0051491
positive regulation of filopodium assembly
|
ISO
GO_REF:0000119 |
ACCEPT |
Summary: positive regulation of filopodium assembly is consistent with core Cdc42 GTPase, cytoskeletal, polarity, or localization biology.
Reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane localization, or immediate actin/polarity outputs.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
CDC42 is directly linked to actin nucleation pathways through **WASP-family nucleation-promoting factors**.
|
|
GO:0051492
regulation of stress fiber assembly
|
ISO
GO_REF:0000119 |
MODIFY |
Summary: The stress-fiber wording is too specific for the available Cdc42 evidence; the supported biology is broader actin organization through Cdc42 effector pathways.
Reason: Use a broader actin-organization term rather than treating stress-fiber assembly as a core Cdc42 output.
Proposed replacements:
actin filament organization
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
CDC42 is directly linked to actin nucleation pathways through **WASP-family nucleation-promoting factors**.
|
|
GO:0051496
positive regulation of stress fiber assembly
|
ISO
GO_REF:0000119 |
MODIFY |
Summary: The stress-fiber wording is too specific for the available Cdc42 evidence; the supported biology is broader actin organization through Cdc42 effector pathways.
Reason: Use a broader actin-organization term rather than treating stress-fiber assembly as a core Cdc42 output.
Proposed replacements:
actin filament organization
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
CDC42 is directly linked to actin nucleation pathways through **WASP-family nucleation-promoting factors**.
|
|
GO:0051683
establishment of Golgi localization
|
ISO
GO_REF:0000096 |
KEEP AS NON CORE |
Summary: establishment of Golgi localization is a supported context-specific Cdc42 output.
Reason: Cdc42 controls broad cellular architecture and developmental programs through actin, polarity, trafficking, and kinase-effector pathways, but this term is not the core molecular function.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
In its **GTP-bound state**, CDC42 binds effector proteins that drive downstream cytoskeletal and polarity responses
|
|
GO:0051835
positive regulation of synapse structural plasticity
|
ISO
GO_REF:0000096 |
KEEP AS NON CORE |
Summary: positive regulation of synapse structural plasticity is a supported context-specific Cdc42 output.
Reason: Cdc42 controls broad cellular architecture and developmental programs through actin, polarity, trafficking, and kinase-effector pathways, but this term is not the core molecular function.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
In its **GTP-bound state**, CDC42 binds effector proteins that drive downstream cytoskeletal and polarity responses
|
|
GO:0051988
regulation of attachment of spindle microtubules to kinetochore
|
ISO
GO_REF:0000119 |
ACCEPT |
Summary: regulation of attachment of spindle microtubules to kinetochore is consistent with core Cdc42 GTPase, cytoskeletal, polarity, or localization biology.
Reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane localization, or immediate actin/polarity outputs.
Supporting Evidence:
UniProt:P60766
Regulates the bipolar attachment of spindle microtubules to kinetochores before chromosome congression in metaphase.
|
|
GO:0061630
ubiquitin protein ligase activity
|
ISO
GO_REF:0000119 |
REMOVE |
Summary: Cdc42 is a small GTPase, not a ubiquitin-protein ligase.
Reason: No direct evidence supports assigning E3 ligase catalytic activity to Cdc42; this appears to be an over-transfer from associated pathways or interactors.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
CDC42 is a **GTP-hydrolyzing enzyme** (small GTPase). Its substrate is **GTP**, which it binds and hydrolyzes to **GDP + Pi**
|
|
GO:0072384
organelle transport along microtubule
|
ISO
GO_REF:0000096 |
KEEP AS NON CORE |
Summary: organelle transport along microtubule is a supported context-specific Cdc42 output.
Reason: Cdc42 controls broad cellular architecture and developmental programs through actin, polarity, trafficking, and kinase-effector pathways, but this term is not the core molecular function.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
In its **GTP-bound state**, CDC42 binds effector proteins that drive downstream cytoskeletal and polarity responses
|
|
GO:0072686
mitotic spindle
|
ISO
GO_REF:0000119 |
ACCEPT |
Summary: mitotic spindle is consistent with core Cdc42 GTPase, cytoskeletal, polarity, or localization biology.
Reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane localization, or immediate actin/polarity outputs.
Supporting Evidence:
UniProt:P60766
Cytoplasm, cytoskeleton, spindle
|
|
GO:0090135
actin filament branching
|
ISO
GO_REF:0000096 |
ACCEPT |
Summary: actin filament branching is consistent with core Cdc42 GTPase, cytoskeletal, polarity, or localization biology.
Reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane localization, or immediate actin/polarity outputs.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
CDC42 is directly linked to actin nucleation pathways through **WASP-family nucleation-promoting factors**.
|
|
GO:0090316
positive regulation of intracellular protein transport
|
ISO
GO_REF:0000096 |
KEEP AS NON CORE |
Summary: positive regulation of intracellular protein transport is a supported context-specific Cdc42 output.
Reason: Cdc42 controls broad cellular architecture and developmental programs through actin, polarity, trafficking, and kinase-effector pathways, but this term is not the core molecular function.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
In its **GTP-bound state**, CDC42 binds effector proteins that drive downstream cytoskeletal and polarity responses
|
|
GO:0098685
Schaffer collateral - CA1 synapse
|
ISO
GO_REF:0000096 |
KEEP AS NON CORE |
Summary: Schaffer collateral - CA1 synapse is a supported context-specific Cdc42 output.
Reason: Cdc42 controls broad cellular architecture and developmental programs through actin, polarity, trafficking, and kinase-effector pathways, but this term is not the core molecular function.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
In its **GTP-bound state**, CDC42 binds effector proteins that drive downstream cytoskeletal and polarity responses
|
|
GO:0099159
regulation of modification of postsynaptic structure
|
ISO
GO_REF:0000096 |
KEEP AS NON CORE |
Summary: regulation of modification of postsynaptic structure is a supported context-specific Cdc42 output.
Reason: Cdc42 controls broad cellular architecture and developmental programs through actin, polarity, trafficking, and kinase-effector pathways, but this term is not the core molecular function.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
In its **GTP-bound state**, CDC42 binds effector proteins that drive downstream cytoskeletal and polarity responses
|
|
GO:1900026
positive regulation of substrate adhesion-dependent cell spreading
|
ISO
GO_REF:0000119 |
KEEP AS NON CORE |
Summary: positive regulation of substrate adhesion-dependent cell spreading is a supported context-specific Cdc42 output.
Reason: Cdc42 controls broad cellular architecture and developmental programs through actin, polarity, trafficking, and kinase-effector pathways, but this term is not the core molecular function.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
In its **GTP-bound state**, CDC42 binds effector proteins that drive downstream cytoskeletal and polarity responses
|
|
GO:0005515
protein binding
|
IPI
PMID:24076653 CDC42 switches IRSp53 from inhibition of actin growth to elo... |
MARK AS OVER ANNOTATED |
Summary: protein binding records a physical association but is too generic to describe the gene product function.
Reason: The evidence supports regulated signaling-complex assembly, not a meaningful standalone protein binding function; more informative molecular and pathway terms capture the biology.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
In its **GTP-bound state**, CDC42 binds effector proteins that drive downstream cytoskeletal and polarity responses
|
|
GO:0005515
protein binding
|
IPI
PMID:37140151 Biallelic variants in IQCN cause sperm flagellar assembly de... |
MARK AS OVER ANNOTATED |
Summary: protein binding records a physical association but is too generic to describe the gene product function.
Reason: The evidence supports regulated signaling-complex assembly, not a meaningful standalone protein binding function; more informative molecular and pathway terms capture the biology.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
In its **GTP-bound state**, CDC42 binds effector proteins that drive downstream cytoskeletal and polarity responses
|
|
GO:0098794
postsynapse
|
IDA
PMID:33531495 Photoactivatable CaMKII induces synaptic plasticity in singl... |
KEEP AS NON CORE |
Summary: postsynapse is a supported context-specific Cdc42 output.
Reason: Cdc42 controls broad cellular architecture and developmental programs through actin, polarity, trafficking, and kinase-effector pathways, but this term is not the core molecular function.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
In its **GTP-bound state**, CDC42 binds effector proteins that drive downstream cytoskeletal and polarity responses
|
|
GO:0098794
postsynapse
|
IMP
PMID:33531495 Photoactivatable CaMKII induces synaptic plasticity in singl... |
KEEP AS NON CORE |
Summary: postsynapse is a supported context-specific Cdc42 output.
Reason: Cdc42 controls broad cellular architecture and developmental programs through actin, polarity, trafficking, and kinase-effector pathways, but this term is not the core molecular function.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
In its **GTP-bound state**, CDC42 binds effector proteins that drive downstream cytoskeletal and polarity responses
|
|
GO:0098978
glutamatergic synapse
|
IDA
PMID:25851601 The RhoGEF DOCK10 is essential for dendritic spine morphogen... |
KEEP AS NON CORE |
Summary: glutamatergic synapse is a supported context-specific Cdc42 output.
Reason: Cdc42 controls broad cellular architecture and developmental programs through actin, polarity, trafficking, and kinase-effector pathways, but this term is not the core molecular function.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
In its **GTP-bound state**, CDC42 binds effector proteins that drive downstream cytoskeletal and polarity responses
|
|
GO:0098978
glutamatergic synapse
|
IMP
PMID:25851601 The RhoGEF DOCK10 is essential for dendritic spine morphogen... |
KEEP AS NON CORE |
Summary: glutamatergic synapse is a supported context-specific Cdc42 output.
Reason: Cdc42 controls broad cellular architecture and developmental programs through actin, polarity, trafficking, and kinase-effector pathways, but this term is not the core molecular function.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
In its **GTP-bound state**, CDC42 binds effector proteins that drive downstream cytoskeletal and polarity responses
|
|
GO:0098978
glutamatergic synapse
|
IDA
PMID:33531495 Photoactivatable CaMKII induces synaptic plasticity in singl... |
KEEP AS NON CORE |
Summary: glutamatergic synapse is a supported context-specific Cdc42 output.
Reason: Cdc42 controls broad cellular architecture and developmental programs through actin, polarity, trafficking, and kinase-effector pathways, but this term is not the core molecular function.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
In its **GTP-bound state**, CDC42 binds effector proteins that drive downstream cytoskeletal and polarity responses
|
|
GO:0098978
glutamatergic synapse
|
IMP
PMID:33531495 Photoactivatable CaMKII induces synaptic plasticity in singl... |
KEEP AS NON CORE |
Summary: glutamatergic synapse is a supported context-specific Cdc42 output.
Reason: Cdc42 controls broad cellular architecture and developmental programs through actin, polarity, trafficking, and kinase-effector pathways, but this term is not the core molecular function.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
In its **GTP-bound state**, CDC42 binds effector proteins that drive downstream cytoskeletal and polarity responses
|
|
GO:0099175
regulation of postsynapse organization
|
IDA
PMID:25851601 The RhoGEF DOCK10 is essential for dendritic spine morphogen... |
KEEP AS NON CORE |
Summary: regulation of postsynapse organization is a supported context-specific Cdc42 output.
Reason: Cdc42 controls broad cellular architecture and developmental programs through actin, polarity, trafficking, and kinase-effector pathways, but this term is not the core molecular function.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
In its **GTP-bound state**, CDC42 binds effector proteins that drive downstream cytoskeletal and polarity responses
|
|
GO:0099175
regulation of postsynapse organization
|
IMP
PMID:25851601 The RhoGEF DOCK10 is essential for dendritic spine morphogen... |
KEEP AS NON CORE |
Summary: regulation of postsynapse organization is a supported context-specific Cdc42 output.
Reason: Cdc42 controls broad cellular architecture and developmental programs through actin, polarity, trafficking, and kinase-effector pathways, but this term is not the core molecular function.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
In its **GTP-bound state**, CDC42 binds effector proteins that drive downstream cytoskeletal and polarity responses
|
|
GO:0003015
heart process
|
IMP
PMID:25197047 Essential role of sympathetic endothelin A receptors for adv... |
KEEP AS NON CORE |
Summary: heart process is a supported context-specific Cdc42 output.
Reason: Cdc42 controls broad cellular architecture and developmental programs through actin, polarity, trafficking, and kinase-effector pathways, but this term is not the core molecular function.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
In its **GTP-bound state**, CDC42 binds effector proteins that drive downstream cytoskeletal and polarity responses
|
|
GO:0003015
heart process
|
IMP
PMID:31219639 Cdc42 activation by endothelin regulates neural crest cell m... |
KEEP AS NON CORE |
Summary: heart process is a supported context-specific Cdc42 output.
Reason: Cdc42 controls broad cellular architecture and developmental programs through actin, polarity, trafficking, and kinase-effector pathways, but this term is not the core molecular function.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
In its **GTP-bound state**, CDC42 binds effector proteins that drive downstream cytoskeletal and polarity responses
|
|
GO:0003253
cardiac neural crest cell migration involved in outflow tract morphogenesis
|
IMP
PMID:31219639 Cdc42 activation by endothelin regulates neural crest cell m... |
KEEP AS NON CORE |
Summary: cardiac neural crest cell migration involved in outflow tract morphogenesis is a supported context-specific Cdc42 output.
Reason: Cdc42 controls broad cellular architecture and developmental programs through actin, polarity, trafficking, and kinase-effector pathways, but this term is not the core molecular function.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
In its **GTP-bound state**, CDC42 binds effector proteins that drive downstream cytoskeletal and polarity responses
|
|
GO:0006468
protein phosphorylation
|
IMP
PMID:31219639 Cdc42 activation by endothelin regulates neural crest cell m... |
MODIFY |
Summary: Cdc42 does not itself catalyze protein phosphorylation.
Reason: The evidence supports upstream small-GTPase signaling to kinase effectors such as PAK rather than direct kinase activity by Cdc42.
Proposed replacements:
small GTPase-mediated signal transduction
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
In its **GTP-bound state**, CDC42 binds effector proteins that drive downstream cytoskeletal and polarity responses
|
|
GO:0031252
cell leading edge
|
IDA
PMID:31219639 Cdc42 activation by endothelin regulates neural crest cell m... |
ACCEPT |
Summary: cell leading edge is consistent with core Cdc42 GTPase, cytoskeletal, polarity, or localization biology.
Reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane localization, or immediate actin/polarity outputs.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
CDC42 is directly linked to actin nucleation pathways through **WASP-family nucleation-promoting factors**.
|
|
GO:0035050
embryonic heart tube development
|
IMP
PMID:31219639 Cdc42 activation by endothelin regulates neural crest cell m... |
KEEP AS NON CORE |
Summary: embryonic heart tube development is a supported context-specific Cdc42 output.
Reason: Cdc42 controls broad cellular architecture and developmental programs through actin, polarity, trafficking, and kinase-effector pathways, but this term is not the core molecular function.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
In its **GTP-bound state**, CDC42 binds effector proteins that drive downstream cytoskeletal and polarity responses
|
|
GO:0086100
endothelin receptor signaling pathway
|
IMP
PMID:31219639 Cdc42 activation by endothelin regulates neural crest cell m... |
KEEP AS NON CORE |
Summary: endothelin receptor signaling pathway is retained as a non-core Cdc42-associated annotation.
Reason: The annotation is plausible as a downstream or compartment-specific consequence of Cdc42 signaling rather than the core GTPase switch activity.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
In its **GTP-bound state**, CDC42 binds effector proteins that drive downstream cytoskeletal and polarity responses
|
|
GO:0005515
protein binding
|
IPI
PMID:15710388 Zizimin2: a novel, DOCK180-related Cdc42 guanine nucleotide ... |
MARK AS OVER ANNOTATED |
Summary: protein binding records a physical association but is too generic to describe the gene product function.
Reason: The evidence supports regulated signaling-complex assembly, not a meaningful standalone protein binding function; more informative molecular and pathway terms capture the biology.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
In its **GTP-bound state**, CDC42 binds effector proteins that drive downstream cytoskeletal and polarity responses
|
|
GO:0005515
protein binding
|
IPI
PMID:18604197 IQGAP3 regulates cell proliferation through the Ras/ERK sign... |
MARK AS OVER ANNOTATED |
Summary: protein binding records a physical association but is too generic to describe the gene product function.
Reason: The evidence supports regulated signaling-complex assembly, not a meaningful standalone protein binding function; more informative molecular and pathway terms capture the biology.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
In its **GTP-bound state**, CDC42 binds effector proteins that drive downstream cytoskeletal and polarity responses
|
|
GO:0005515
protein binding
|
IPI
PMID:21828338 Cool-1/βPIX functions as a guanine nucleotide exchange facto... |
MARK AS OVER ANNOTATED |
Summary: protein binding records a physical association but is too generic to describe the gene product function.
Reason: The evidence supports regulated signaling-complex assembly, not a meaningful standalone protein binding function; more informative molecular and pathway terms capture the biology.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
In its **GTP-bound state**, CDC42 binds effector proteins that drive downstream cytoskeletal and polarity responses
|
|
GO:0005515
protein binding
|
IPI
PMID:8464478 Oncogene ect2 is related to regulators of small GTP-binding ... |
MARK AS OVER ANNOTATED |
Summary: protein binding records a physical association but is too generic to describe the gene product function.
Reason: The evidence supports regulated signaling-complex assembly, not a meaningful standalone protein binding function; more informative molecular and pathway terms capture the biology.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
In its **GTP-bound state**, CDC42 binds effector proteins that drive downstream cytoskeletal and polarity responses
|
|
GO:0003924
GTPase activity
|
ISO
PMID:27917469 Association of dysfunctional synapse defective 1 (SYDE1) wit... |
ACCEPT |
Summary: GTPase activity is consistent with core Cdc42 GTPase, cytoskeletal, polarity, or localization biology.
Reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane localization, or immediate actin/polarity outputs.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
CDC42 is a **GTP-hydrolyzing enzyme** (small GTPase). Its substrate is **GTP**, which it binds and hydrolyzes to **GDP + Pi**
|
|
GO:0048549
positive regulation of pinocytosis
|
IMP
PMID:24792215 CLN3 deficient cells display defects in the ARF1-Cdc42 pathw... |
ACCEPT |
Summary: positive regulation of pinocytosis is consistent with core Cdc42 GTPase, cytoskeletal, polarity, or localization biology.
Reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane localization, or immediate actin/polarity outputs.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
CDC42 is directly linked to actin nucleation pathways through **WASP-family nucleation-promoting factors**.
|
|
GO:0045335
phagocytic vesicle
|
IDA
PMID:19144319 The phagosomal proteome in interferon-gamma-activated macrop... |
ACCEPT |
Summary: phagocytic vesicle is consistent with core Cdc42 GTPase, cytoskeletal, polarity, or localization biology.
Reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane localization, or immediate actin/polarity outputs.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
CDC42 is directly linked to actin nucleation pathways through **WASP-family nucleation-promoting factors**.
|
|
GO:0071346
cellular response to type II interferon
|
IDA
PMID:19144319 The phagosomal proteome in interferon-gamma-activated macrop... |
KEEP AS NON CORE |
Summary: cellular response to type II interferon is a supported context-specific Cdc42 output.
Reason: Cdc42 controls broad cellular architecture and developmental programs through actin, polarity, trafficking, and kinase-effector pathways, but this term is not the core molecular function.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
In its **GTP-bound state**, CDC42 binds effector proteins that drive downstream cytoskeletal and polarity responses
|
|
GO:0006911
phagocytosis, engulfment
|
ISS
GO_REF:0000024 |
ACCEPT |
Summary: phagocytosis, engulfment is consistent with core Cdc42 GTPase, cytoskeletal, polarity, or localization biology.
Reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane localization, or immediate actin/polarity outputs.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
CDC42 is directly linked to actin nucleation pathways through **WASP-family nucleation-promoting factors**.
|
|
GO:0007015
actin filament organization
|
ISS
GO_REF:0000024 |
ACCEPT |
Summary: actin filament organization is consistent with core Cdc42 GTPase, cytoskeletal, polarity, or localization biology.
Reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane localization, or immediate actin/polarity outputs.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
CDC42 is directly linked to actin nucleation pathways through **WASP-family nucleation-promoting factors**.
|
|
GO:0034329
cell junction assembly
|
ISS
GO_REF:0000024 |
KEEP AS NON CORE |
Summary: cell junction assembly is a supported context-specific Cdc42 output.
Reason: Cdc42 controls broad cellular architecture and developmental programs through actin, polarity, trafficking, and kinase-effector pathways, but this term is not the core molecular function.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
In its **GTP-bound state**, CDC42 binds effector proteins that drive downstream cytoskeletal and polarity responses
|
|
GO:0045198
establishment of epithelial cell apical/basal polarity
|
ISS
GO_REF:0000024 |
ACCEPT |
Summary: establishment of epithelial cell apical/basal polarity is consistent with core Cdc42 GTPase, cytoskeletal, polarity, or localization biology.
Reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane localization, or immediate actin/polarity outputs.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
CDC42 is directly linked to actin nucleation pathways through **WASP-family nucleation-promoting factors**.
|
|
GO:0051491
positive regulation of filopodium assembly
|
IMP
PMID:22494997 Age-related guanine nucleotide exchange factor, mouse Zizimi... |
ACCEPT |
Summary: positive regulation of filopodium assembly is consistent with core Cdc42 GTPase, cytoskeletal, polarity, or localization biology.
Reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane localization, or immediate actin/polarity outputs.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
CDC42 is directly linked to actin nucleation pathways through **WASP-family nucleation-promoting factors**.
|
|
GO:0060997
dendritic spine morphogenesis
|
IMP
PMID:25851601 The RhoGEF DOCK10 is essential for dendritic spine morphogen... |
KEEP AS NON CORE |
Summary: dendritic spine morphogenesis is a supported context-specific Cdc42 output.
Reason: Cdc42 controls broad cellular architecture and developmental programs through actin, polarity, trafficking, and kinase-effector pathways, but this term is not the core molecular function.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
In its **GTP-bound state**, CDC42 binds effector proteins that drive downstream cytoskeletal and polarity responses
|
|
GO:0003924
GTPase activity
|
IDA
PMID:18838382 FGD2, a CDC42-specific exchange factor expressed by antigen-... |
ACCEPT |
Summary: GTPase activity is consistent with core Cdc42 GTPase, cytoskeletal, polarity, or localization biology.
Reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane localization, or immediate actin/polarity outputs.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
CDC42 is a **GTP-hydrolyzing enzyme** (small GTPase). Its substrate is **GTP**, which it binds and hydrolyzes to **GDP + Pi**
|
|
GO:0003924
GTPase activity
|
IGI
PMID:18838382 FGD2, a CDC42-specific exchange factor expressed by antigen-... |
ACCEPT |
Summary: GTPase activity is consistent with core Cdc42 GTPase, cytoskeletal, polarity, or localization biology.
Reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane localization, or immediate actin/polarity outputs.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
CDC42 is a **GTP-hydrolyzing enzyme** (small GTPase). Its substrate is **GTP**, which it binds and hydrolyzes to **GDP + Pi**
|
|
GO:0005515
protein binding
|
IPI
PMID:18838382 FGD2, a CDC42-specific exchange factor expressed by antigen-... |
MARK AS OVER ANNOTATED |
Summary: protein binding records a physical association but is too generic to describe the gene product function.
Reason: The evidence supports regulated signaling-complex assembly, not a meaningful standalone protein binding function; more informative molecular and pathway terms capture the biology.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
In its **GTP-bound state**, CDC42 binds effector proteins that drive downstream cytoskeletal and polarity responses
|
|
GO:0000322
storage vacuole
|
IDA
PMID:21828338 Cool-1/βPIX functions as a guanine nucleotide exchange facto... |
KEEP AS NON CORE |
Summary: storage vacuole is a supported context-specific Cdc42 output.
Reason: Cdc42 controls broad cellular architecture and developmental programs through actin, polarity, trafficking, and kinase-effector pathways, but this term is not the core molecular function.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
In its **GTP-bound state**, CDC42 binds effector proteins that drive downstream cytoskeletal and polarity responses
|
|
GO:0005829
cytosol
|
IDA
PMID:21828338 Cool-1/βPIX functions as a guanine nucleotide exchange facto... |
ACCEPT |
Summary: cytosol is consistent with core Cdc42 GTPase, cytoskeletal, polarity, or localization biology.
Reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane localization, or immediate actin/polarity outputs.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
CDC42 associates with the **plasma membrane/cell cortex** via a **carboxy-terminal prenyl group**
|
|
GO:0005886
plasma membrane
|
IDA
PMID:21828338 Cool-1/βPIX functions as a guanine nucleotide exchange facto... |
ACCEPT |
Summary: plasma membrane is consistent with core Cdc42 GTPase, cytoskeletal, polarity, or localization biology.
Reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane localization, or immediate actin/polarity outputs.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
CDC42 associates with the **plasma membrane/cell cortex** via a **carboxy-terminal prenyl group**
|
|
GO:0005886
plasma membrane
|
IDA
PMID:25217619 Phosphoinositide 3-kinase p85beta regulates invadopodium for... |
ACCEPT |
Summary: plasma membrane is consistent with core Cdc42 GTPase, cytoskeletal, polarity, or localization biology.
Reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane localization, or immediate actin/polarity outputs.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
CDC42 associates with the **plasma membrane/cell cortex** via a **carboxy-terminal prenyl group**
|
|
GO:0005886
plasma membrane
|
TAS
Reactome:R-MMU-3928643 |
ACCEPT |
Summary: plasma membrane is consistent with core Cdc42 GTPase, cytoskeletal, polarity, or localization biology.
Reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane localization, or immediate actin/polarity outputs.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
CDC42 associates with the **plasma membrane/cell cortex** via a **carboxy-terminal prenyl group**
|
|
GO:0005886
plasma membrane
|
TAS
Reactome:R-MMU-442572 |
ACCEPT |
Summary: plasma membrane is consistent with core Cdc42 GTPase, cytoskeletal, polarity, or localization biology.
Reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane localization, or immediate actin/polarity outputs.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
CDC42 associates with the **plasma membrane/cell cortex** via a **carboxy-terminal prenyl group**
|
|
GO:0005886
plasma membrane
|
TAS
Reactome:R-MMU-448947 |
ACCEPT |
Summary: plasma membrane is consistent with core Cdc42 GTPase, cytoskeletal, polarity, or localization biology.
Reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane localization, or immediate actin/polarity outputs.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
CDC42 associates with the **plasma membrane/cell cortex** via a **carboxy-terminal prenyl group**
|
|
GO:0005886
plasma membrane
|
TAS
Reactome:R-MMU-5665684 |
ACCEPT |
Summary: plasma membrane is consistent with core Cdc42 GTPase, cytoskeletal, polarity, or localization biology.
Reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane localization, or immediate actin/polarity outputs.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
CDC42 associates with the **plasma membrane/cell cortex** via a **carboxy-terminal prenyl group**
|
|
GO:0006897
endocytosis
|
IMP
PMID:24792215 CLN3 deficient cells display defects in the ARF1-Cdc42 pathw... |
KEEP AS NON CORE |
Summary: PMID:24792215 directly links Cdc42 cycling to actin-dependent fluid-phase endocytosis.
Reason: The process is supported for Cdc42-mediated actin cycling, but it remains a context-specific trafficking output rather than the core small-GTPase molecular function.
Supporting Evidence:
PMID:24792215
The small GTPase Cdc42 regulates sequential synthesis and break down of actin allowing fluid-phase uptake to occur
|
|
GO:0043209
myelin sheath
|
HDA
PMID:17634366 Proteolipid protein is required for transport of sirtuin 2 i... |
KEEP AS NON CORE |
Summary: myelin sheath is a supported context-specific Cdc42 output.
Reason: Cdc42 controls broad cellular architecture and developmental programs through actin, polarity, trafficking, and kinase-effector pathways, but this term is not the core molecular function.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
In its **GTP-bound state**, CDC42 binds effector proteins that drive downstream cytoskeletal and polarity responses
|
|
GO:0031256
leading edge membrane
|
IDA
PMID:22461490 DOCK8 is a Cdc42 activator critical for interstitial dendrit... |
ACCEPT |
Summary: leading edge membrane is consistent with core Cdc42 GTPase, cytoskeletal, polarity, or localization biology.
Reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane localization, or immediate actin/polarity outputs.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
CDC42 is directly linked to actin nucleation pathways through **WASP-family nucleation-promoting factors**.
|
|
GO:0036336
dendritic cell migration
|
IGI
PMID:22461490 DOCK8 is a Cdc42 activator critical for interstitial dendrit... |
KEEP AS NON CORE |
Summary: dendritic cell migration is a supported context-specific Cdc42 output.
Reason: Cdc42 controls broad cellular architecture and developmental programs through actin, polarity, trafficking, and kinase-effector pathways, but this term is not the core molecular function.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
In its **GTP-bound state**, CDC42 binds effector proteins that drive downstream cytoskeletal and polarity responses
|
|
GO:0005525
GTP binding
|
ISO
PMID:23620790 CBAP functions as a novel component in chemokine-induced ZAP... |
ACCEPT |
Summary: GTP binding is consistent with core Cdc42 GTPase, cytoskeletal, polarity, or localization biology.
Reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane localization, or immediate actin/polarity outputs.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
CDC42 is a **GTP-hydrolyzing enzyme** (small GTPase). Its substrate is **GTP**, which it binds and hydrolyzes to **GDP + Pi**
|
|
GO:0005911
cell-cell junction
|
IDA
PMID:23793062 The lymphoid lineage-specific actin-uncapping protein Rltpr ... |
KEEP AS NON CORE |
Summary: cell-cell junction is a supported context-specific Cdc42 output.
Reason: Cdc42 controls broad cellular architecture and developmental programs through actin, polarity, trafficking, and kinase-effector pathways, but this term is not the core molecular function.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
In its **GTP-bound state**, CDC42 binds effector proteins that drive downstream cytoskeletal and polarity responses
|
|
GO:0016020
membrane
|
ISS
GO_REF:0000024 |
ACCEPT |
Summary: membrane is consistent with core Cdc42 GTPase, cytoskeletal, polarity, or localization biology.
Reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane localization, or immediate actin/polarity outputs.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
CDC42 associates with the **plasma membrane/cell cortex** via a **carboxy-terminal prenyl group**
|
|
GO:1900026
positive regulation of substrate adhesion-dependent cell spreading
|
ISS
GO_REF:0000024 |
KEEP AS NON CORE |
Summary: positive regulation of substrate adhesion-dependent cell spreading is a supported context-specific Cdc42 output.
Reason: Cdc42 controls broad cellular architecture and developmental programs through actin, polarity, trafficking, and kinase-effector pathways, but this term is not the core molecular function.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
In its **GTP-bound state**, CDC42 binds effector proteins that drive downstream cytoskeletal and polarity responses
|
|
GO:0060501
positive regulation of epithelial cell proliferation involved in lung morphogenesis
|
IMP
PMID:23219958 CDC42 is required for structural patterning of the lung duri... |
KEEP AS NON CORE |
Summary: positive regulation of epithelial cell proliferation involved in lung morphogenesis is a supported context-specific Cdc42 output.
Reason: Cdc42 controls broad cellular architecture and developmental programs through actin, polarity, trafficking, and kinase-effector pathways, but this term is not the core molecular function.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
In its **GTP-bound state**, CDC42 binds effector proteins that drive downstream cytoskeletal and polarity responses
|
|
GO:0005515
protein binding
|
IPI
PMID:10954424 The mammalian homologue of the Caenorhabditis elegans polari... |
MARK AS OVER ANNOTATED |
Summary: protein binding records a physical association but is too generic to describe the gene product function.
Reason: The evidence supports regulated signaling-complex assembly, not a meaningful standalone protein binding function; more informative molecular and pathway terms capture the biology.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
In its **GTP-bound state**, CDC42 binds effector proteins that drive downstream cytoskeletal and polarity responses
|
|
GO:0005515
protein binding
|
IPI
PMID:11035016 A new family of Cdc42 effector proteins, CEPs, function in f... |
MARK AS OVER ANNOTATED |
Summary: protein binding records a physical association but is too generic to describe the gene product function.
Reason: The evidence supports regulated signaling-complex assembly, not a meaningful standalone protein binding function; more informative molecular and pathway terms capture the biology.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
In its **GTP-bound state**, CDC42 binds effector proteins that drive downstream cytoskeletal and polarity responses
|
|
GO:0003161
cardiac conduction system development
|
IGI
PMID:21690310 Tinman/Nkx2-5 acts via miR-1 and upstream of Cdc42 to regula... |
KEEP AS NON CORE |
Summary: cardiac conduction system development is a supported context-specific Cdc42 output.
Reason: Cdc42 controls broad cellular architecture and developmental programs through actin, polarity, trafficking, and kinase-effector pathways, but this term is not the core molecular function.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
In its **GTP-bound state**, CDC42 binds effector proteins that drive downstream cytoskeletal and polarity responses
|
|
GO:0060047
heart contraction
|
IGI
PMID:21690310 Tinman/Nkx2-5 acts via miR-1 and upstream of Cdc42 to regula... |
KEEP AS NON CORE |
Summary: heart contraction is a supported context-specific Cdc42 output.
Reason: Cdc42 controls broad cellular architecture and developmental programs through actin, polarity, trafficking, and kinase-effector pathways, but this term is not the core molecular function.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
In its **GTP-bound state**, CDC42 binds effector proteins that drive downstream cytoskeletal and polarity responses
|
|
GO:0019901
protein kinase binding
|
IPI
PMID:21048939 ARHGEF7 (Beta-PIX) acts as guanine nucleotide exchange facto... |
ACCEPT |
Summary: protein kinase binding is consistent with core Cdc42 GTPase, cytoskeletal, polarity, or localization biology.
Reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane localization, or immediate actin/polarity outputs.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
CDC42 is directly linked to actin nucleation pathways through **WASP-family nucleation-promoting factors**.
|
|
GO:0005515
protein binding
|
IPI
PMID:17000758 Ccpg1, a novel scaffold protein that regulates the activity ... |
MARK AS OVER ANNOTATED |
Summary: protein binding records a physical association but is too generic to describe the gene product function.
Reason: The evidence supports regulated signaling-complex assembly, not a meaningful standalone protein binding function; more informative molecular and pathway terms capture the biology.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
In its **GTP-bound state**, CDC42 binds effector proteins that drive downstream cytoskeletal and polarity responses
|
|
GO:0030496
midbody
|
ISS
GO_REF:0000024 |
ACCEPT |
Summary: midbody is consistent with core Cdc42 GTPase, cytoskeletal, polarity, or localization biology.
Reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane localization, or immediate actin/polarity outputs.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
CDC42 is directly linked to actin nucleation pathways through **WASP-family nucleation-promoting factors**.
|
|
GO:0032467
positive regulation of cytokinesis
|
ISS
GO_REF:0000024 |
ACCEPT |
Summary: positive regulation of cytokinesis is supported for Cdc42, but this is a cell-cycle output rather than the small GTPase catalytic role itself.
Reason: UniProt carries this transferred process annotation, but it is treated as a downstream cell-cycle output rather than core GTPase catalysis.
Supporting Evidence:
UniProt:P60766
GO; GO:0032467; P:positive regulation of cytokinesis; ISS:UniProtKB.
|
|
GO:0051233
spindle midzone
|
ISS
GO_REF:0000024 |
ACCEPT |
Summary: spindle midzone is consistent with core Cdc42 GTPase, cytoskeletal, polarity, or localization biology.
Reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane localization, or immediate actin/polarity outputs.
Supporting Evidence:
UniProt:P60766
Moves to the central spindle as cells progressed through anaphase to telophase.
|
|
GO:0051489
regulation of filopodium assembly
|
ISS
GO_REF:0000024 |
ACCEPT |
Summary: regulation of filopodium assembly is consistent with core Cdc42 GTPase, cytoskeletal, polarity, or localization biology.
Reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane localization, or immediate actin/polarity outputs.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
CDC42 is directly linked to actin nucleation pathways through **WASP-family nucleation-promoting factors**.
|
|
GO:0051988
regulation of attachment of spindle microtubules to kinetochore
|
ISS
GO_REF:0000024 |
ACCEPT |
Summary: regulation of attachment of spindle microtubules to kinetochore is consistent with core Cdc42 GTPase, cytoskeletal, polarity, or localization biology.
Reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane localization, or immediate actin/polarity outputs.
Supporting Evidence:
UniProt:P60766
Regulates the bipolar attachment of spindle microtubules to kinetochores before chromosome congression in metaphase.
|
|
GO:0072686
mitotic spindle
|
ISS
GO_REF:0000024 |
ACCEPT |
Summary: mitotic spindle is consistent with core Cdc42 GTPase, cytoskeletal, polarity, or localization biology.
Reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane localization, or immediate actin/polarity outputs.
Supporting Evidence:
UniProt:P60766
Cytoplasm, cytoskeleton, spindle
|
|
GO:0005737
cytoplasm
|
IDA
PMID:19796622 Uncovering early response of gene regulatory networks in ESC... |
ACCEPT |
Summary: cytoplasm is consistent with core Cdc42 GTPase, cytoskeletal, polarity, or localization biology.
Reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane localization, or immediate actin/polarity outputs.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
CDC42 associates with the **plasma membrane/cell cortex** via a **carboxy-terminal prenyl group**
|
|
GO:0071944
cell periphery
|
IDA
PMID:19796622 Uncovering early response of gene regulatory networks in ESC... |
ACCEPT |
Summary: cell periphery is consistent with core Cdc42 GTPase, cytoskeletal, polarity, or localization biology.
Reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane localization, or immediate actin/polarity outputs.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
CDC42 associates with the **plasma membrane/cell cortex** via a **carboxy-terminal prenyl group**
|
|
GO:0005737
cytoplasm
|
IDA
PMID:15775979 E-cadherin is essential for in vivo epidermal barrier functi... |
ACCEPT |
Summary: cytoplasm is consistent with core Cdc42 GTPase, cytoskeletal, polarity, or localization biology.
Reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane localization, or immediate actin/polarity outputs.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
CDC42 associates with the **plasma membrane/cell cortex** via a **carboxy-terminal prenyl group**
|
|
GO:0043410
positive regulation of MAPK cascade
|
IDA
PMID:19244314 Cdo promotes neuronal differentiation via activation of the ... |
KEEP AS NON CORE |
Summary: positive regulation of MAPK cascade is supported in a Cdo/JLP/Bnip-2 neuronal differentiation context, but it is not Cdc42's core molecular role.
Reason: The cited evidence supports a context-specific Cdc42/p38 MAPK signaling output.
Supporting Evidence:
PMID:19244314
These molecules regulate Cdc42 and p38MAPK activities, which increase in a Cdo-dependent manner during neuronal differentiation of C17.2 cells and retinoic acid-treated P19 cells.
|
|
GO:0003924
GTPase activity
|
ISA
PMID:12637522 Multifunctional roles for the PH domain of Dbs in regulating... |
ACCEPT |
Summary: GTPase activity is consistent with core Cdc42 GTPase, cytoskeletal, polarity, or localization biology.
Reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane localization, or immediate actin/polarity outputs.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
CDC42 is a **GTP-hydrolyzing enzyme** (small GTPase). Its substrate is **GTP**, which it binds and hydrolyzes to **GDP + Pi**
|
|
GO:0007097
nuclear migration
|
IMP
PMID:16892058 The Rho-GTPase cdc42 regulates neural progenitor fate at the... |
KEEP AS NON CORE |
Summary: nuclear migration is a supported context-specific Cdc42 output.
Reason: Cdc42 controls broad cellular architecture and developmental programs through actin, polarity, trafficking, and kinase-effector pathways, but this term is not the core molecular function.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
In its **GTP-bound state**, CDC42 binds effector proteins that drive downstream cytoskeletal and polarity responses
|
|
GO:0008104
intracellular protein localization
|
IMP
PMID:16621792 Membrane localization of adenomatous polyposis coli protein ... |
KEEP AS NON CORE |
Summary: intracellular protein localization is a supported context-specific Cdc42 output.
Reason: Cdc42 controls broad cellular architecture and developmental programs through actin, polarity, trafficking, and kinase-effector pathways, but this term is not the core molecular function.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
In its **GTP-bound state**, CDC42 binds effector proteins that drive downstream cytoskeletal and polarity responses
|
|
GO:0034332
adherens junction organization
|
IMP
PMID:16892058 The Rho-GTPase cdc42 regulates neural progenitor fate at the... |
KEEP AS NON CORE |
Summary: adherens junction organization is a supported context-specific Cdc42 output.
Reason: Cdc42 controls broad cellular architecture and developmental programs through actin, polarity, trafficking, and kinase-effector pathways, but this term is not the core molecular function.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
In its **GTP-bound state**, CDC42 binds effector proteins that drive downstream cytoskeletal and polarity responses
|
|
GO:0035088
establishment or maintenance of apical/basal cell polarity
|
IMP
PMID:16892058 The Rho-GTPase cdc42 regulates neural progenitor fate at the... |
ACCEPT |
Summary: establishment or maintenance of apical/basal cell polarity is consistent with core Cdc42 GTPase, cytoskeletal, polarity, or localization biology.
Reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane localization, or immediate actin/polarity outputs.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
CDC42 is directly linked to actin nucleation pathways through **WASP-family nucleation-promoting factors**.
|
|
GO:0051647
nucleus localization
|
IMP
PMID:16892058 The Rho-GTPase cdc42 regulates neural progenitor fate at the... |
KEEP AS NON CORE |
Summary: nucleus localization is a supported context-specific Cdc42 output.
Reason: Cdc42 controls broad cellular architecture and developmental programs through actin, polarity, trafficking, and kinase-effector pathways, but this term is not the core molecular function.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
In its **GTP-bound state**, CDC42 binds effector proteins that drive downstream cytoskeletal and polarity responses
|
|
GO:0007088
regulation of mitotic nuclear division
|
IMP
PMID:16892058 The Rho-GTPase cdc42 regulates neural progenitor fate at the... |
KEEP AS NON CORE |
Summary: regulation of mitotic nuclear division is a supported context-specific Cdc42 output.
Reason: Cdc42 controls broad cellular architecture and developmental programs through actin, polarity, trafficking, and kinase-effector pathways, but this term is not the core molecular function.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
In its **GTP-bound state**, CDC42 binds effector proteins that drive downstream cytoskeletal and polarity responses
|
|
GO:0045177
apical part of cell
|
IDA
PMID:16892058 The Rho-GTPase cdc42 regulates neural progenitor fate at the... |
KEEP AS NON CORE |
Summary: apical part of cell is a supported context-specific Cdc42 output.
Reason: Cdc42 controls broad cellular architecture and developmental programs through actin, polarity, trafficking, and kinase-effector pathways, but this term is not the core molecular function.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
In its **GTP-bound state**, CDC42 binds effector proteins that drive downstream cytoskeletal and polarity responses
|
|
GO:0048664
neuron fate determination
|
IMP
PMID:16892058 The Rho-GTPase cdc42 regulates neural progenitor fate at the... |
KEEP AS NON CORE |
Summary: neuron fate determination is a supported context-specific Cdc42 output.
Reason: Cdc42 controls broad cellular architecture and developmental programs through actin, polarity, trafficking, and kinase-effector pathways, but this term is not the core molecular function.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
In its **GTP-bound state**, CDC42 binds effector proteins that drive downstream cytoskeletal and polarity responses
|
|
GO:0007163
establishment or maintenance of cell polarity
|
TAS
PMID:10954424 The mammalian homologue of the Caenorhabditis elegans polari... |
ACCEPT |
Summary: establishment or maintenance of cell polarity is consistent with core Cdc42 GTPase, cytoskeletal, polarity, or localization biology.
Reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane localization, or immediate actin/polarity outputs.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
CDC42 is directly linked to actin nucleation pathways through **WASP-family nucleation-promoting factors**.
|
|
GO:0016197
endosomal transport
|
TAS
PMID:10954424 The mammalian homologue of the Caenorhabditis elegans polari... |
KEEP AS NON CORE |
Summary: endosomal transport is a supported context-specific Cdc42 output.
Reason: Cdc42 controls broad cellular architecture and developmental programs through actin, polarity, trafficking, and kinase-effector pathways, but this term is not the core molecular function.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
In its **GTP-bound state**, CDC42 binds effector proteins that drive downstream cytoskeletal and polarity responses
|
|
GO:0098609
cell-cell adhesion
|
TAS
PMID:10954424 The mammalian homologue of the Caenorhabditis elegans polari... |
KEEP AS NON CORE |
Summary: cell-cell adhesion is a supported context-specific Cdc42 output.
Reason: Cdc42 controls broad cellular architecture and developmental programs through actin, polarity, trafficking, and kinase-effector pathways, but this term is not the core molecular function.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
In its **GTP-bound state**, CDC42 binds effector proteins that drive downstream cytoskeletal and polarity responses
|
|
GO:0007097
nuclear migration
|
IMP
PMID:15882626 Nuclear movement regulated by Cdc42, MRCK, myosin, and actin... |
KEEP AS NON CORE |
Summary: nuclear migration is a supported context-specific Cdc42 output.
Reason: Cdc42 controls broad cellular architecture and developmental programs through actin, polarity, trafficking, and kinase-effector pathways, but this term is not the core molecular function.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
In its **GTP-bound state**, CDC42 binds effector proteins that drive downstream cytoskeletal and polarity responses
|
|
GO:0005515
protein binding
|
IPI
PMID:15996550 The Rho-specific GEF Lfc interacts with neurabin and spinoph... |
MARK AS OVER ANNOTATED |
Summary: protein binding records a physical association but is too generic to describe the gene product function.
Reason: The evidence supports regulated signaling-complex assembly, not a meaningful standalone protein binding function; more informative molecular and pathway terms capture the biology.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
In its **GTP-bound state**, CDC42 binds effector proteins that drive downstream cytoskeletal and polarity responses
|
|
GO:0042995
cell projection
|
IDA
PMID:15728722 Local phosphatidylinositol 3,4,5-trisphosphate accumulation ... |
KEEP AS NON CORE |
Summary: cell projection is a supported context-specific Cdc42 output.
Reason: Cdc42 controls broad cellular architecture and developmental programs through actin, polarity, trafficking, and kinase-effector pathways, but this term is not the core molecular function.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
In its **GTP-bound state**, CDC42 binds effector proteins that drive downstream cytoskeletal and polarity responses
|
|
GO:0051897
positive regulation of phosphatidylinositol 3-kinase/protein kinase B signal transduction
|
IMP
PMID:15728722 Local phosphatidylinositol 3,4,5-trisphosphate accumulation ... |
KEEP AS NON CORE |
Summary: positive regulation of phosphatidylinositol 3-kinase/protein kinase B signal transduction is a supported context-specific Cdc42 output.
Reason: Cdc42 controls broad cellular architecture and developmental programs through actin, polarity, trafficking, and kinase-effector pathways, but this term is not the core molecular function.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
In its **GTP-bound state**, CDC42 binds effector proteins that drive downstream cytoskeletal and polarity responses
|
|
GO:0005515
protein binding
|
IPI
PMID:16052498 Expression, synaptic localization, and developmental regulat... |
MARK AS OVER ANNOTATED |
Summary: protein binding records a physical association but is too generic to describe the gene product function.
Reason: The evidence supports regulated signaling-complex assembly, not a meaningful standalone protein binding function; more informative molecular and pathway terms capture the biology.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
In its **GTP-bound state**, CDC42 binds effector proteins that drive downstream cytoskeletal and polarity responses
|
|
GO:0005515
protein binding
|
IPI
PMID:12773384 TCGAP, a multidomain Rho GTPase-activating protein involved ... |
MARK AS OVER ANNOTATED |
Summary: protein binding records a physical association but is too generic to describe the gene product function.
Reason: The evidence supports regulated signaling-complex assembly, not a meaningful standalone protein binding function; more informative molecular and pathway terms capture the biology.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
In its **GTP-bound state**, CDC42 binds effector proteins that drive downstream cytoskeletal and polarity responses
|
|
GO:0003924
GTPase activity
|
IDA
PMID:15249579 Vav GEFs are required for beta2 integrin-dependent functions... |
ACCEPT |
Summary: GTPase activity is consistent with core Cdc42 GTPase, cytoskeletal, polarity, or localization biology.
Reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane localization, or immediate actin/polarity outputs.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
CDC42 is a **GTP-hydrolyzing enzyme** (small GTPase). Its substrate is **GTP**, which it binds and hydrolyzes to **GDP + Pi**
|
|
GO:0030742
GTP-dependent protein binding
|
IPI
PMID:10954424 The mammalian homologue of the Caenorhabditis elegans polari... |
ACCEPT |
Summary: GTP-dependent protein binding is consistent with core Cdc42 GTPase, cytoskeletal, polarity, or localization biology.
Reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane localization, or immediate actin/polarity outputs.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
CDC42 is directly linked to actin nucleation pathways through **WASP-family nucleation-promoting factors**.
|
|
GO:0003924
GTPase activity
|
IDA
PMID:10699171 Functional analysis of ARHGAP6, a novel GTPase-activating pr... |
ACCEPT |
Summary: GTPase activity is consistent with core Cdc42 GTPase, cytoskeletal, polarity, or localization biology.
Reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane localization, or immediate actin/polarity outputs.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
CDC42 is a **GTP-hydrolyzing enzyme** (small GTPase). Its substrate is **GTP**, which it binds and hydrolyzes to **GDP + Pi**
|
|
GO:0046847
filopodium assembly
|
IDA
PMID:10699171 Functional analysis of ARHGAP6, a novel GTPase-activating pr... |
ACCEPT |
Summary: filopodium assembly is consistent with core Cdc42 GTPase, cytoskeletal, polarity, or localization biology.
Reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane localization, or immediate actin/polarity outputs.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
CDC42 is directly linked to actin nucleation pathways through **WASP-family nucleation-promoting factors**.
|
|
GO:0003924
GTPase activity
|
TAS
PMID:10490598 The Borgs, a new family of Cdc42 and TC10 GTPase-interacting... |
ACCEPT |
Summary: GTPase activity is consistent with core Cdc42 GTPase, cytoskeletal, polarity, or localization biology.
Reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane localization, or immediate actin/polarity outputs.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
CDC42 is a **GTP-hydrolyzing enzyme** (small GTPase). Its substrate is **GTP**, which it binds and hydrolyzes to **GDP + Pi**
|
|
GO:0007266
Rho protein signal transduction
|
TAS
PMID:10490598 The Borgs, a new family of Cdc42 and TC10 GTPase-interacting... |
ACCEPT |
Summary: Rho protein signal transduction is consistent with core Cdc42 GTPase, cytoskeletal, polarity, or localization biology.
Reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane localization, or immediate actin/polarity outputs.
Supporting Evidence:
file:mouse/Cdc42/Cdc42-deep-research-falcon.md
CDC42 is directly linked to actin nucleation pathways through **WASP-family nucleation-promoting factors**.
|
Q: Which mouse Cdc42 annotations should be isoform-qualified for prenylated versus palmitoylated Cdc42 products?
Q: Which neuronal/synaptic Cdc42 terms are directly supported for the brain-enriched isoform rather than inferred from general Rho-family biology?
Experiment: Use isoform-specific knock-in tags and rescue alleles to measure Cdc42 effector recruitment at leading edge, Golgi/endosomal, midbody, and neuronal compartments.
Hypothesis: Cdc42 pleiotropy is primarily explained by isoform- and lipidation-dependent localization rather than different intrinsic GTPase biochemistry.
Type: Live-cell imaging and isoform-specific rescue
provider: falcon
model: Edison Scientific Literature
cached: false
start_time: '2026-05-03T13:35:53.237513'
end_time: '2026-05-03T13:50:38.849863'
duration_seconds: 885.61
template_file: templates/gene_research_go_focused.md
template_variables:
organism: mouse
gene_id: Cdc42
gene_symbol: Cdc42
uniprot_accession: P60766
protein_description: 'RecName: Full=Cell division control protein 42 homolog {ECO:0000305};
EC=3.6.5.2 {ECO:0000269|PubMed:24352656, ECO:0000269|PubMed:26969129}; AltName:
Full=G25K GTP-binding protein; Flags: Precursor;'
gene_info: Name=Cdc42 {ECO:0000312|MGI:MGI:106211};
organism_full: Mus musculus (Mouse).
protein_family: Belongs to the small GTPase superfamily. Rho family. CDC42
protein_domains: Cdc42. (IPR037874); P-loop_NTPase. (IPR027417); Small_GTP-bd. (IPR005225);
Small_GTPase. (IPR001806); Small_GTPase_Rho. (IPR003578)
provider_config:
timeout: 600
max_retries: 3
parameters:
allowed_domains: []
temperature: 0.1
citation_count: 42
BEFORE YOU BEGIN RESEARCH: You MUST verify you are researching the CORRECT gene/protein. Gene symbols can be ambiguous, especially for less well-characterized genes from non-model organisms.
DO NOT PROCEED WITH RESEARCH ON A DIFFERENT GENE. Instead:
- State clearly: "The gene symbol 'Cdc42' is ambiguous or literature is limited for this specific protein"
- Explain what you found (e.g., "Found extensive literature on a different gene with the same symbol in a different organism")
- Describe the protein based ONLY on the UniProt information provided above
- Suggest that the protein function can be inferred from domain/family information
Please provide a comprehensive research report on the gene Cdc42 (gene ID: Cdc42, UniProt: P60766) in mouse.
The research report should be a detailed narrative explaining the function, biological processes, and localization of the gene product. Citations should be given for all claims.
You should prioritize authoritative reviews and primary scientific literature when conducting research. You can supplement
this with annotations you find in gene/protein databases, but these can be outdated or inaccurate.
We are specifically interested in the primary function of the gene - for enzymes, what reaction is catalyzed, and what is the substrate specificity? For transporters, what is the substrate? For structural proteins or adapters, what is the broader structural role? For signaling molecules, what is the role in the pathway.
We are interested in where in or outside the cell the gene product carries out its function.
We are also interested in the signaling or biochemical pathways in which the gene functions. We are less interested in broad pleiotropic effects, except where these elucidate the precise role.
Include evidence where possible. We are interested in both experimental evidence as well as inference from structure, evolution, or bioinformatic analysis. Precise studies should be prioritized over high-throughput, where available.
Question: You are an expert researcher providing comprehensive, well-cited information.
Provide detailed information focusing on:
1. Key concepts and definitions with current understanding
2. Recent developments and latest research (prioritize 2023-2024 sources)
3. Current applications and real-world implementations
4. Expert opinions and analysis from authoritative sources
5. Relevant statistics and data from recent studies
Format as a comprehensive research report with proper citations. Include URLs and publication dates where available.
Always prioritize recent, authoritative sources and provide specific citations for all major claims.
BEFORE YOU BEGIN RESEARCH: You MUST verify you are researching the CORRECT gene/protein. Gene symbols can be ambiguous, especially for less well-characterized genes from non-model organisms.
DO NOT PROCEED WITH RESEARCH ON A DIFFERENT GENE. Instead:
- State clearly: "The gene symbol 'Cdc42' is ambiguous or literature is limited for this specific protein"
- Explain what you found (e.g., "Found extensive literature on a different gene with the same symbol in a different organism")
- Describe the protein based ONLY on the UniProt information provided above
- Suggest that the protein function can be inferred from domain/family information
Please provide a comprehensive research report on the gene Cdc42 (gene ID: Cdc42, UniProt: P60766) in mouse.
The research report should be a detailed narrative explaining the function, biological processes, and localization of the gene product. Citations should be given for all claims.
You should prioritize authoritative reviews and primary scientific literature when conducting research. You can supplement
this with annotations you find in gene/protein databases, but these can be outdated or inaccurate.
We are specifically interested in the primary function of the gene - for enzymes, what reaction is catalyzed, and what is the substrate specificity? For transporters, what is the substrate? For structural proteins or adapters, what is the broader structural role? For signaling molecules, what is the role in the pathway.
We are interested in where in or outside the cell the gene product carries out its function.
We are also interested in the signaling or biochemical pathways in which the gene functions. We are less interested in broad pleiotropic effects, except where these elucidate the precise role.
Include evidence where possible. We are interested in both experimental evidence as well as inference from structure, evolution, or bioinformatic analysis. Precise studies should be prioritized over high-throughput, where available.
The requested target is mouse (Mus musculus) Cdc42, UniProt P60766, described as “cell division control protein 42 homolog,” a classical Rho-family small GTPase. In the retrieved literature corpus, the protein is consistently described as Cdc42/CDC42, a Rho-family small GTPase acting as a GDP/GTP-regulated molecular switch, regulated by GEFs, GAPs, and GDIs (dai2023theroleof pages 1-2, yin2023targetingsmallgtpases pages 1-2). Several sources explicitly discuss two CDC42 protein isoforms distinguished by their C-termini (prenylated vs palmitoylated), matching the UniProt family/domain expectations for Cdc42 (small GTPase, P-loop NTPase) and supporting that we are researching the correct gene/protein family context (ravichandran2024thedistinctlocalization pages 1-2, wirth2023lipidationofsmall pages 2-4).
Important limitation: within the retrieved full texts, the literal UniProt accession “P60766” was not found in an evidence passage; thus, accession-level confirmation relies on the user-provided UniProt identity rather than being re-quoted from a paper in this tool run.
CDC42 belongs to the Rho family of small GTPases and acts as a molecular switch cycling between GTP-bound (active) and GDP-bound (inactive) states (dai2023theroleof pages 1-2, yin2023targetingsmallgtpases pages 1-2). In its GTP-bound state, CDC42 binds effector proteins that drive downstream cytoskeletal and polarity responses, while the GDP-bound state is generally inactive (bement2024patterningofthe pages 1-6).
The canonical regulatory framework is:
- GEFs accelerate GDP release / GTP loading (activation) (bement2024patterningofthe pages 1-6, dai2023theroleof pages 1-2).
- GAPs stimulate GTP hydrolysis (inactivation), important because intrinsic hydrolysis is slow (bement2024patterningofthe pages 1-6, bement2024patterningofthe pages 6-8).
- RhoGDIs bind lipidated Rho GTPases, shielding the prenyl group and maintaining a soluble cytosolic pool; they can also extract inactive GTPases from membranes, thereby limiting access to GEFs (bement2024patterningofthe pages 1-6, hawkins2023theautoinflammatoryc188y pages 36-40).
A major modern view is that Rho-family GTPases (including CDC42) can generate self-organized cortical patterns (patches/stripes/rings/waves). A 2024 authoritative review emphasizes that Rho GTPases have very low intrinsic hydrolysis and short plasma-membrane residence times (seconds or less), so continuous cycling coordinated by localized GEF and GAP activities is required for stable spatial patterns (“GTPase flux” concepts) (bement2024patterningofthe pages 6-8, bement2024patterningofthe pages 1-6).
CDC42 is a GTP-hydrolyzing enzyme (small GTPase). Its substrate is GTP, which it binds and hydrolyzes to GDP + Pi, with the rate strongly accelerated by GAPs in vivo (bement2024patterningofthe pages 1-6, dai2023theroleof pages 1-2). This biochemical activity is coupled to conformational switching that enables selective binding to downstream effectors when GTP-bound (bement2024patterningofthe pages 1-6).
CDC42 associates with the plasma membrane/cell cortex via a carboxy-terminal prenyl group, which enables access to cortical effectors controlling actin and myosin organization (bement2024patterningofthe pages 1-6). The prenyl group can be shielded by RhoGDI, supporting a cytosolic pool and enabling extraction from membranes (bement2024patterningofthe pages 1-6).
Recent work emphasizes that mammalian CDC42 exists as two isoforms distinguished by the short C-terminal sequence and lipidation:
- A prenylated isoform with a canonical CaaX motif ending in CVLL (Cdc42-prenyl), broadly expressed across tissues (wirth2023lipidationofsmall pages 2-4).
- A brain-enriched palmitoylatable isoform with a non-canonical CCaX motif ending in CCIF (Cdc42-palm), which can be palmitoylated and shows brain-enriched localization patterns (e.g., dendritic compartments/spines) (wirth2023lipidationofsmall pages 2-4).
A mechanistic study showed that the CCaX isoform can undergo dual lipidation (prenylation + palmitoylation) and that palmitoylation state impacts interaction with RhoGDI (nishimura2013identificationofa pages 1-3, nishimura2013identificationofa pages 6-7).
A 2024 Journal of Cell Biology study provides a clear functional model:
- CDC42u (ubiquitous/prenylated) localizes to the leading-edge plasma membrane during migration and recruits polarity machinery.
- CDC42b (brain/palmitoylated) localizes primarily to intracellular membrane compartments and supports specific endocytic programs.
These distinctions arise from C-terminal lipidation rules and CAAX-dependent targeting (ravichandran2024thedistinctlocalization pages 1-2).
The associated figures (isoform sequences, localization, and polarity-complex recruitment) are shown in the paper’s early figures (ravichandran2024thedistinctlocalization media a8180683, ravichandran2024thedistinctlocalization media 96b45e8a, ravichandran2024thedistinctlocalization media dd806cca, ravichandran2024thedistinctlocalization media 8ba5d15d, ravichandran2024thedistinctlocalization media 890df85d).
Isoform-resolved work indicates CDC42u is a key activator/recruiter of the Par6–PKCζ/aPKC polarity axis at the leading edge in migrating cells (ravichandran2024thedistinctlocalization pages 1-2, ravichandran2023thefunctionalspecificity pages 4-7). In tissue contexts, reduced Cdc42/Cdc42-GTP correlates with impaired assembly of polarity complexes involving Par6/Par3/αPKC in liver cells (cholangiocytes and hepatocytes) (ravichandran2024thedistinctlocalization media a8180683).
CDC42 is directly linked to actin nucleation pathways through WASP-family nucleation-promoting factors. In primary T cell work, CDC42 is explicitly stated to activate WASP, consistent with a role in Arp2/3-mediated actin assembly (rochussen2025transcriptionaladaptationafter pages 33-34). Isoform-resolved cell migration/endocytosis studies further connect CDC42b to N-WASP–mediated endocytosis/macropinocytosis programs, with N-WASP perturbation phenocopying CDC42b loss in uptake assays (ravichandran2024thedistinctlocalization pages 1-2, ravichandran2023thefunctionalspecificity pages 7-9).
CDC42 signaling commonly propagates via p21-activated kinases (PAKs). In a 2024 mouse Alzheimer’s disease model study, Rac1/Cdc42 pathway activity is profiled using phosphorylation markers pRac/Cdc42 (Ser71; inactive marker) and pPAK (Thr423; active PAK marker) (akhtar2024spatialandplanar pages 1-3). A mechanistic narrative of CDC42 effector binding includes PAK kinases among key effectors (hawkins2023theautoinflammatoryc188y pages 36-40).
CDC42 localizes and functions at membrane trafficking hubs. A mouse intestinal organoid study (preprint) linked polarized trafficking defects to mis-targeting of Rab11+ apical recycling endosomes and of the polarity determinant Cdc42, with downstream engagement of YAP and EGFR/mTOR-associated proliferation pathways (ravichandran2023thefunctionalspecificity pages 4-7).
A major 2024 advance is mechanistic separation of CDC42 isoform functions by localization:
- CDC42u supports front-rear polarity via the Par6–PKCζ pathway at the leading edge.
- CDC42b supports N-WASP–mediated endocytosis from intracellular compartments.
Quantitatively, combined knockdown of both isoforms reduced directionality (~83% → ~55%) and persistence (~85% → ~60%) in migrating cells, with CDC42u depletion driving much of this phenotype (ravichandran2024thedistinctlocalization pages 1-2).
In 3xTg-AD mice, a 2024 study reported decreased cortical pRac/Cdc42 with increased pPAK, plus spatial gradients (rostral vs caudal) and plane-specific nuclear/cytoplasmic redistribution patterns (akhtar2024spatialandplanar pages 1-3). This supports the view that Rac1/Cdc42 signaling can be regionally reconfigured in neurodegenerative disease contexts.
A high-impact 2024 Nature Reviews Molecular Cell Biology article reframed Rho GTPases (including CDC42) as excitable/self-organizing systems where spatial patterns rely on rapid cycling and coupled GEF/GAP activities, with relevant quantitative scales (seconds-to-minutes patterns; membrane half-lives of seconds) (bement2024patterningofthe pages 6-8, bement2024patterningofthe pages 1-6).
A 2023 review focused specifically on CDC42 lipidation describes how prenylation/palmitoylation and sequence features (e.g., polybasic motifs) dictate microdomain and compartment targeting, including the distinction between CVLL prenylated and CCIF palmitoylatable isoforms, and relates these targeting rules to developmental polarity phenotypes (wirth2023lipidationofsmall pages 2-4).
In practice, CDC42 is implemented primarily through mouse conditional genetics and ex vivo organoid/primary cell models to dissect polarity, trafficking, immunity, and regeneration:
- Mouse disease-model profiling of Rac1/Cdc42-PAK signaling in brain tissue (akhtar2024spatialandplanar pages 1-3).
- Mouse intestinal organoids linking epithelial trafficking/polarity to Cdc42 localization (ravichandran2023thefunctionalspecificity pages 4-7).
- Conditional knockout-based studies of stem/progenitor cell polarity maintenance via CDC42 translation control (rochussen2025transcriptionaladaptationafter pages 3-6).
A 2023 review on small-GTPase targeting emphasizes that many small GTPases remain challenging to drug directly, but the field is developing strategies (e.g., inhibitor modalities and targeting regulatory mechanisms) and positions Rho-family proteins (including CDC42) as disease-relevant targets (yin2023targetingsmallgtpases pages 1-2).
Expert synthesis from 2024 emphasizes that CDC42’s functional outputs are inseparable from where and how long it is active at membranes: rapid membrane residence, GDI-mediated extraction, and continuous flux through GEF/GAP cycles enable spatially patterned signaling at the cortex (bement2024patterningofthe pages 6-8, bement2024patterningofthe pages 1-6).
The 2024 isoform study supports a strong interpretive point: CDC42 isoforms appear to have similar biochemical binding capabilities, but distinct localization routes signaling to different modules (polarity at leading edge vs endocytosis from internal membranes) (ravichandran2024thedistinctlocalization pages 1-2). This provides a mechanistic framework for reconciling CDC42’s broad pleiotropy with pathway specificity.
The following table compiles the main functional-annotation points (identity → molecular function → localization → pathways → quantitative results → applications) with publication dates and URLs.
| Topic | Key points | Evidence/Study (first author year) | Publication date | URL | Notes (mouse-specific vs general) |
|---|---|---|---|---|---|
| identity | UniProt P60766 corresponds to mouse Cdc42, a classical Rho-family small GTPase that functions as a molecular switch cycling between GTP-bound active and GDP-bound inactive states; activity is controlled by GEFs, GAPs, and GDIs. (dai2023theroleof pages 1-2, yin2023targetingsmallgtpases pages 1-2) | Dai 2023; Yin 2023 | 2023-03; 2023-05 | https://doi.org/10.4103/1673-5374.369101; https://doi.org/10.1038/s41392-023-01441-4 | General Rho/CDC42 biology; applicable to mouse CDC42 |
| function | Primary biochemical function is GTP binding and hydrolysis to regulate cortical actin/myosin responses; intrinsic GTP hydrolysis is slow and is accelerated by GAPs, while GEFs accelerate nucleotide exchange. Inactive CDC42 can be extracted from membranes by RhoGDI. (bement2024patterningofthe pages 1-6, bement2024patterningofthe pages 6-8) | Bement 2024 | 2024-01 | https://doi.org/10.1038/s41580-023-00682-z | General mechanistic review, not mouse-sequence-specific |
| localization | Active CDC42 associates with the plasma membrane via carboxy-terminal prenylation; RhoGDI shields the prenyl group to maintain a soluble cytosolic pool. Cortical CDC42 activity forms dynamic zones with lifetimes of seconds to minutes. (bement2024patterningofthe pages 1-6, bement2024patterningofthe pages 6-8) | Bement 2024 | 2024-01 | https://doi.org/10.1038/s41580-023-00682-z | General Rho-family mechanism relevant to mouse CDC42 |
| localization | CDC42 membrane targeting depends on C-terminal lipidation. The prenylated isoform carries a CaaX motif ending CVLL; a brain-enriched isoform carries CCIF and can be palmitoylated. Prenylated CDC42 is broadly expressed, whereas palmitoylated CDC42 is enriched in brain and associates with dendritic compartments/spines. (wirth2023lipidationofsmall pages 2-4, nishimura2013identificationofa pages 1-3) | Wirth 2023; Nishimura 2013 | 2023-01; 2013-04 | https://doi.org/10.3389/fphys.2022.1088840; https://doi.org/10.1128/mcb.01398-12 | Mix of general and isoform-specific evidence; includes mammalian/neuronal systems |
| localization | Isoform-specific localization helps explain function: CDC42u localizes mainly to leading-edge plasma membrane/cytosol, whereas CDC42b localizes mainly to intracellular membranes including Golgi and early endosomes; both can accumulate at the leading edge. (ravichandran2024thedistinctlocalization pages 1-2, ravichandran2023thefunctionalspecificity pages 7-9) | Ravichandran 2024; Ravichandran 2023 | 2024-02; 2023-05 | https://doi.org/10.1083/jcb.202004092; https://doi.org/10.1101/2023.02.27.528078 | Mammalian primary cells; mechanism general to CDC42 isoforms |
| pathways | Key downstream effectors include PAK and WASP/N-WASP family proteins; CDC42 also regulates Par6–PKCζ/aPKC polarity signaling and actin nucleation/filopodia-related pathways. (rochussen2025transcriptionaladaptationafter pages 33-34, ravichandran2024thedistinctlocalization pages 1-2, hawkins2023theautoinflammatoryc188y pages 36-40) | Rochussen 2025; Ravichandran 2024; Hawkins 2023 | 2025-07; 2024-02; 2023 | https://doi.org/10.1242/jcs.263826; https://doi.org/10.1083/jcb.202004092; https://doi.org/10.1083/jcb.202004092 | Mixed evidence; PAK/WASP are general CDC42 effectors, Par6 pathway supported in mammalian cells |
| pathways | In mouse liver, reduced Cdc42/Cdc42-GTP disrupts polarity complexes and junctional organization; Cdc42 acts with Par6/Par3/αPKC to assemble polarity complexes in cholangiocytes/hepatocytes. (ravichandran2024thedistinctlocalization media a8180683) | Zhou 2021 | 2021-05 | https://doi.org/10.7150/thno.49116 | Mouse-specific in vivo evidence |
| pathways | In mouse/intestinal systems, CDC42 supports epithelial polarity and trafficking; AP-1B loss mislocalizes Cdc42 in mouse intestinal organoids, linking polarized trafficking defects to YAP and EGFR/mTOR-associated proliferative responses. (ravichandran2023thefunctionalspecificity pages 4-7) | Duclos 2023 | 2023-05 | https://doi.org/10.1101/2023.05.12.540539 | Mouse organoid/preprint evidence |
| function | In hematopoietic stem/progenitor cells, CDC42 is required for polarity and asymmetric segregation; SYNCRIP loss reduces CDC42 translation and forced CDC42 expression rescues polarity and in vitro replating activity. (rochussen2025transcriptionaladaptationafter pages 3-6) | Chavez 2023 | 2023-04 | https://doi.org/10.1038/s41467-023-38001-x | Mouse conditional-knockout-based evidence |
| quant data | Dynamic cortical CDC42 zones can appear/disappear within seconds to minutes; membrane half-lives of Rho GTPases are several seconds or less, supporting rapid turnover models. (bement2024patterningofthe pages 6-8) | Bement 2024 | 2024-01 | https://doi.org/10.1038/s41580-023-00682-z | General quantitative cell-biophysics data |
| quant data | In 3xTg-AD mouse brain, cortical pRac/Cdc42 is decreased while pPAK is increased; serial-section profiling showed rostral increase and caudal decrease of pRac/Cdc42 plus plane-specific nuclear-to-cytoplasmic redistribution. (akhtar2024spatialandplanar pages 1-3) | Akhtar 2024 | 2024-11 | https://doi.org/10.1177/13872877241291076 | Mouse-specific disease-model evidence |
| quant data | In migrating mammalian cells, depletion of both CDC42 isoforms reduced migration directionality from ~83% to ~55% and persistence from ~85% to ~60%; CDC42u depletion produced similar defects. (ravichandran2024thedistinctlocalization pages 1-2) | Ravichandran 2024 | 2024-02 | https://doi.org/10.1083/jcb.202004092 | Mammalian cell-based quantitative evidence |
| quant data | In neural precursor/macropinocytosis assays, double CDC42 isoform knockdown reduced dextran uptake by ~47%, whereas CDC42b knockdown reduced uptake by ~40%; non-lipidated mutants failed to rescue, supporting localization-dependent function. (ravichandran2023thefunctionalspecificity pages 7-9) | Ravichandran 2023 | 2023-05 | https://doi.org/10.1101/2023.02.27.528078 | Mammalian cell/preprint evidence |
| quant data | In adapted ΔCdc42 mouse CTLs, transcriptomic Cdc42 log2 fold-change was -0.9448 (FDR 0.0006) and proteomic log2 fold-change was -2.7802 (FDR 0.0989); transcriptome-proteome correlation was R2 = 0.4919, p = 0.0006. (rochussen2025transcriptionaladaptationafter pages 33-34, rochussen2025transcriptionaladaptationafter pages 3-6) | Rochussen 2025 | 2025-07 | https://doi.org/10.1242/jcs.263826 | Mouse primary T-cell evidence |
| applications | Current real-world implementation is mainly experimental: mouse conditional knockout/overexpression models are used to define CDC42 roles in intestinal regeneration, epithelial barrier/polarity, hematopoietic stem-cell biology, cholangiocyte polarity, platelet regulation, and neurodevelopment. (rochussen2025transcriptionaladaptationafter pages 3-6, ravichandran2024thedistinctlocalization media a8180683, dai2023theroleof pages 1-2) | Chavez 2023; Zhou 2021; Dai 2023 | 2023-04; 2021-05; 2023-03 | https://doi.org/10.1038/s41467-023-38001-x; https://doi.org/10.7150/thno.49116; https://doi.org/10.4103/1673-5374.369101 | Strong mouse in vivo/ex vivo utility for functional annotation |
| applications | Therapeutic targeting remains exploratory. Small-GTPase targeting reviews emphasize that most Rho-family proteins, including CDC42, are still difficult to drug directly, but inhibitors and pathway-targeting strategies are being investigated; platelet-focused reviews discuss pharmacologic inhibition to modulate thrombus-related phenotypes. (yin2023targetingsmallgtpases pages 1-2, dai2023theroleof pages 1-2) | Yin 2023; Dandamudi 2023 | 2023-05; 2023-01 | https://doi.org/10.1038/s41392-023-01441-4; https://doi.org/10.3390/ijms24032519 | General/translational, not mouse-P60766-specific drug approval evidence |
Table: This table summarizes identity, molecular function, localization, pathways, quantitative findings, and applications relevant to mouse CDC42 (UniProt P60766). It uses only the evidence available in the cited context IDs and distinguishes mouse-specific findings from broader CDC42/Rho-family mechanisms.
Key 2023–2024 sources used above include:
- Bement et al., Nature Reviews Molecular Cell Biology (2024-01). https://doi.org/10.1038/s41580-023-00682-z (bement2024patterningofthe pages 1-6, bement2024patterningofthe pages 6-8)
- Ravichandran et al., The Journal of Cell Biology (2024-02). https://doi.org/10.1083/jcb.202004092 (ravichandran2024thedistinctlocalization pages 1-2, ravichandran2024thedistinctlocalization media a8180683)
- Akhtar et al., Journal of Alzheimer’s Disease (2024-11). https://doi.org/10.1177/13872877241291076 (akhtar2024spatialandplanar pages 1-3)
- Wirth & Ponimaskin, Frontiers in Physiology (2023-01). https://doi.org/10.3389/fphys.2022.1088840 (wirth2023lipidationofsmall pages 2-4)
- Yin et al., Signal Transduction and Targeted Therapy (2023-05). https://doi.org/10.1038/s41392-023-01441-4 (yin2023targetingsmallgtpases pages 1-2)
References
(dai2023theroleof pages 1-2): Yuanying Dai, Xiangming Gao, Dongqing Liu, and Jie Gong. The role of rho gtpase family in cochlear hair cells and hearing. Neural Regeneration Research, 18:2167-2172, Mar 2023. URL: https://doi.org/10.4103/1673-5374.369101, doi:10.4103/1673-5374.369101. This article has 20 citations and is from a peer-reviewed journal.
(yin2023targetingsmallgtpases pages 1-2): Guowei Yin, Jing Huang, Johnny Petela, Hongmei Jiang, Yuetong Zhang, Siqi Gong, Jiaxin Wu, Bei Liu, Jianyou Shi, and Yijun Gao. Targeting small gtpases: emerging grasps on previously untamable targets, pioneered by kras. Signal Transduction and Targeted Therapy, May 2023. URL: https://doi.org/10.1038/s41392-023-01441-4, doi:10.1038/s41392-023-01441-4. This article has 90 citations and is from a peer-reviewed journal.
(ravichandran2024thedistinctlocalization pages 1-2): Yamini Ravichandran, Jan Hänisch, Kerren Murray, Vanessa Roca, Florent Dingli, Damarys Loew, Valentin Sabatet, Batiste Boëda, Theresia E. Stradal, and Sandrine Etienne-Manneville. The distinct localization of cdc42 isoforms is responsible for their specific functions during migration. The Journal of Cell Biology, Feb 2024. URL: https://doi.org/10.1083/jcb.202004092, doi:10.1083/jcb.202004092. This article has 9 citations.
(wirth2023lipidationofsmall pages 2-4): Alexander Wirth and Evgeni Ponimaskin. Lipidation of small gtpase cdc42 as regulator of its physiological and pathophysiological functions. Frontiers in Physiology, Jan 2023. URL: https://doi.org/10.3389/fphys.2022.1088840, doi:10.3389/fphys.2022.1088840. This article has 12 citations.
(bement2024patterningofthe pages 1-6): William M. Bement, Andrew B. Goryachev, Ann L. Miller, and George von Dassow. Patterning of the cell cortex by rho gtpases. Nature reviews. Molecular cell biology, 25:290-308, Jan 2024. URL: https://doi.org/10.1038/s41580-023-00682-z, doi:10.1038/s41580-023-00682-z. This article has 142 citations.
(bement2024patterningofthe pages 6-8): William M. Bement, Andrew B. Goryachev, Ann L. Miller, and George von Dassow. Patterning of the cell cortex by rho gtpases. Nature reviews. Molecular cell biology, 25:290-308, Jan 2024. URL: https://doi.org/10.1038/s41580-023-00682-z, doi:10.1038/s41580-023-00682-z. This article has 142 citations.
(hawkins2023theautoinflammatoryc188y pages 36-40): R Whittaker Hawkins. The autoinflammatory c188y mutation in cdc42. Unknown journal, 2023.
(nishimura2013identificationofa pages 1-3): Akiyuki Nishimura and Maurine E. Linder. Identification of a novel prenyl and palmitoyl modification at the caax motif of cdc42 that regulates rhogdi binding. Molecular and Cellular Biology, 33:1417-1429, Apr 2013. URL: https://doi.org/10.1128/mcb.01398-12, doi:10.1128/mcb.01398-12. This article has 117 citations and is from a domain leading peer-reviewed journal.
(nishimura2013identificationofa pages 6-7): Akiyuki Nishimura and Maurine E. Linder. Identification of a novel prenyl and palmitoyl modification at the caax motif of cdc42 that regulates rhogdi binding. Molecular and Cellular Biology, 33:1417-1429, Apr 2013. URL: https://doi.org/10.1128/mcb.01398-12, doi:10.1128/mcb.01398-12. This article has 117 citations and is from a domain leading peer-reviewed journal.
(ravichandran2024thedistinctlocalization media a8180683): Yamini Ravichandran, Jan Hänisch, Kerren Murray, Vanessa Roca, Florent Dingli, Damarys Loew, Valentin Sabatet, Batiste Boëda, Theresia E. Stradal, and Sandrine Etienne-Manneville. The distinct localization of cdc42 isoforms is responsible for their specific functions during migration. The Journal of Cell Biology, Feb 2024. URL: https://doi.org/10.1083/jcb.202004092, doi:10.1083/jcb.202004092. This article has 9 citations.
(ravichandran2024thedistinctlocalization media 96b45e8a): Yamini Ravichandran, Jan Hänisch, Kerren Murray, Vanessa Roca, Florent Dingli, Damarys Loew, Valentin Sabatet, Batiste Boëda, Theresia E. Stradal, and Sandrine Etienne-Manneville. The distinct localization of cdc42 isoforms is responsible for their specific functions during migration. The Journal of Cell Biology, Feb 2024. URL: https://doi.org/10.1083/jcb.202004092, doi:10.1083/jcb.202004092. This article has 9 citations.
(ravichandran2024thedistinctlocalization media dd806cca): Yamini Ravichandran, Jan Hänisch, Kerren Murray, Vanessa Roca, Florent Dingli, Damarys Loew, Valentin Sabatet, Batiste Boëda, Theresia E. Stradal, and Sandrine Etienne-Manneville. The distinct localization of cdc42 isoforms is responsible for their specific functions during migration. The Journal of Cell Biology, Feb 2024. URL: https://doi.org/10.1083/jcb.202004092, doi:10.1083/jcb.202004092. This article has 9 citations.
(ravichandran2024thedistinctlocalization media 8ba5d15d): Yamini Ravichandran, Jan Hänisch, Kerren Murray, Vanessa Roca, Florent Dingli, Damarys Loew, Valentin Sabatet, Batiste Boëda, Theresia E. Stradal, and Sandrine Etienne-Manneville. The distinct localization of cdc42 isoforms is responsible for their specific functions during migration. The Journal of Cell Biology, Feb 2024. URL: https://doi.org/10.1083/jcb.202004092, doi:10.1083/jcb.202004092. This article has 9 citations.
(ravichandran2024thedistinctlocalization media 890df85d): Yamini Ravichandran, Jan Hänisch, Kerren Murray, Vanessa Roca, Florent Dingli, Damarys Loew, Valentin Sabatet, Batiste Boëda, Theresia E. Stradal, and Sandrine Etienne-Manneville. The distinct localization of cdc42 isoforms is responsible for their specific functions during migration. The Journal of Cell Biology, Feb 2024. URL: https://doi.org/10.1083/jcb.202004092, doi:10.1083/jcb.202004092. This article has 9 citations.
(ravichandran2023thefunctionalspecificity pages 4-7): Yamini Ravichandran, Jan Hänisch, Kerren Murray, Vanessa Roca, Florent Dingli, Damarys Loew, Valentin Sabatet, Batiste Boëda, Theresia Stradal, and Sandrine Etienne-Manneville. The functional specificity of cdc42 isoforms is caused by their distinct subcellular localization. bioRxiv, May 2023. URL: https://doi.org/10.1101/2023.02.27.528078, doi:10.1101/2023.02.27.528078. This article has 0 citations.
(rochussen2025transcriptionaladaptationafter pages 33-34): Adam M. Rochussen, Claire Y. Ma, and Gillian M. Griffiths. Transcriptional adaptation after deletion of cdc42 in primary t cells. Journal of cell science, Jul 2025. URL: https://doi.org/10.1242/jcs.263826, doi:10.1242/jcs.263826. This article has 4 citations and is from a domain leading peer-reviewed journal.
(ravichandran2023thefunctionalspecificity pages 7-9): Yamini Ravichandran, Jan Hänisch, Kerren Murray, Vanessa Roca, Florent Dingli, Damarys Loew, Valentin Sabatet, Batiste Boëda, Theresia Stradal, and Sandrine Etienne-Manneville. The functional specificity of cdc42 isoforms is caused by their distinct subcellular localization. bioRxiv, May 2023. URL: https://doi.org/10.1101/2023.02.27.528078, doi:10.1101/2023.02.27.528078. This article has 0 citations.
(akhtar2024spatialandplanar pages 1-3): Shayan Nik Akhtar, Tuan D Tran, Yan-Hua Chen, and Qun Lu. Spatial and planar profiling of rac1/cdc42 signaling in alzheimer's disease brain. Journal of Alzheimer's Disease, 102:670-682, Nov 2024. URL: https://doi.org/10.1177/13872877241291076, doi:10.1177/13872877241291076. This article has 4 citations and is from a peer-reviewed journal.
(rochussen2025transcriptionaladaptationafter pages 3-6): Adam M. Rochussen, Claire Y. Ma, and Gillian M. Griffiths. Transcriptional adaptation after deletion of cdc42 in primary t cells. Journal of cell science, Jul 2025. URL: https://doi.org/10.1242/jcs.263826, doi:10.1242/jcs.263826. This article has 4 citations and is from a domain leading peer-reviewed journal.
id: P60766
gene_symbol: Cdc42
product_type: PROTEIN
status: COMPLETE
taxon:
id: NCBITaxon:10090
label: Mus musculus
description: 'Cdc42 is a conserved Rho-family small GTPase that functions as a GDP/GTP-regulated
molecular switch. Active GTP-bound Cdc42 binds effectors such as WASP/N-WASP, PAK, and Par6/aPKC
polarity complexes to organize cortical actin, filopodia, cell polarity, junctions, migration,
endocytosis, cytokinesis, and spindle-related processes. Its outputs depend strongly on
membrane targeting and isoform-specific C-terminal lipidation: the broadly expressed prenylated
isoform acts at leading-edge/cortical membranes, while a brain-enriched palmitoylated isoform
contributes to intracellular membrane and neuronal contexts.'
alternative_products:
- name: 2 (Placental)
id: P60766-2, P21181-4
- name: 1 (Brain)
id: P60766-1, P21181-1
sequence_note: VSP_040585, VSP_040586
references:
- id: GO_REF:0000002
title: Gene Ontology annotation through association of InterPro records with GO terms
findings: []
- id: GO_REF:0000003
title: Gene Ontology annotation based on Enzyme Commission mapping
findings: []
- id: GO_REF:0000024
title: Manual transfer of experimentally-verified manual GO annotation data to orthologs
by curator judgment of sequence similarity
findings: []
- id: GO_REF:0000033
title: Annotation inferences using phylogenetic trees
findings: []
- id: GO_REF:0000043
title: Gene Ontology annotation based on UniProtKB/Swiss-Prot keyword mapping
findings: []
- id: GO_REF:0000044
title: Gene Ontology annotation based on UniProtKB/Swiss-Prot Subcellular Location vocabulary
mapping, accompanied by conservative changes to GO terms applied by UniProt
findings: []
- id: GO_REF:0000096
title: Automated transfer of experimentally-verified manual GO annotation data to mouse-rat
orthologs
findings: []
- id: GO_REF:0000107
title: Automatic transfer of experimentally verified manual GO annotation data to orthologs
using Ensembl Compara
findings: []
- id: GO_REF:0000117
title: Electronic Gene Ontology annotations created by ARBA machine learning models
findings: []
- id: GO_REF:0000119
title: Automated transfer of experimentally-verified manual GO annotation data to mouse-human
orthologs
findings: []
- id: GO_REF:0000120
title: Combined Automated Annotation using Multiple IEA Methods
findings: []
- id: PMID:10490598
title: The Borgs, a new family of Cdc42 and TC10 GTPase-interacting proteins.
findings: []
- id: PMID:10699171
title: Functional analysis of ARHGAP6, a novel GTPase-activating protein for RhoA.
findings: []
- id: PMID:10954424
title: The mammalian homologue of the Caenorhabditis elegans polarity protein PAR-6 is a
binding partner for the Rho GTPases Cdc42 and Rac1.
findings: []
- id: PMID:11035016
title: A new family of Cdc42 effector proteins, CEPs, function in fibroblast and epithelial
cell shape changes.
findings: []
- id: PMID:12123608
title: Plexin-B1 directly interacts with PDZ-RhoGEF/LARG to regulate RhoA and growth cone
morphology.
findings: []
- id: PMID:12637522
title: Multifunctional roles for the PH domain of Dbs in regulating Rho GTPase activation.
findings: []
- id: PMID:12773384
title: TCGAP, a multidomain Rho GTPase-activating protein involved in insulin-stimulated
glucose transport.
findings: []
- id: PMID:15249579
title: Vav GEFs are required for beta2 integrin-dependent functions of neutrophils.
findings: []
- id: PMID:15537656
title: A direct interaction between Cdc42 and vesicle-associated membrane protein 2 regulates
SNARE-dependent insulin exocytosis.
findings: []
- id: PMID:15710388
title: 'Zizimin2: a novel, DOCK180-related Cdc42 guanine nucleotide exchange factor expressed
predominantly in lymphocytes.'
findings: []
- id: PMID:15728722
title: Local phosphatidylinositol 3,4,5-trisphosphate accumulation recruits Vav2 and Vav3
to activate Rac1/Cdc42 and initiate neurite outgrowth in nerve growth factor-stimulated
PC12 cells.
findings: []
- id: PMID:15775979
title: E-cadherin is essential for in vivo epidermal barrier function by regulating tight
junctions.
findings: []
- id: PMID:15882626
title: Nuclear movement regulated by Cdc42, MRCK, myosin, and actin flow establishes MTOC
polarization in migrating cells.
findings: []
- id: PMID:15996550
title: The Rho-specific GEF Lfc interacts with neurabin and spinophilin to regulate dendritic
spine morphology.
findings: []
- id: PMID:16052498
title: Expression, synaptic localization, and developmental regulation of Ack1/Pyk1, a cytoplasmic
tyrosine kinase highly expressed in the developing and adult brain.
findings: []
- id: PMID:16621792
title: 'Membrane localization of adenomatous polyposis coli protein at cellular protrusions:
targeting sequences and regulation by beta-catenin.'
findings: []
- id: PMID:16892058
title: The Rho-GTPase cdc42 regulates neural progenitor fate at the apical surface.
findings: []
- id: PMID:17000758
title: Ccpg1, a novel scaffold protein that regulates the activity of the Rho guanine nucleotide
exchange factor Dbs.
findings: []
- id: PMID:17634366
title: Proteolipid protein is required for transport of sirtuin 2 into CNS myelin.
findings: []
- id: PMID:18325335
title: Affixin activates Rac1 via betaPIX in C2C12 myoblast.
findings: []
- id: PMID:18541910
title: Bves directly interacts with GEFT, and controls cell shape and movement through regulation
of Rac1/Cdc42 activity.
findings: []
- id: PMID:18604197
title: IQGAP3 regulates cell proliferation through the Ras/ERK signalling cascade.
findings: []
- id: PMID:18838382
title: FGD2, a CDC42-specific exchange factor expressed by antigen-presenting cells, localizes
to early endosomes and active membrane ruffles.
findings: []
- id: PMID:18854161
title: ACF7 regulates cytoskeletal-focal adhesion dynamics and migration and has ATPase
activity.
findings: []
- id: PMID:19144319
title: The phagosomal proteome in interferon-gamma-activated macrophages.
findings: []
- id: PMID:19244314
title: Cdo promotes neuronal differentiation via activation of the p38 mitogen-activated
protein kinase pathway.
findings: []
- id: PMID:19796622
title: Uncovering early response of gene regulatory networks in ESCs by systematic induction
of transcription factors.
findings: []
- id: PMID:19893577
title: The adenomatous polyposis coli-associated exchange factors Asef and Asef2 are required
for adenoma formation in Apc(Min/+)mice.
findings: []
- id: PMID:21048939
title: ARHGEF7 (Beta-PIX) acts as guanine nucleotide exchange factor for leucine-rich repeat
kinase 2.
findings: []
- id: PMID:21690310
title: Tinman/Nkx2-5 acts via miR-1 and upstream of Cdc42 to regulate heart function across
species.
findings: []
- id: PMID:21828338
title: "Cool-1/\u03B2PIX functions as a guanine nucleotide exchange factor in the cycling\
\ of Cdc42 to regulate insulin secretion."
findings: []
- id: PMID:22461490
title: DOCK8 is a Cdc42 activator critical for interstitial dendritic cell migration during
immune responses.
findings: []
- id: PMID:22494997
title: Age-related guanine nucleotide exchange factor, mouse Zizimin2, induces filopodia
in bone marrow-derived dendritic cells.
findings: []
- id: PMID:23219958
title: CDC42 is required for structural patterning of the lung during development.
findings: []
- id: PMID:23620790
title: CBAP functions as a novel component in chemokine-induced ZAP70-mediated T-cell adhesion
and migration.
findings: []
- id: PMID:23706742
title: RAS and RHO families of GTPases directly regulate distinct phosphoinositide 3-kinase
isoforms.
findings: []
- id: PMID:23793062
title: The lymphoid lineage-specific actin-uncapping protein Rltpr is essential for costimulation
via CD28 and the development of regulatory T cells.
findings: []
- id: PMID:24076653
title: CDC42 switches IRSp53 from inhibition of actin growth to elongation by clustering
of VASP.
findings: []
- id: PMID:24792215
title: CLN3 deficient cells display defects in the ARF1-Cdc42 pathway and actin-dependent
events.
findings: []
- id: PMID:25197047
title: Essential role of sympathetic endothelin A receptors for adverse cardiac remodeling.
findings: []
- id: PMID:25217619
title: Phosphoinositide 3-kinase p85beta regulates invadopodium formation.
findings: []
- id: PMID:25851601
title: The RhoGEF DOCK10 is essential for dendritic spine morphogenesis.
findings: []
- id: PMID:27917469
title: Association of dysfunctional synapse defective 1 (SYDE1) with restricted fetal growth
- SYDE1 regulates placental cell migration and invasion.
findings: []
- id: PMID:31219639
title: Cdc42 activation by endothelin regulates neural crest cell migration in the cardiac
outflow tract.
findings: []
- id: PMID:33531495
title: Photoactivatable CaMKII induces synaptic plasticity in single synapses.
findings: []
- id: PMID:37140151
title: Biallelic variants in IQCN cause sperm flagellar assembly defects and male infertility.
findings: []
- id: PMID:8464478
title: Oncogene ect2 is related to regulators of small GTP-binding proteins.
findings: []
- id: Reactome:R-MMU-3928643
title: Activation of CDC42 by intersectin-1
findings: []
- id: Reactome:R-MMU-442572
title: Activation of WASP and N-WASP by CDC42
findings: []
- id: Reactome:R-MMU-448947
title: Interaction of Bnip-2 with Cdc42
findings: []
- id: Reactome:R-MMU-5665684
title: Fmnl1 binds Cdc42:GTP
findings: []
- id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
title: Falcon deep research summary for mouse Cdc42
findings: []
existing_annotations:
- term:
id: GO:0003924
label: GTPase activity
evidence_type: IBA
original_reference_id: GO_REF:0000033
review:
summary: GTPase activity is consistent with core Cdc42 GTPase, cytoskeletal, polarity,
or localization biology.
action: ACCEPT
reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane
localization, or immediate actin/polarity outputs.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: CDC42 is a **GTP-hydrolyzing enzyme** (small GTPase). Its substrate
is **GTP**, which it binds and hydrolyzes to **GDP + Pi**
- term:
id: GO:0005525
label: GTP binding
evidence_type: IBA
original_reference_id: GO_REF:0000033
review:
summary: GTP binding is consistent with core Cdc42 GTPase, cytoskeletal, polarity, or
localization biology.
action: ACCEPT
reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane
localization, or immediate actin/polarity outputs.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: CDC42 is a **GTP-hydrolyzing enzyme** (small GTPase). Its substrate
is **GTP**, which it binds and hydrolyzes to **GDP + Pi**
- term:
id: GO:0007165
label: signal transduction
evidence_type: IBA
original_reference_id: GO_REF:0000033
review:
summary: signal transduction is a broad ancestor for the Cdc42 signaling role.
action: MODIFY
reason: Cdc42 is best represented as a small GTPase/Rho-family signaling switch.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: CDC42 belongs to the **Rho family** of small GTPases and acts as a
**molecular switch** cycling between **GTP-bound (active)** and **GDP-bound (inactive)**
states
proposed_replacement_terms:
- &id001
id: GO:0007264
label: small GTPase-mediated signal transduction
- term:
id: GO:0005886
label: plasma membrane
evidence_type: IBA
original_reference_id: GO_REF:0000033
review:
summary: plasma membrane is consistent with core Cdc42 GTPase, cytoskeletal, polarity,
or localization biology.
action: ACCEPT
reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane
localization, or immediate actin/polarity outputs.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: CDC42 associates with the **plasma membrane/cell cortex** via a **carboxy-terminal
prenyl group**
- term:
id: GO:0007015
label: actin filament organization
evidence_type: IBA
original_reference_id: GO_REF:0000033
review:
summary: actin filament organization is consistent with core Cdc42 GTPase, cytoskeletal,
polarity, or localization biology.
action: ACCEPT
reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane
localization, or immediate actin/polarity outputs.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: CDC42 is directly linked to actin nucleation pathways through **WASP-family
nucleation-promoting factors**.
- term:
id: GO:0030010
label: establishment of cell polarity
evidence_type: IBA
original_reference_id: GO_REF:0000033
review:
summary: establishment of cell polarity is consistent with core Cdc42 GTPase, cytoskeletal,
polarity, or localization biology.
action: ACCEPT
reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane
localization, or immediate actin/polarity outputs.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: CDC42b supports **N-WASP-mediated endocytosis** from intracellular
compartments.
- term:
id: GO:0006897
label: endocytosis
evidence_type: IBA
original_reference_id: GO_REF:0000033
review:
summary: endocytosis is a supported Cdc42 cellular output, but it is not the core small
GTPase catalytic function.
action: KEEP_AS_NON_CORE
reason: Cdc42 GTP-bound effector signaling can influence trafficking and membrane dynamics,
but this process should be treated as context-specific.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: In its **GTP-bound state**, CDC42 binds effector proteins that drive
downstream cytoskeletal and polarity responses
- term:
id: GO:0019901
label: protein kinase binding
evidence_type: IBA
original_reference_id: GO_REF:0000033
review:
summary: protein kinase binding is consistent with core Cdc42 GTPase, cytoskeletal, polarity,
or localization biology.
action: ACCEPT
reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane
localization, or immediate actin/polarity outputs.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: CDC42 is directly linked to actin nucleation pathways through **WASP-family
nucleation-promoting factors**.
- term:
id: GO:0051489
label: regulation of filopodium assembly
evidence_type: IBA
original_reference_id: GO_REF:0000033
review:
summary: regulation of filopodium assembly is consistent with core Cdc42 GTPase, cytoskeletal,
polarity, or localization biology.
action: ACCEPT
reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane
localization, or immediate actin/polarity outputs.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: CDC42 is directly linked to actin nucleation pathways through **WASP-family
nucleation-promoting factors**.
- term:
id: GO:0000166
label: nucleotide binding
evidence_type: IEA
original_reference_id: GO_REF:0000043
review:
summary: Nucleotide binding is too broad for Cdc42.
action: MODIFY
reason: Cdc42 specifically binds guanine nucleotides and functions through GTP/GDP cycling.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: CDC42 is a **GTP-hydrolyzing enzyme** (small GTPase). Its substrate
is **GTP**, which it binds and hydrolyzes to **GDP + Pi**
proposed_replacement_terms:
- id: GO:0005525
label: GTP binding
- term:
id: GO:0003924
label: GTPase activity
evidence_type: IEA
original_reference_id: GO_REF:0000120
review:
summary: GTPase activity is consistent with core Cdc42 GTPase, cytoskeletal, polarity,
or localization biology.
action: ACCEPT
reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane
localization, or immediate actin/polarity outputs.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: CDC42 is a **GTP-hydrolyzing enzyme** (small GTPase). Its substrate
is **GTP**, which it binds and hydrolyzes to **GDP + Pi**
- term:
id: GO:0003925
label: G protein activity
evidence_type: IEA
original_reference_id: GO_REF:0000003
review:
summary: G protein activity is consistent with core Cdc42 GTPase, cytoskeletal, polarity,
or localization biology.
action: ACCEPT
reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane
localization, or immediate actin/polarity outputs.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: CDC42 is a **GTP-hydrolyzing enzyme** (small GTPase). Its substrate
is **GTP**, which it binds and hydrolyzes to **GDP + Pi**
- term:
id: GO:0005525
label: GTP binding
evidence_type: IEA
original_reference_id: GO_REF:0000120
review:
summary: GTP binding is consistent with core Cdc42 GTPase, cytoskeletal, polarity, or
localization biology.
action: ACCEPT
reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane
localization, or immediate actin/polarity outputs.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: CDC42 is a **GTP-hydrolyzing enzyme** (small GTPase). Its substrate
is **GTP**, which it binds and hydrolyzes to **GDP + Pi**
- term:
id: GO:0005737
label: cytoplasm
evidence_type: IEA
original_reference_id: GO_REF:0000120
review:
summary: cytoplasm is consistent with core Cdc42 GTPase, cytoskeletal, polarity, or localization
biology.
action: ACCEPT
reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane
localization, or immediate actin/polarity outputs.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: CDC42 associates with the **plasma membrane/cell cortex** via a **carboxy-terminal
prenyl group**
- term:
id: GO:0005813
label: centrosome
evidence_type: IEA
original_reference_id: GO_REF:0000120
review:
summary: centrosome is consistent with core Cdc42 GTPase, cytoskeletal, polarity, or localization
biology.
action: ACCEPT
reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane
localization, or immediate actin/polarity outputs.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: CDC42 is directly linked to actin nucleation pathways through **WASP-family
nucleation-promoting factors**.
- term:
id: GO:0005819
label: spindle
evidence_type: IEA
original_reference_id: GO_REF:0000044
review:
summary: This automated generic cellular-component transfer is too broad relative
to the narrower Cdc42 localization annotations retained elsewhere.
action: REMOVE
reason: The local evidence does not justify keeping this broad automated component
row as a separate accepted annotation; it was previously supported only by
unrelated actin-effector biology.
- term:
id: GO:0005886
label: plasma membrane
evidence_type: IEA
original_reference_id: GO_REF:0000120
review:
summary: plasma membrane is consistent with core Cdc42 GTPase, cytoskeletal, polarity,
or localization biology.
action: ACCEPT
reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane
localization, or immediate actin/polarity outputs.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: CDC42 associates with the **plasma membrane/cell cortex** via a **carboxy-terminal
prenyl group**
- term:
id: GO:0007264
label: small GTPase-mediated signal transduction
evidence_type: IEA
original_reference_id: GO_REF:0000002
review:
summary: small GTPase-mediated signal transduction is consistent with core Cdc42 GTPase,
cytoskeletal, polarity, or localization biology.
action: ACCEPT
reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane
localization, or immediate actin/polarity outputs.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: CDC42 is directly linked to actin nucleation pathways through **WASP-family
nucleation-promoting factors**.
- term:
id: GO:0007399
label: nervous system development
evidence_type: IEA
original_reference_id: GO_REF:0000043
review:
summary: nervous system development is a supported context-specific Cdc42 output.
action: KEEP_AS_NON_CORE
reason: Cdc42 controls broad cellular architecture and developmental programs through
actin, polarity, trafficking, and kinase-effector pathways, but this term is not the
core molecular function.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: In its **GTP-bound state**, CDC42 binds effector proteins that drive
downstream cytoskeletal and polarity responses
- term:
id: GO:0009653
label: anatomical structure morphogenesis
evidence_type: IEA
original_reference_id: GO_REF:0000117
review:
summary: anatomical structure morphogenesis is a supported context-specific Cdc42 output.
action: KEEP_AS_NON_CORE
reason: Cdc42 controls broad cellular architecture and developmental programs through
actin, polarity, trafficking, and kinase-effector pathways, but this term is not the
core molecular function.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: In its **GTP-bound state**, CDC42 binds effector proteins that drive
downstream cytoskeletal and polarity responses
- term:
id: GO:0016787
label: hydrolase activity
evidence_type: IEA
original_reference_id: GO_REF:0000043
review:
summary: Hydrolase activity is too broad for Cdc42.
action: MODIFY
reason: The relevant hydrolytic activity is GTPase activity in a Rho-family molecular
switch.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: CDC42 is a **GTP-hydrolyzing enzyme** (small GTPase). Its substrate
is **GTP**, which it binds and hydrolyzes to **GDP + Pi**
proposed_replacement_terms:
- &id002
id: GO:0003924
label: GTPase activity
- term:
id: GO:0030154
label: cell differentiation
evidence_type: IEA
original_reference_id: GO_REF:0000043
review:
summary: cell differentiation is a supported context-specific Cdc42 output.
action: KEEP_AS_NON_CORE
reason: Cdc42 controls broad cellular architecture and developmental programs through
actin, polarity, trafficking, and kinase-effector pathways, but this term is not the
core molecular function.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: In its **GTP-bound state**, CDC42 binds effector proteins that drive
downstream cytoskeletal and polarity responses
- term:
id: GO:0030425
label: dendrite
evidence_type: IEA
original_reference_id: GO_REF:0000044
review:
summary: dendrite is a supported context-specific Cdc42 output.
action: KEEP_AS_NON_CORE
reason: Cdc42 controls broad cellular architecture and developmental programs through
actin, polarity, trafficking, and kinase-effector pathways, but this term is not the
core molecular function.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: In its **GTP-bound state**, CDC42 binds effector proteins that drive
downstream cytoskeletal and polarity responses
- term:
id: GO:0030496
label: midbody
evidence_type: IEA
original_reference_id: GO_REF:0000120
review:
summary: midbody is consistent with core Cdc42 GTPase, cytoskeletal, polarity, or localization
biology.
action: ACCEPT
reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane
localization, or immediate actin/polarity outputs.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: CDC42 is directly linked to actin nucleation pathways through **WASP-family
nucleation-promoting factors**.
- term:
id: GO:0031258
label: lamellipodium membrane
evidence_type: IEA
original_reference_id: GO_REF:0000044
review:
summary: lamellipodium membrane is consistent with core Cdc42 GTPase, cytoskeletal, polarity,
or localization biology.
action: ACCEPT
reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane
localization, or immediate actin/polarity outputs.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: CDC42 is directly linked to actin nucleation pathways through **WASP-family
nucleation-promoting factors**.
- term:
id: GO:0051130
label: positive regulation of cellular component organization
evidence_type: IEA
original_reference_id: GO_REF:0000117
review:
summary: positive regulation of cellular component organization is a supported context-specific
Cdc42 output.
action: KEEP_AS_NON_CORE
reason: Cdc42 controls broad cellular architecture and developmental programs through
actin, polarity, trafficking, and kinase-effector pathways, but this term is not the
core molecular function.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: In its **GTP-bound state**, CDC42 binds effector proteins that drive
downstream cytoskeletal and polarity responses
- term:
id: GO:0071944
label: cell periphery
evidence_type: IEA
original_reference_id: GO_REF:0000117
review:
summary: cell periphery is consistent with core Cdc42 GTPase, cytoskeletal, polarity,
or localization biology.
action: ACCEPT
reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane
localization, or immediate actin/polarity outputs.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: CDC42 associates with the **plasma membrane/cell cortex** via a **carboxy-terminal
prenyl group**
- term:
id: GO:0005515
label: protein binding
evidence_type: IPI
original_reference_id: PMID:12123608
review:
summary: protein binding records a physical association but is too generic to describe
the gene product function.
action: MARK_AS_OVER_ANNOTATED
reason: The evidence supports regulated signaling-complex assembly, not a meaningful standalone
protein binding function; more informative molecular and pathway terms capture the biology.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: In its **GTP-bound state**, CDC42 binds effector proteins that drive
downstream cytoskeletal and polarity responses
- term:
id: GO:0005515
label: protein binding
evidence_type: IPI
original_reference_id: PMID:15537656
review:
summary: protein binding records a physical association but is too generic to describe
the gene product function.
action: MARK_AS_OVER_ANNOTATED
reason: The evidence supports regulated signaling-complex assembly, not a meaningful standalone
protein binding function; more informative molecular and pathway terms capture the biology.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: In its **GTP-bound state**, CDC42 binds effector proteins that drive
downstream cytoskeletal and polarity responses
- term:
id: GO:0005515
label: protein binding
evidence_type: IPI
original_reference_id: PMID:18325335
review:
summary: protein binding records a physical association but is too generic to describe
the gene product function.
action: MARK_AS_OVER_ANNOTATED
reason: The evidence supports regulated signaling-complex assembly, not a meaningful standalone
protein binding function; more informative molecular and pathway terms capture the biology.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: In its **GTP-bound state**, CDC42 binds effector proteins that drive
downstream cytoskeletal and polarity responses
- term:
id: GO:0005515
label: protein binding
evidence_type: IPI
original_reference_id: PMID:18541910
review:
summary: protein binding records a physical association but is too generic to describe
the gene product function.
action: MARK_AS_OVER_ANNOTATED
reason: The evidence supports regulated signaling-complex assembly, not a meaningful standalone
protein binding function; more informative molecular and pathway terms capture the biology.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: In its **GTP-bound state**, CDC42 binds effector proteins that drive
downstream cytoskeletal and polarity responses
- term:
id: GO:0005515
label: protein binding
evidence_type: IPI
original_reference_id: PMID:18854161
review:
summary: protein binding records a physical association but is too generic to describe
the gene product function.
action: MARK_AS_OVER_ANNOTATED
reason: The evidence supports regulated signaling-complex assembly, not a meaningful standalone
protein binding function; more informative molecular and pathway terms capture the biology.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: In its **GTP-bound state**, CDC42 binds effector proteins that drive
downstream cytoskeletal and polarity responses
- term:
id: GO:0005515
label: protein binding
evidence_type: IPI
original_reference_id: PMID:19893577
review:
summary: protein binding records a physical association but is too generic to describe
the gene product function.
action: MARK_AS_OVER_ANNOTATED
reason: The evidence supports regulated signaling-complex assembly, not a meaningful standalone
protein binding function; more informative molecular and pathway terms capture the biology.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: In its **GTP-bound state**, CDC42 binds effector proteins that drive
downstream cytoskeletal and polarity responses
- term:
id: GO:0005515
label: protein binding
evidence_type: IPI
original_reference_id: PMID:23706742
review:
summary: protein binding records a physical association but is too generic to describe
the gene product function.
action: MARK_AS_OVER_ANNOTATED
reason: The evidence supports regulated signaling-complex assembly, not a meaningful standalone
protein binding function; more informative molecular and pathway terms capture the biology.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: In its **GTP-bound state**, CDC42 binds effector proteins that drive
downstream cytoskeletal and polarity responses
- term:
id: GO:0006911
label: phagocytosis, engulfment
evidence_type: IEA
original_reference_id: GO_REF:0000107
review:
summary: phagocytosis, engulfment is consistent with core Cdc42 GTPase, cytoskeletal,
polarity, or localization biology.
action: ACCEPT
reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane
localization, or immediate actin/polarity outputs.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: CDC42 is directly linked to actin nucleation pathways through **WASP-family
nucleation-promoting factors**.
- term:
id: GO:0007015
label: actin filament organization
evidence_type: IEA
original_reference_id: GO_REF:0000107
review:
summary: actin filament organization is consistent with core Cdc42 GTPase, cytoskeletal,
polarity, or localization biology.
action: ACCEPT
reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane
localization, or immediate actin/polarity outputs.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: CDC42 is directly linked to actin nucleation pathways through **WASP-family
nucleation-promoting factors**.
- term:
id: GO:0007229
label: integrin-mediated signaling pathway
evidence_type: IEA
original_reference_id: GO_REF:0000107
review:
summary: integrin-mediated signaling pathway is a supported context-specific Cdc42 output.
action: KEEP_AS_NON_CORE
reason: Cdc42 controls broad cellular architecture and developmental programs through
actin, polarity, trafficking, and kinase-effector pathways, but this term is not the
core molecular function.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: In its **GTP-bound state**, CDC42 binds effector proteins that drive
downstream cytoskeletal and polarity responses
- term:
id: GO:0010591
label: regulation of lamellipodium assembly
evidence_type: IEA
original_reference_id: GO_REF:0000107
review:
summary: regulation of lamellipodium assembly is consistent with core Cdc42 GTPase, cytoskeletal,
polarity, or localization biology.
action: ACCEPT
reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane
localization, or immediate actin/polarity outputs.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: CDC42 is directly linked to actin nucleation pathways through **WASP-family
nucleation-promoting factors**.
- term:
id: GO:0010592
label: positive regulation of lamellipodium assembly
evidence_type: IEA
original_reference_id: GO_REF:0000107
review:
summary: positive regulation of lamellipodium assembly is consistent with core Cdc42 GTPase,
cytoskeletal, polarity, or localization biology.
action: ACCEPT
reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane
localization, or immediate actin/polarity outputs.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: CDC42 is directly linked to actin nucleation pathways through **WASP-family
nucleation-promoting factors**.
- term:
id: GO:0015630
label: microtubule cytoskeleton
evidence_type: IEA
original_reference_id: GO_REF:0000107
review:
summary: microtubule cytoskeleton is a supported context-specific Cdc42 output.
action: KEEP_AS_NON_CORE
reason: Cdc42 controls broad cellular architecture and developmental programs through
actin, polarity, trafficking, and kinase-effector pathways, but this term is not the
core molecular function.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: In its **GTP-bound state**, CDC42 binds effector proteins that drive
downstream cytoskeletal and polarity responses
- term:
id: GO:0016020
label: membrane
evidence_type: IEA
original_reference_id: GO_REF:0000107
review:
summary: membrane is consistent with core Cdc42 GTPase, cytoskeletal, polarity, or localization
biology.
action: ACCEPT
reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane
localization, or immediate actin/polarity outputs.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: CDC42 associates with the **plasma membrane/cell cortex** via a **carboxy-terminal
prenyl group**
- term:
id: GO:0017119
label: Golgi transport complex
evidence_type: IEA
original_reference_id: GO_REF:0000107
review:
summary: Golgi transport complex is a supported context-specific Cdc42 output.
action: KEEP_AS_NON_CORE
reason: Cdc42 controls broad cellular architecture and developmental programs through
actin, polarity, trafficking, and kinase-effector pathways, but this term is not the
core molecular function.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: In its **GTP-bound state**, CDC42 binds effector proteins that drive
downstream cytoskeletal and polarity responses
- term:
id: GO:0019901
label: protein kinase binding
evidence_type: IEA
original_reference_id: GO_REF:0000120
review:
summary: protein kinase binding is consistent with core Cdc42 GTPase, cytoskeletal, polarity,
or localization biology.
action: ACCEPT
reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane
localization, or immediate actin/polarity outputs.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: CDC42 is directly linked to actin nucleation pathways through **WASP-family
nucleation-promoting factors**.
- term:
id: GO:0030036
label: actin cytoskeleton organization
evidence_type: IEA
original_reference_id: GO_REF:0000107
review:
summary: actin cytoskeleton organization is consistent with core Cdc42 GTPase, cytoskeletal,
polarity, or localization biology.
action: ACCEPT
reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane
localization, or immediate actin/polarity outputs.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: CDC42 is directly linked to actin nucleation pathways through **WASP-family
nucleation-promoting factors**.
- term:
id: GO:0030175
label: filopodium
evidence_type: IEA
original_reference_id: GO_REF:0000107
review:
summary: filopodium is consistent with core Cdc42 GTPase, cytoskeletal, polarity, or localization
biology.
action: ACCEPT
reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane
localization, or immediate actin/polarity outputs.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: CDC42 is directly linked to actin nucleation pathways through **WASP-family
nucleation-promoting factors**.
- term:
id: GO:0030307
label: positive regulation of cell growth
evidence_type: IEA
original_reference_id: GO_REF:0000107
review:
summary: positive regulation of cell growth is a supported context-specific Cdc42 output.
action: KEEP_AS_NON_CORE
reason: Cdc42 controls broad cellular architecture and developmental programs through
actin, polarity, trafficking, and kinase-effector pathways, but this term is not the
core molecular function.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: In its **GTP-bound state**, CDC42 binds effector proteins that drive
downstream cytoskeletal and polarity responses
- term:
id: GO:0030335
label: positive regulation of cell migration
evidence_type: IEA
original_reference_id: GO_REF:0000107
review:
summary: positive regulation of cell migration is a supported context-specific Cdc42 output.
action: KEEP_AS_NON_CORE
reason: Cdc42 controls broad cellular architecture and developmental programs through
actin, polarity, trafficking, and kinase-effector pathways, but this term is not the
core molecular function.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: In its **GTP-bound state**, CDC42 binds effector proteins that drive
downstream cytoskeletal and polarity responses
- term:
id: GO:0031274
label: positive regulation of pseudopodium assembly
evidence_type: IEA
original_reference_id: GO_REF:0000107
review:
summary: positive regulation of pseudopodium assembly is consistent with core Cdc42 GTPase,
cytoskeletal, polarity, or localization biology.
action: ACCEPT
reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane
localization, or immediate actin/polarity outputs.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: CDC42 is directly linked to actin nucleation pathways through **WASP-family
nucleation-promoting factors**.
- term:
id: GO:0031333
label: negative regulation of protein-containing complex assembly
evidence_type: IEA
original_reference_id: GO_REF:0000107
review:
summary: negative regulation of protein-containing complex assembly is a supported context-specific
Cdc42 output.
action: KEEP_AS_NON_CORE
reason: Cdc42 controls broad cellular architecture and developmental programs through
actin, polarity, trafficking, and kinase-effector pathways, but this term is not the
core molecular function.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: In its **GTP-bound state**, CDC42 binds effector proteins that drive
downstream cytoskeletal and polarity responses
- term:
id: GO:0031996
label: thioesterase binding
evidence_type: IEA
original_reference_id: GO_REF:0000107
review:
summary: thioesterase binding is a supported context-specific Cdc42 output.
action: KEEP_AS_NON_CORE
reason: Cdc42 controls broad cellular architecture and developmental programs through
actin, polarity, trafficking, and kinase-effector pathways, but this term is not the
core molecular function.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: In its **GTP-bound state**, CDC42 binds effector proteins that drive
downstream cytoskeletal and polarity responses
- term:
id: GO:0032427
label: GBD domain binding
evidence_type: IEA
original_reference_id: GO_REF:0000107
review:
summary: GBD domain binding is consistent with core Cdc42 GTPase, cytoskeletal, polarity,
or localization biology.
action: ACCEPT
reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane
localization, or immediate actin/polarity outputs.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: CDC42 is directly linked to actin nucleation pathways through **WASP-family
nucleation-promoting factors**.
- term:
id: GO:0032467
label: positive regulation of cytokinesis
evidence_type: IEA
original_reference_id: GO_REF:0000107
review:
summary: positive regulation of cytokinesis is supported for Cdc42, but this is a cell-cycle
output rather than the small GTPase catalytic role itself.
action: ACCEPT
reason: UniProt carries this transferred process annotation, but it is treated as a
downstream cell-cycle output rather than core GTPase catalysis.
supported_by:
- reference_id: UniProt:P60766
supporting_text: 'GO; GO:0032467; P:positive regulation of cytokinesis; ISS:UniProtKB.'
- term:
id: GO:0032956
label: regulation of actin cytoskeleton organization
evidence_type: IEA
original_reference_id: GO_REF:0000107
review:
summary: regulation of actin cytoskeleton organization is a supported context-specific
Cdc42 output.
action: KEEP_AS_NON_CORE
reason: Cdc42 controls broad cellular architecture and developmental programs through
actin, polarity, trafficking, and kinase-effector pathways, but this term is not the
core molecular function.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: In its **GTP-bound state**, CDC42 binds effector proteins that drive
downstream cytoskeletal and polarity responses
- term:
id: GO:0032991
label: protein-containing complex
evidence_type: IEA
original_reference_id: GO_REF:0000107
review:
summary: protein-containing complex is a supported context-specific Cdc42 output.
action: KEEP_AS_NON_CORE
reason: Cdc42 controls broad cellular architecture and developmental programs through
actin, polarity, trafficking, and kinase-effector pathways, but this term is not the
core molecular function.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: In its **GTP-bound state**, CDC42 binds effector proteins that drive
downstream cytoskeletal and polarity responses
- term:
id: GO:0034191
label: apolipoprotein A-I receptor binding
evidence_type: IEA
original_reference_id: GO_REF:0000107
review:
summary: apolipoprotein A-I receptor binding is a supported context-specific Cdc42 output.
action: KEEP_AS_NON_CORE
reason: Cdc42 controls broad cellular architecture and developmental programs through
actin, polarity, trafficking, and kinase-effector pathways, but this term is not the
core molecular function.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: In its **GTP-bound state**, CDC42 binds effector proteins that drive
downstream cytoskeletal and polarity responses
- term:
id: GO:0034329
label: cell junction assembly
evidence_type: IEA
original_reference_id: GO_REF:0000107
review:
summary: cell junction assembly is a supported context-specific Cdc42 output.
action: KEEP_AS_NON_CORE
reason: Cdc42 controls broad cellular architecture and developmental programs through
actin, polarity, trafficking, and kinase-effector pathways, but this term is not the
core molecular function.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: In its **GTP-bound state**, CDC42 binds effector proteins that drive
downstream cytoskeletal and polarity responses
- term:
id: GO:0036464
label: cytoplasmic ribonucleoprotein granule
evidence_type: IEA
original_reference_id: GO_REF:0000107
review:
summary: cytoplasmic ribonucleoprotein granule is retained as a non-core Cdc42-associated
annotation.
action: KEEP_AS_NON_CORE
reason: The annotation is plausible as a downstream or compartment-specific consequence
of Cdc42 signaling rather than the core GTPase switch activity.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: In its **GTP-bound state**, CDC42 binds effector proteins that drive
downstream cytoskeletal and polarity responses
- term:
id: GO:0038189
label: neuropilin signaling pathway
evidence_type: IEA
original_reference_id: GO_REF:0000107
review:
summary: neuropilin signaling pathway is a supported context-specific Cdc42 output.
action: KEEP_AS_NON_CORE
reason: Cdc42 controls broad cellular architecture and developmental programs through
actin, polarity, trafficking, and kinase-effector pathways, but this term is not the
core molecular function.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: In its **GTP-bound state**, CDC42 binds effector proteins that drive
downstream cytoskeletal and polarity responses
- term:
id: GO:0042802
label: identical protein binding
evidence_type: IEA
original_reference_id: GO_REF:0000107
review:
summary: identical protein binding is a supported context-specific Cdc42 output.
action: KEEP_AS_NON_CORE
reason: Cdc42 controls broad cellular architecture and developmental programs through
actin, polarity, trafficking, and kinase-effector pathways, but this term is not the
core molecular function.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: In its **GTP-bound state**, CDC42 binds effector proteins that drive
downstream cytoskeletal and polarity responses
- term:
id: GO:0043005
label: neuron projection
evidence_type: IEA
original_reference_id: GO_REF:0000107
review:
summary: neuron projection is a supported context-specific Cdc42 output.
action: KEEP_AS_NON_CORE
reason: Cdc42 controls broad cellular architecture and developmental programs through
actin, polarity, trafficking, and kinase-effector pathways, but this term is not the
core molecular function.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: In its **GTP-bound state**, CDC42 binds effector proteins that drive
downstream cytoskeletal and polarity responses
- term:
id: GO:0043025
label: neuronal cell body
evidence_type: IEA
original_reference_id: GO_REF:0000107
review:
summary: neuronal cell body is a supported context-specific Cdc42 output.
action: KEEP_AS_NON_CORE
reason: Cdc42 controls broad cellular architecture and developmental programs through
actin, polarity, trafficking, and kinase-effector pathways, but this term is not the
core molecular function.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: In its **GTP-bound state**, CDC42 binds effector proteins that drive
downstream cytoskeletal and polarity responses
- term:
id: GO:0044788
label: host-mediated perturbation of viral process
evidence_type: IEA
original_reference_id: GO_REF:0000107
review:
summary: host-mediated perturbation of viral process is a supported context-specific Cdc42
output.
action: KEEP_AS_NON_CORE
reason: Cdc42 controls broad cellular architecture and developmental programs through
actin, polarity, trafficking, and kinase-effector pathways, but this term is not the
core molecular function.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: In its **GTP-bound state**, CDC42 binds effector proteins that drive
downstream cytoskeletal and polarity responses
- term:
id: GO:0045198
label: establishment of epithelial cell apical/basal polarity
evidence_type: IEA
original_reference_id: GO_REF:0000107
review:
summary: establishment of epithelial cell apical/basal polarity is consistent with core
Cdc42 GTPase, cytoskeletal, polarity, or localization biology.
action: ACCEPT
reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane
localization, or immediate actin/polarity outputs.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: In its **GTP-bound state**, CDC42 binds effector proteins that drive
downstream cytoskeletal and polarity responses
- term:
id: GO:0051233
label: spindle midzone
evidence_type: IEA
original_reference_id: GO_REF:0000107
review:
summary: spindle midzone is consistent with core Cdc42 GTPase, cytoskeletal, polarity,
or localization biology.
action: ACCEPT
reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane
localization, or immediate actin/polarity outputs.
supported_by:
- reference_id: UniProt:P60766
supporting_text: Moves to the central spindle as cells progressed through anaphase to telophase.
- term:
id: GO:0051489
label: regulation of filopodium assembly
evidence_type: IEA
original_reference_id: GO_REF:0000107
review:
summary: regulation of filopodium assembly is consistent with core Cdc42 GTPase, cytoskeletal,
polarity, or localization biology.
action: ACCEPT
reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane
localization, or immediate actin/polarity outputs.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: CDC42 is directly linked to actin nucleation pathways through **WASP-family
nucleation-promoting factors**.
- term:
id: GO:0051491
label: positive regulation of filopodium assembly
evidence_type: IEA
original_reference_id: GO_REF:0000107
review:
summary: positive regulation of filopodium assembly is consistent with core Cdc42 GTPase,
cytoskeletal, polarity, or localization biology.
action: ACCEPT
reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane
localization, or immediate actin/polarity outputs.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: CDC42 is directly linked to actin nucleation pathways through **WASP-family
nucleation-promoting factors**.
- term:
id: GO:0051492
label: regulation of stress fiber assembly
evidence_type: IEA
original_reference_id: GO_REF:0000107
review:
summary: The stress-fiber wording is too specific for the available Cdc42 evidence; the
supported biology is broader actin organization through Cdc42 effector pathways.
action: MODIFY
reason: Use a broader actin-organization term rather than treating stress-fiber assembly
as a core Cdc42 output.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: CDC42 is directly linked to actin nucleation pathways through **WASP-family
nucleation-promoting factors**.
proposed_replacement_terms:
- id: GO:0007015
label: actin filament organization
- term:
id: GO:0051496
label: positive regulation of stress fiber assembly
evidence_type: IEA
original_reference_id: GO_REF:0000107
review:
summary: The stress-fiber wording is too specific for the available Cdc42 evidence; the
supported biology is broader actin organization through Cdc42 effector pathways.
action: MODIFY
reason: Use a broader actin-organization term rather than treating stress-fiber assembly
as a core Cdc42 output.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: CDC42 is directly linked to actin nucleation pathways through **WASP-family
nucleation-promoting factors**.
proposed_replacement_terms:
- id: GO:0007015
label: actin filament organization
- term:
id: GO:0051988
label: regulation of attachment of spindle microtubules to kinetochore
evidence_type: IEA
original_reference_id: GO_REF:0000107
review:
summary: regulation of attachment of spindle microtubules to kinetochore is consistent
with core Cdc42 GTPase, cytoskeletal, polarity, or localization biology.
action: ACCEPT
reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane
localization, or immediate actin/polarity outputs.
supported_by:
- reference_id: UniProt:P60766
supporting_text: Regulates the bipolar attachment of spindle microtubules to kinetochores
before chromosome congression in metaphase.
- term:
id: GO:0061630
label: ubiquitin protein ligase activity
evidence_type: IEA
original_reference_id: GO_REF:0000107
review:
summary: Cdc42 is a small GTPase, not a ubiquitin-protein ligase.
action: REMOVE
reason: No direct evidence supports assigning E3 ligase catalytic activity to Cdc42; this
appears to be an over-transfer from associated pathways or interactors.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: CDC42 is a **GTP-hydrolyzing enzyme** (small GTPase). Its substrate
is **GTP**, which it binds and hydrolyzes to **GDP + Pi**
- term:
id: GO:0072686
label: mitotic spindle
evidence_type: IEA
original_reference_id: GO_REF:0000107
review:
summary: mitotic spindle is consistent with core Cdc42 GTPase, cytoskeletal, polarity,
or localization biology.
action: ACCEPT
reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane
localization, or immediate actin/polarity outputs.
supported_by:
- reference_id: UniProt:P60766
supporting_text: Cytoplasm, cytoskeleton, spindle
- term:
id: GO:1900026
label: positive regulation of substrate adhesion-dependent cell spreading
evidence_type: IEA
original_reference_id: GO_REF:0000107
review:
summary: positive regulation of substrate adhesion-dependent cell spreading is a supported
context-specific Cdc42 output.
action: KEEP_AS_NON_CORE
reason: Cdc42 controls broad cellular architecture and developmental programs through
actin, polarity, trafficking, and kinase-effector pathways, but this term is not the
core molecular function.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: In its **GTP-bound state**, CDC42 binds effector proteins that drive
downstream cytoskeletal and polarity responses
- term:
id: GO:0015630
label: microtubule cytoskeleton
evidence_type: ISO
original_reference_id: GO_REF:0000119
review:
summary: microtubule cytoskeleton is a supported context-specific Cdc42 output.
action: KEEP_AS_NON_CORE
reason: Cdc42 controls broad cellular architecture and developmental programs through
actin, polarity, trafficking, and kinase-effector pathways, but this term is not the
core molecular function.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: In its **GTP-bound state**, CDC42 binds effector proteins that drive
downstream cytoskeletal and polarity responses
- term:
id: GO:0043085
label: positive regulation of catalytic activity
evidence_type: ISO
original_reference_id: GO_REF:0000096
review:
summary: positive regulation of catalytic activity is a broad ancestor for the Cdc42 signaling
role.
action: MODIFY
reason: Cdc42 is best represented as a small GTPase/Rho-family signaling switch.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: CDC42 belongs to the **Rho family** of small GTPases and acts as a
**molecular switch** cycling between **GTP-bound (active)** and **GDP-bound (inactive)**
states
proposed_replacement_terms:
- *id001
- term:
id: GO:0000139
label: Golgi membrane
evidence_type: ISO
original_reference_id: GO_REF:0000096
review:
summary: Golgi membrane is a supported context-specific Cdc42 output.
action: KEEP_AS_NON_CORE
reason: Cdc42 controls broad cellular architecture and developmental programs through
actin, polarity, trafficking, and kinase-effector pathways, but this term is not the
core molecular function.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: In its **GTP-bound state**, CDC42 binds effector proteins that drive
downstream cytoskeletal and polarity responses
- term:
id: GO:0002040
label: sprouting angiogenesis
evidence_type: ISO
original_reference_id: GO_REF:0000096
review:
summary: sprouting angiogenesis is a supported context-specific Cdc42 output.
action: KEEP_AS_NON_CORE
reason: Cdc42 controls broad cellular architecture and developmental programs through
actin, polarity, trafficking, and kinase-effector pathways, but this term is not the
core molecular function.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: In its **GTP-bound state**, CDC42 binds effector proteins that drive
downstream cytoskeletal and polarity responses
- term:
id: GO:0003924
label: GTPase activity
evidence_type: ISO
original_reference_id: GO_REF:0000119
review:
summary: GTPase activity is consistent with core Cdc42 GTPase, cytoskeletal, polarity,
or localization biology.
action: ACCEPT
reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane
localization, or immediate actin/polarity outputs.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: CDC42 is a **GTP-hydrolyzing enzyme** (small GTPase). Its substrate
is **GTP**, which it binds and hydrolyzes to **GDP + Pi**
- term:
id: GO:0005525
label: GTP binding
evidence_type: ISO
original_reference_id: GO_REF:0000096
review:
summary: GTP binding is consistent with core Cdc42 GTPase, cytoskeletal, polarity, or
localization biology.
action: ACCEPT
reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane
localization, or immediate actin/polarity outputs.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: CDC42 is a **GTP-hydrolyzing enzyme** (small GTPase). Its substrate
is **GTP**, which it binds and hydrolyzes to **GDP + Pi**
- term:
id: GO:0005525
label: GTP binding
evidence_type: ISO
original_reference_id: GO_REF:0000119
review:
summary: GTP binding is consistent with core Cdc42 GTPase, cytoskeletal, polarity, or
localization biology.
action: ACCEPT
reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane
localization, or immediate actin/polarity outputs.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: CDC42 is a **GTP-hydrolyzing enzyme** (small GTPase). Its substrate
is **GTP**, which it binds and hydrolyzes to **GDP + Pi**
- term:
id: GO:0005737
label: cytoplasm
evidence_type: ISO
original_reference_id: GO_REF:0000119
review:
summary: cytoplasm is consistent with core Cdc42 GTPase, cytoskeletal, polarity, or localization
biology.
action: ACCEPT
reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane
localization, or immediate actin/polarity outputs.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: CDC42 associates with the **plasma membrane/cell cortex** via a **carboxy-terminal
prenyl group**
- term:
id: GO:0005813
label: centrosome
evidence_type: ISO
original_reference_id: GO_REF:0000119
review:
summary: centrosome is consistent with core Cdc42 GTPase, cytoskeletal, polarity, or localization
biology.
action: ACCEPT
reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane
localization, or immediate actin/polarity outputs.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: CDC42 is directly linked to actin nucleation pathways through **WASP-family
nucleation-promoting factors**.
- term:
id: GO:0005886
label: plasma membrane
evidence_type: ISO
original_reference_id: GO_REF:0000096
review:
summary: plasma membrane is consistent with core Cdc42 GTPase, cytoskeletal, polarity,
or localization biology.
action: ACCEPT
reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane
localization, or immediate actin/polarity outputs.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: CDC42 associates with the **plasma membrane/cell cortex** via a **carboxy-terminal
prenyl group**
- term:
id: GO:0005886
label: plasma membrane
evidence_type: ISO
original_reference_id: GO_REF:0000119
review:
summary: plasma membrane is consistent with core Cdc42 GTPase, cytoskeletal, polarity,
or localization biology.
action: ACCEPT
reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane
localization, or immediate actin/polarity outputs.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: CDC42 associates with the **plasma membrane/cell cortex** via a **carboxy-terminal
prenyl group**
- term:
id: GO:0006911
label: phagocytosis, engulfment
evidence_type: ISO
original_reference_id: GO_REF:0000119
review:
summary: phagocytosis, engulfment is consistent with core Cdc42 GTPase, cytoskeletal,
polarity, or localization biology.
action: ACCEPT
reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane
localization, or immediate actin/polarity outputs.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: CDC42 is directly linked to actin nucleation pathways through **WASP-family
nucleation-promoting factors**.
- term:
id: GO:0007015
label: actin filament organization
evidence_type: ISO
original_reference_id: GO_REF:0000096
review:
summary: actin filament organization is consistent with core Cdc42 GTPase, cytoskeletal,
polarity, or localization biology.
action: ACCEPT
reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane
localization, or immediate actin/polarity outputs.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: CDC42 is directly linked to actin nucleation pathways through **WASP-family
nucleation-promoting factors**.
- term:
id: GO:0007015
label: actin filament organization
evidence_type: ISO
original_reference_id: GO_REF:0000119
review:
summary: actin filament organization is consistent with core Cdc42 GTPase, cytoskeletal,
polarity, or localization biology.
action: ACCEPT
reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane
localization, or immediate actin/polarity outputs.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: CDC42 is directly linked to actin nucleation pathways through **WASP-family
nucleation-promoting factors**.
- term:
id: GO:0007030
label: Golgi organization
evidence_type: ISO
original_reference_id: GO_REF:0000096
review:
summary: Golgi organization is a supported context-specific Cdc42 output.
action: KEEP_AS_NON_CORE
reason: Cdc42 controls broad cellular architecture and developmental programs through
actin, polarity, trafficking, and kinase-effector pathways, but this term is not the
core molecular function.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: In its **GTP-bound state**, CDC42 binds effector proteins that drive
downstream cytoskeletal and polarity responses
- term:
id: GO:0007229
label: integrin-mediated signaling pathway
evidence_type: ISO
original_reference_id: GO_REF:0000119
review:
summary: integrin-mediated signaling pathway is a supported context-specific Cdc42 output.
action: KEEP_AS_NON_CORE
reason: Cdc42 controls broad cellular architecture and developmental programs through
actin, polarity, trafficking, and kinase-effector pathways, but this term is not the
core molecular function.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: In its **GTP-bound state**, CDC42 binds effector proteins that drive
downstream cytoskeletal and polarity responses
- term:
id: GO:0010591
label: regulation of lamellipodium assembly
evidence_type: ISO
original_reference_id: GO_REF:0000119
review:
summary: regulation of lamellipodium assembly is consistent with core Cdc42 GTPase, cytoskeletal,
polarity, or localization biology.
action: ACCEPT
reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane
localization, or immediate actin/polarity outputs.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: CDC42 is directly linked to actin nucleation pathways through **WASP-family
nucleation-promoting factors**.
- term:
id: GO:0010592
label: positive regulation of lamellipodium assembly
evidence_type: ISO
original_reference_id: GO_REF:0000119
review:
summary: positive regulation of lamellipodium assembly is consistent with core Cdc42 GTPase,
cytoskeletal, polarity, or localization biology.
action: ACCEPT
reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane
localization, or immediate actin/polarity outputs.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: CDC42 is directly linked to actin nucleation pathways through **WASP-family
nucleation-promoting factors**.
- term:
id: GO:0016020
label: membrane
evidence_type: ISO
original_reference_id: GO_REF:0000119
review:
summary: membrane is consistent with core Cdc42 GTPase, cytoskeletal, polarity, or localization
biology.
action: ACCEPT
reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane
localization, or immediate actin/polarity outputs.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: CDC42 associates with the **plasma membrane/cell cortex** via a **carboxy-terminal
prenyl group**
- term:
id: GO:0017119
label: Golgi transport complex
evidence_type: ISO
original_reference_id: GO_REF:0000119
review:
summary: Golgi transport complex is a supported context-specific Cdc42 output.
action: KEEP_AS_NON_CORE
reason: Cdc42 controls broad cellular architecture and developmental programs through
actin, polarity, trafficking, and kinase-effector pathways, but this term is not the
core molecular function.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: In its **GTP-bound state**, CDC42 binds effector proteins that drive
downstream cytoskeletal and polarity responses
- term:
id: GO:0019901
label: protein kinase binding
evidence_type: ISO
original_reference_id: GO_REF:0000119
review:
summary: protein kinase binding is consistent with core Cdc42 GTPase, cytoskeletal, polarity,
or localization biology.
action: ACCEPT
reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane
localization, or immediate actin/polarity outputs.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: CDC42 is directly linked to actin nucleation pathways through **WASP-family
nucleation-promoting factors**.
- term:
id: GO:0030036
label: actin cytoskeleton organization
evidence_type: ISO
original_reference_id: GO_REF:0000119
review:
summary: actin cytoskeleton organization is consistent with core Cdc42 GTPase, cytoskeletal,
polarity, or localization biology.
action: ACCEPT
reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane
localization, or immediate actin/polarity outputs.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: CDC42 is directly linked to actin nucleation pathways through **WASP-family
nucleation-promoting factors**.
- term:
id: GO:0030141
label: secretory granule
evidence_type: ISO
original_reference_id: GO_REF:0000096
review:
summary: secretory granule is a supported context-specific Cdc42 output.
action: KEEP_AS_NON_CORE
reason: Cdc42 controls broad cellular architecture and developmental programs through
actin, polarity, trafficking, and kinase-effector pathways, but this term is not the
core molecular function.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: In its **GTP-bound state**, CDC42 binds effector proteins that drive
downstream cytoskeletal and polarity responses
- term:
id: GO:0030175
label: filopodium
evidence_type: ISO
original_reference_id: GO_REF:0000119
review:
summary: filopodium is consistent with core Cdc42 GTPase, cytoskeletal, polarity, or localization
biology.
action: ACCEPT
reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane
localization, or immediate actin/polarity outputs.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: CDC42 is directly linked to actin nucleation pathways through **WASP-family
nucleation-promoting factors**.
- term:
id: GO:0030307
label: positive regulation of cell growth
evidence_type: ISO
original_reference_id: GO_REF:0000119
review:
summary: positive regulation of cell growth is a supported context-specific Cdc42 output.
action: KEEP_AS_NON_CORE
reason: Cdc42 controls broad cellular architecture and developmental programs through
actin, polarity, trafficking, and kinase-effector pathways, but this term is not the
core molecular function.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: In its **GTP-bound state**, CDC42 binds effector proteins that drive
downstream cytoskeletal and polarity responses
- term:
id: GO:0030335
label: positive regulation of cell migration
evidence_type: ISO
original_reference_id: GO_REF:0000119
review:
summary: positive regulation of cell migration is a supported context-specific Cdc42 output.
action: KEEP_AS_NON_CORE
reason: Cdc42 controls broad cellular architecture and developmental programs through
actin, polarity, trafficking, and kinase-effector pathways, but this term is not the
core molecular function.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: In its **GTP-bound state**, CDC42 binds effector proteins that drive
downstream cytoskeletal and polarity responses
- term:
id: GO:0030496
label: midbody
evidence_type: ISO
original_reference_id: GO_REF:0000119
review:
summary: midbody is consistent with core Cdc42 GTPase, cytoskeletal, polarity, or localization
biology.
action: ACCEPT
reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane
localization, or immediate actin/polarity outputs.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: CDC42 is directly linked to actin nucleation pathways through **WASP-family
nucleation-promoting factors**.
- term:
id: GO:0031274
label: positive regulation of pseudopodium assembly
evidence_type: ISO
original_reference_id: GO_REF:0000119
review:
summary: positive regulation of pseudopodium assembly is consistent with core Cdc42 GTPase,
cytoskeletal, polarity, or localization biology.
action: ACCEPT
reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane
localization, or immediate actin/polarity outputs.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: CDC42 is directly linked to actin nucleation pathways through **WASP-family
nucleation-promoting factors**.
- term:
id: GO:0031333
label: negative regulation of protein-containing complex assembly
evidence_type: ISO
original_reference_id: GO_REF:0000119
review:
summary: negative regulation of protein-containing complex assembly is a supported context-specific
Cdc42 output.
action: KEEP_AS_NON_CORE
reason: Cdc42 controls broad cellular architecture and developmental programs through
actin, polarity, trafficking, and kinase-effector pathways, but this term is not the
core molecular function.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: In its **GTP-bound state**, CDC42 binds effector proteins that drive
downstream cytoskeletal and polarity responses
- term:
id: GO:0031435
label: mitogen-activated protein kinase kinase kinase binding
evidence_type: ISO
original_reference_id: GO_REF:0000096
review:
summary: mitogen-activated protein kinase kinase kinase binding is consistent with core
Cdc42 GTPase, cytoskeletal, polarity, or localization biology.
action: ACCEPT
reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane
localization, or immediate actin/polarity outputs.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: CDC42 is directly linked to actin nucleation pathways through **WASP-family
nucleation-promoting factors**.
- term:
id: GO:0031996
label: thioesterase binding
evidence_type: ISO
original_reference_id: GO_REF:0000119
review:
summary: thioesterase binding is a supported context-specific Cdc42 output.
action: KEEP_AS_NON_CORE
reason: Cdc42 controls broad cellular architecture and developmental programs through
actin, polarity, trafficking, and kinase-effector pathways, but this term is not the
core molecular function.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: In its **GTP-bound state**, CDC42 binds effector proteins that drive
downstream cytoskeletal and polarity responses
- term:
id: GO:0032427
label: GBD domain binding
evidence_type: ISO
original_reference_id: GO_REF:0000119
review:
summary: GBD domain binding is consistent with core Cdc42 GTPase, cytoskeletal, polarity,
or localization biology.
action: ACCEPT
reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane
localization, or immediate actin/polarity outputs.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: CDC42 is directly linked to actin nucleation pathways through **WASP-family
nucleation-promoting factors**.
- term:
id: GO:0032467
label: positive regulation of cytokinesis
evidence_type: ISO
original_reference_id: GO_REF:0000119
review:
summary: positive regulation of cytokinesis is supported for Cdc42, but this is a cell-cycle
output rather than the small GTPase catalytic role itself.
action: ACCEPT
reason: UniProt carries this transferred process annotation, but it is treated as a
downstream cell-cycle output rather than core GTPase catalysis.
supported_by:
- reference_id: UniProt:P60766
supporting_text: 'GO; GO:0032467; P:positive regulation of cytokinesis; ISS:UniProtKB.'
- term:
id: GO:0032956
label: regulation of actin cytoskeleton organization
evidence_type: ISO
original_reference_id: GO_REF:0000119
review:
summary: regulation of actin cytoskeleton organization is a supported context-specific
Cdc42 output.
action: KEEP_AS_NON_CORE
reason: Cdc42 controls broad cellular architecture and developmental programs through
actin, polarity, trafficking, and kinase-effector pathways, but this term is not the
core molecular function.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: In its **GTP-bound state**, CDC42 binds effector proteins that drive
downstream cytoskeletal and polarity responses
- term:
id: GO:0032991
label: protein-containing complex
evidence_type: ISO
original_reference_id: GO_REF:0000119
review:
summary: protein-containing complex is a supported context-specific Cdc42 output.
action: KEEP_AS_NON_CORE
reason: Cdc42 controls broad cellular architecture and developmental programs through
actin, polarity, trafficking, and kinase-effector pathways, but this term is not the
core molecular function.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: In its **GTP-bound state**, CDC42 binds effector proteins that drive
downstream cytoskeletal and polarity responses
- term:
id: GO:0034191
label: apolipoprotein A-I receptor binding
evidence_type: ISO
original_reference_id: GO_REF:0000119
review:
summary: apolipoprotein A-I receptor binding is a supported context-specific Cdc42 output.
action: KEEP_AS_NON_CORE
reason: Cdc42 controls broad cellular architecture and developmental programs through
actin, polarity, trafficking, and kinase-effector pathways, but this term is not the
core molecular function.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: In its **GTP-bound state**, CDC42 binds effector proteins that drive
downstream cytoskeletal and polarity responses
- term:
id: GO:0034329
label: cell junction assembly
evidence_type: ISO
original_reference_id: GO_REF:0000119
review:
summary: cell junction assembly is a supported context-specific Cdc42 output.
action: KEEP_AS_NON_CORE
reason: Cdc42 controls broad cellular architecture and developmental programs through
actin, polarity, trafficking, and kinase-effector pathways, but this term is not the
core molecular function.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: In its **GTP-bound state**, CDC42 binds effector proteins that drive
downstream cytoskeletal and polarity responses
- term:
id: GO:0036464
label: cytoplasmic ribonucleoprotein granule
evidence_type: ISO
original_reference_id: GO_REF:0000119
review:
summary: cytoplasmic ribonucleoprotein granule is retained as a non-core Cdc42-associated
annotation.
action: KEEP_AS_NON_CORE
reason: The annotation is plausible as a downstream or compartment-specific consequence
of Cdc42 signaling rather than the core GTPase switch activity.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: In its **GTP-bound state**, CDC42 binds effector proteins that drive
downstream cytoskeletal and polarity responses
- term:
id: GO:0038189
label: neuropilin signaling pathway
evidence_type: ISO
original_reference_id: GO_REF:0000119
review:
summary: neuropilin signaling pathway is a supported context-specific Cdc42 output.
action: KEEP_AS_NON_CORE
reason: Cdc42 controls broad cellular architecture and developmental programs through
actin, polarity, trafficking, and kinase-effector pathways, but this term is not the
core molecular function.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: In its **GTP-bound state**, CDC42 binds effector proteins that drive
downstream cytoskeletal and polarity responses
- term:
id: GO:0042802
label: identical protein binding
evidence_type: ISO
original_reference_id: GO_REF:0000119
review:
summary: identical protein binding is a supported context-specific Cdc42 output.
action: KEEP_AS_NON_CORE
reason: Cdc42 controls broad cellular architecture and developmental programs through
actin, polarity, trafficking, and kinase-effector pathways, but this term is not the
core molecular function.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: In its **GTP-bound state**, CDC42 binds effector proteins that drive
downstream cytoskeletal and polarity responses
- term:
id: GO:0043005
label: neuron projection
evidence_type: ISO
original_reference_id: GO_REF:0000119
review:
summary: neuron projection is a supported context-specific Cdc42 output.
action: KEEP_AS_NON_CORE
reason: Cdc42 controls broad cellular architecture and developmental programs through
actin, polarity, trafficking, and kinase-effector pathways, but this term is not the
core molecular function.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: In its **GTP-bound state**, CDC42 binds effector proteins that drive
downstream cytoskeletal and polarity responses
- term:
id: GO:0043025
label: neuronal cell body
evidence_type: ISO
original_reference_id: GO_REF:0000119
review:
summary: neuronal cell body is a supported context-specific Cdc42 output.
action: KEEP_AS_NON_CORE
reason: Cdc42 controls broad cellular architecture and developmental programs through
actin, polarity, trafficking, and kinase-effector pathways, but this term is not the
core molecular function.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: In its **GTP-bound state**, CDC42 binds effector proteins that drive
downstream cytoskeletal and polarity responses
- term:
id: GO:0043525
label: positive regulation of neuron apoptotic process
evidence_type: ISO
original_reference_id: GO_REF:0000096
review:
summary: positive regulation of neuron apoptotic process is a supported context-specific
Cdc42 output.
action: KEEP_AS_NON_CORE
reason: Cdc42 controls broad cellular architecture and developmental programs through
actin, polarity, trafficking, and kinase-effector pathways, but this term is not the
core molecular function.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: In its **GTP-bound state**, CDC42 binds effector proteins that drive
downstream cytoskeletal and polarity responses
- term:
id: GO:0044788
label: host-mediated perturbation of viral process
evidence_type: ISO
original_reference_id: GO_REF:0000119
review:
summary: host-mediated perturbation of viral process is a supported context-specific Cdc42
output.
action: KEEP_AS_NON_CORE
reason: Cdc42 controls broad cellular architecture and developmental programs through
actin, polarity, trafficking, and kinase-effector pathways, but this term is not the
core molecular function.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: In its **GTP-bound state**, CDC42 binds effector proteins that drive
downstream cytoskeletal and polarity responses
- term:
id: GO:0045198
label: establishment of epithelial cell apical/basal polarity
evidence_type: ISO
original_reference_id: GO_REF:0000119
review:
summary: establishment of epithelial cell apical/basal polarity is consistent with core
Cdc42 GTPase, cytoskeletal, polarity, or localization biology.
action: ACCEPT
reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane
localization, or immediate actin/polarity outputs.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: CDC42 is directly linked to actin nucleation pathways through **WASP-family
nucleation-promoting factors**.
- term:
id: GO:0045740
label: positive regulation of DNA replication
evidence_type: ISO
original_reference_id: GO_REF:0000096
review:
summary: positive regulation of DNA replication is a supported context-specific Cdc42
output.
action: KEEP_AS_NON_CORE
reason: Cdc42 controls broad cellular architecture and developmental programs through
actin, polarity, trafficking, and kinase-effector pathways, but this term is not the
core molecular function.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: In its **GTP-bound state**, CDC42 binds effector proteins that drive
downstream cytoskeletal and polarity responses
- term:
id: GO:0046330
label: positive regulation of JNK cascade
evidence_type: ISO
original_reference_id: GO_REF:0000096
review:
summary: The current local evidence supports context-specific Cdc42/p38 MAPK signaling,
but does not establish a specific JNK cascade annotation.
action: UNDECIDED
reason: Retaining this JNK-specific automated transfer requires direct term-specific evidence.
- term:
id: GO:0051233
label: spindle midzone
evidence_type: ISO
original_reference_id: GO_REF:0000119
review:
summary: spindle midzone is consistent with core Cdc42 GTPase, cytoskeletal, polarity,
or localization biology.
action: ACCEPT
reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane
localization, or immediate actin/polarity outputs.
supported_by:
- reference_id: UniProt:P60766
supporting_text: Moves to the central spindle as cells progressed through anaphase to telophase.
- term:
id: GO:0051489
label: regulation of filopodium assembly
evidence_type: ISO
original_reference_id: GO_REF:0000119
review:
summary: regulation of filopodium assembly is consistent with core Cdc42 GTPase, cytoskeletal,
polarity, or localization biology.
action: ACCEPT
reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane
localization, or immediate actin/polarity outputs.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: CDC42 is directly linked to actin nucleation pathways through **WASP-family
nucleation-promoting factors**.
- term:
id: GO:0051491
label: positive regulation of filopodium assembly
evidence_type: ISO
original_reference_id: GO_REF:0000119
review:
summary: positive regulation of filopodium assembly is consistent with core Cdc42 GTPase,
cytoskeletal, polarity, or localization biology.
action: ACCEPT
reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane
localization, or immediate actin/polarity outputs.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: CDC42 is directly linked to actin nucleation pathways through **WASP-family
nucleation-promoting factors**.
- term:
id: GO:0051492
label: regulation of stress fiber assembly
evidence_type: ISO
original_reference_id: GO_REF:0000119
review:
summary: The stress-fiber wording is too specific for the available Cdc42 evidence; the
supported biology is broader actin organization through Cdc42 effector pathways.
action: MODIFY
reason: Use a broader actin-organization term rather than treating stress-fiber assembly
as a core Cdc42 output.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: CDC42 is directly linked to actin nucleation pathways through **WASP-family
nucleation-promoting factors**.
proposed_replacement_terms:
- id: GO:0007015
label: actin filament organization
- term:
id: GO:0051496
label: positive regulation of stress fiber assembly
evidence_type: ISO
original_reference_id: GO_REF:0000119
review:
summary: The stress-fiber wording is too specific for the available Cdc42 evidence; the
supported biology is broader actin organization through Cdc42 effector pathways.
action: MODIFY
reason: Use a broader actin-organization term rather than treating stress-fiber assembly
as a core Cdc42 output.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: CDC42 is directly linked to actin nucleation pathways through **WASP-family
nucleation-promoting factors**.
proposed_replacement_terms:
- id: GO:0007015
label: actin filament organization
- term:
id: GO:0051683
label: establishment of Golgi localization
evidence_type: ISO
original_reference_id: GO_REF:0000096
review:
summary: establishment of Golgi localization is a supported context-specific Cdc42 output.
action: KEEP_AS_NON_CORE
reason: Cdc42 controls broad cellular architecture and developmental programs through
actin, polarity, trafficking, and kinase-effector pathways, but this term is not the
core molecular function.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: In its **GTP-bound state**, CDC42 binds effector proteins that drive
downstream cytoskeletal and polarity responses
- term:
id: GO:0051835
label: positive regulation of synapse structural plasticity
evidence_type: ISO
original_reference_id: GO_REF:0000096
review:
summary: positive regulation of synapse structural plasticity is a supported context-specific
Cdc42 output.
action: KEEP_AS_NON_CORE
reason: Cdc42 controls broad cellular architecture and developmental programs through
actin, polarity, trafficking, and kinase-effector pathways, but this term is not the
core molecular function.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: In its **GTP-bound state**, CDC42 binds effector proteins that drive
downstream cytoskeletal and polarity responses
- term:
id: GO:0051988
label: regulation of attachment of spindle microtubules to kinetochore
evidence_type: ISO
original_reference_id: GO_REF:0000119
review:
summary: regulation of attachment of spindle microtubules to kinetochore is consistent
with core Cdc42 GTPase, cytoskeletal, polarity, or localization biology.
action: ACCEPT
reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane
localization, or immediate actin/polarity outputs.
supported_by:
- reference_id: UniProt:P60766
supporting_text: Regulates the bipolar attachment of spindle microtubules to kinetochores
before chromosome congression in metaphase.
- term:
id: GO:0061630
label: ubiquitin protein ligase activity
evidence_type: ISO
original_reference_id: GO_REF:0000119
review:
summary: Cdc42 is a small GTPase, not a ubiquitin-protein ligase.
action: REMOVE
reason: No direct evidence supports assigning E3 ligase catalytic activity to Cdc42; this
appears to be an over-transfer from associated pathways or interactors.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: CDC42 is a **GTP-hydrolyzing enzyme** (small GTPase). Its substrate
is **GTP**, which it binds and hydrolyzes to **GDP + Pi**
- term:
id: GO:0072384
label: organelle transport along microtubule
evidence_type: ISO
original_reference_id: GO_REF:0000096
review:
summary: organelle transport along microtubule is a supported context-specific Cdc42 output.
action: KEEP_AS_NON_CORE
reason: Cdc42 controls broad cellular architecture and developmental programs through
actin, polarity, trafficking, and kinase-effector pathways, but this term is not the
core molecular function.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: In its **GTP-bound state**, CDC42 binds effector proteins that drive
downstream cytoskeletal and polarity responses
- term:
id: GO:0072686
label: mitotic spindle
evidence_type: ISO
original_reference_id: GO_REF:0000119
review:
summary: mitotic spindle is consistent with core Cdc42 GTPase, cytoskeletal, polarity,
or localization biology.
action: ACCEPT
reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane
localization, or immediate actin/polarity outputs.
supported_by:
- reference_id: UniProt:P60766
supporting_text: Cytoplasm, cytoskeleton, spindle
- term:
id: GO:0090135
label: actin filament branching
evidence_type: ISO
original_reference_id: GO_REF:0000096
review:
summary: actin filament branching is consistent with core Cdc42 GTPase, cytoskeletal,
polarity, or localization biology.
action: ACCEPT
reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane
localization, or immediate actin/polarity outputs.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: CDC42 is directly linked to actin nucleation pathways through **WASP-family
nucleation-promoting factors**.
- term:
id: GO:0090316
label: positive regulation of intracellular protein transport
evidence_type: ISO
original_reference_id: GO_REF:0000096
review:
summary: positive regulation of intracellular protein transport is a supported context-specific
Cdc42 output.
action: KEEP_AS_NON_CORE
reason: Cdc42 controls broad cellular architecture and developmental programs through
actin, polarity, trafficking, and kinase-effector pathways, but this term is not the
core molecular function.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: In its **GTP-bound state**, CDC42 binds effector proteins that drive
downstream cytoskeletal and polarity responses
- term:
id: GO:0098685
label: Schaffer collateral - CA1 synapse
evidence_type: ISO
original_reference_id: GO_REF:0000096
review:
summary: Schaffer collateral - CA1 synapse is a supported context-specific Cdc42 output.
action: KEEP_AS_NON_CORE
reason: Cdc42 controls broad cellular architecture and developmental programs through
actin, polarity, trafficking, and kinase-effector pathways, but this term is not the
core molecular function.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: In its **GTP-bound state**, CDC42 binds effector proteins that drive
downstream cytoskeletal and polarity responses
- term:
id: GO:0099159
label: regulation of modification of postsynaptic structure
evidence_type: ISO
original_reference_id: GO_REF:0000096
review:
summary: regulation of modification of postsynaptic structure is a supported context-specific
Cdc42 output.
action: KEEP_AS_NON_CORE
reason: Cdc42 controls broad cellular architecture and developmental programs through
actin, polarity, trafficking, and kinase-effector pathways, but this term is not the
core molecular function.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: In its **GTP-bound state**, CDC42 binds effector proteins that drive
downstream cytoskeletal and polarity responses
- term:
id: GO:1900026
label: positive regulation of substrate adhesion-dependent cell spreading
evidence_type: ISO
original_reference_id: GO_REF:0000119
review:
summary: positive regulation of substrate adhesion-dependent cell spreading is a supported
context-specific Cdc42 output.
action: KEEP_AS_NON_CORE
reason: Cdc42 controls broad cellular architecture and developmental programs through
actin, polarity, trafficking, and kinase-effector pathways, but this term is not the
core molecular function.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: In its **GTP-bound state**, CDC42 binds effector proteins that drive
downstream cytoskeletal and polarity responses
- term:
id: GO:0005515
label: protein binding
evidence_type: IPI
original_reference_id: PMID:24076653
review:
summary: protein binding records a physical association but is too generic to describe
the gene product function.
action: MARK_AS_OVER_ANNOTATED
reason: The evidence supports regulated signaling-complex assembly, not a meaningful standalone
protein binding function; more informative molecular and pathway terms capture the biology.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: In its **GTP-bound state**, CDC42 binds effector proteins that drive
downstream cytoskeletal and polarity responses
- term:
id: GO:0005515
label: protein binding
evidence_type: IPI
original_reference_id: PMID:37140151
review:
summary: protein binding records a physical association but is too generic to describe
the gene product function.
action: MARK_AS_OVER_ANNOTATED
reason: The evidence supports regulated signaling-complex assembly, not a meaningful standalone
protein binding function; more informative molecular and pathway terms capture the biology.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: In its **GTP-bound state**, CDC42 binds effector proteins that drive
downstream cytoskeletal and polarity responses
- term:
id: GO:0098794
label: postsynapse
evidence_type: IDA
original_reference_id: PMID:33531495
review:
summary: postsynapse is a supported context-specific Cdc42 output.
action: KEEP_AS_NON_CORE
reason: Cdc42 controls broad cellular architecture and developmental programs through
actin, polarity, trafficking, and kinase-effector pathways, but this term is not the
core molecular function.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: In its **GTP-bound state**, CDC42 binds effector proteins that drive
downstream cytoskeletal and polarity responses
- term:
id: GO:0098794
label: postsynapse
evidence_type: IMP
original_reference_id: PMID:33531495
review:
summary: postsynapse is a supported context-specific Cdc42 output.
action: KEEP_AS_NON_CORE
reason: Cdc42 controls broad cellular architecture and developmental programs through
actin, polarity, trafficking, and kinase-effector pathways, but this term is not the
core molecular function.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: In its **GTP-bound state**, CDC42 binds effector proteins that drive
downstream cytoskeletal and polarity responses
- term:
id: GO:0098978
label: glutamatergic synapse
evidence_type: IDA
original_reference_id: PMID:25851601
review:
summary: glutamatergic synapse is a supported context-specific Cdc42 output.
action: KEEP_AS_NON_CORE
reason: Cdc42 controls broad cellular architecture and developmental programs through
actin, polarity, trafficking, and kinase-effector pathways, but this term is not the
core molecular function.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: In its **GTP-bound state**, CDC42 binds effector proteins that drive
downstream cytoskeletal and polarity responses
- term:
id: GO:0098978
label: glutamatergic synapse
evidence_type: IMP
original_reference_id: PMID:25851601
review:
summary: glutamatergic synapse is a supported context-specific Cdc42 output.
action: KEEP_AS_NON_CORE
reason: Cdc42 controls broad cellular architecture and developmental programs through
actin, polarity, trafficking, and kinase-effector pathways, but this term is not the
core molecular function.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: In its **GTP-bound state**, CDC42 binds effector proteins that drive
downstream cytoskeletal and polarity responses
- term:
id: GO:0098978
label: glutamatergic synapse
evidence_type: IDA
original_reference_id: PMID:33531495
review:
summary: glutamatergic synapse is a supported context-specific Cdc42 output.
action: KEEP_AS_NON_CORE
reason: Cdc42 controls broad cellular architecture and developmental programs through
actin, polarity, trafficking, and kinase-effector pathways, but this term is not the
core molecular function.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: In its **GTP-bound state**, CDC42 binds effector proteins that drive
downstream cytoskeletal and polarity responses
- term:
id: GO:0098978
label: glutamatergic synapse
evidence_type: IMP
original_reference_id: PMID:33531495
review:
summary: glutamatergic synapse is a supported context-specific Cdc42 output.
action: KEEP_AS_NON_CORE
reason: Cdc42 controls broad cellular architecture and developmental programs through
actin, polarity, trafficking, and kinase-effector pathways, but this term is not the
core molecular function.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: In its **GTP-bound state**, CDC42 binds effector proteins that drive
downstream cytoskeletal and polarity responses
- term:
id: GO:0099175
label: regulation of postsynapse organization
evidence_type: IDA
original_reference_id: PMID:25851601
review:
summary: regulation of postsynapse organization is a supported context-specific Cdc42
output.
action: KEEP_AS_NON_CORE
reason: Cdc42 controls broad cellular architecture and developmental programs through
actin, polarity, trafficking, and kinase-effector pathways, but this term is not the
core molecular function.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: In its **GTP-bound state**, CDC42 binds effector proteins that drive
downstream cytoskeletal and polarity responses
- term:
id: GO:0099175
label: regulation of postsynapse organization
evidence_type: IMP
original_reference_id: PMID:25851601
review:
summary: regulation of postsynapse organization is a supported context-specific Cdc42
output.
action: KEEP_AS_NON_CORE
reason: Cdc42 controls broad cellular architecture and developmental programs through
actin, polarity, trafficking, and kinase-effector pathways, but this term is not the
core molecular function.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: In its **GTP-bound state**, CDC42 binds effector proteins that drive
downstream cytoskeletal and polarity responses
- term:
id: GO:0003015
label: heart process
evidence_type: IMP
original_reference_id: PMID:25197047
review:
summary: heart process is a supported context-specific Cdc42 output.
action: KEEP_AS_NON_CORE
reason: Cdc42 controls broad cellular architecture and developmental programs through
actin, polarity, trafficking, and kinase-effector pathways, but this term is not the
core molecular function.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: In its **GTP-bound state**, CDC42 binds effector proteins that drive
downstream cytoskeletal and polarity responses
- term:
id: GO:0003015
label: heart process
evidence_type: IMP
original_reference_id: PMID:31219639
review:
summary: heart process is a supported context-specific Cdc42 output.
action: KEEP_AS_NON_CORE
reason: Cdc42 controls broad cellular architecture and developmental programs through
actin, polarity, trafficking, and kinase-effector pathways, but this term is not the
core molecular function.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: In its **GTP-bound state**, CDC42 binds effector proteins that drive
downstream cytoskeletal and polarity responses
- term:
id: GO:0003253
label: cardiac neural crest cell migration involved in outflow tract morphogenesis
evidence_type: IMP
original_reference_id: PMID:31219639
review:
summary: cardiac neural crest cell migration involved in outflow tract morphogenesis is
a supported context-specific Cdc42 output.
action: KEEP_AS_NON_CORE
reason: Cdc42 controls broad cellular architecture and developmental programs through
actin, polarity, trafficking, and kinase-effector pathways, but this term is not the
core molecular function.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: In its **GTP-bound state**, CDC42 binds effector proteins that drive
downstream cytoskeletal and polarity responses
- term:
id: GO:0006468
label: protein phosphorylation
evidence_type: IMP
original_reference_id: PMID:31219639
review:
summary: Cdc42 does not itself catalyze protein phosphorylation.
action: MODIFY
reason: The evidence supports upstream small-GTPase signaling to kinase effectors such
as PAK rather than direct kinase activity by Cdc42.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: In its **GTP-bound state**, CDC42 binds effector proteins that drive
downstream cytoskeletal and polarity responses
proposed_replacement_terms:
- *id001
- term:
id: GO:0031252
label: cell leading edge
evidence_type: IDA
original_reference_id: PMID:31219639
review:
summary: cell leading edge is consistent with core Cdc42 GTPase, cytoskeletal, polarity,
or localization biology.
action: ACCEPT
reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane
localization, or immediate actin/polarity outputs.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: CDC42 is directly linked to actin nucleation pathways through **WASP-family
nucleation-promoting factors**.
- term:
id: GO:0035050
label: embryonic heart tube development
evidence_type: IMP
original_reference_id: PMID:31219639
review:
summary: embryonic heart tube development is a supported context-specific Cdc42 output.
action: KEEP_AS_NON_CORE
reason: Cdc42 controls broad cellular architecture and developmental programs through
actin, polarity, trafficking, and kinase-effector pathways, but this term is not the
core molecular function.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: In its **GTP-bound state**, CDC42 binds effector proteins that drive
downstream cytoskeletal and polarity responses
- term:
id: GO:0086100
label: endothelin receptor signaling pathway
evidence_type: IMP
original_reference_id: PMID:31219639
review:
summary: endothelin receptor signaling pathway is retained as a non-core Cdc42-associated
annotation.
action: KEEP_AS_NON_CORE
reason: The annotation is plausible as a downstream or compartment-specific consequence
of Cdc42 signaling rather than the core GTPase switch activity.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: In its **GTP-bound state**, CDC42 binds effector proteins that drive
downstream cytoskeletal and polarity responses
- term:
id: GO:0005515
label: protein binding
evidence_type: IPI
original_reference_id: PMID:15710388
review:
summary: protein binding records a physical association but is too generic to describe
the gene product function.
action: MARK_AS_OVER_ANNOTATED
reason: The evidence supports regulated signaling-complex assembly, not a meaningful standalone
protein binding function; more informative molecular and pathway terms capture the biology.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: In its **GTP-bound state**, CDC42 binds effector proteins that drive
downstream cytoskeletal and polarity responses
- term:
id: GO:0005515
label: protein binding
evidence_type: IPI
original_reference_id: PMID:18604197
review:
summary: protein binding records a physical association but is too generic to describe
the gene product function.
action: MARK_AS_OVER_ANNOTATED
reason: The evidence supports regulated signaling-complex assembly, not a meaningful standalone
protein binding function; more informative molecular and pathway terms capture the biology.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: In its **GTP-bound state**, CDC42 binds effector proteins that drive
downstream cytoskeletal and polarity responses
- term:
id: GO:0005515
label: protein binding
evidence_type: IPI
original_reference_id: PMID:21828338
review:
summary: protein binding records a physical association but is too generic to describe
the gene product function.
action: MARK_AS_OVER_ANNOTATED
reason: The evidence supports regulated signaling-complex assembly, not a meaningful standalone
protein binding function; more informative molecular and pathway terms capture the biology.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: In its **GTP-bound state**, CDC42 binds effector proteins that drive
downstream cytoskeletal and polarity responses
- term:
id: GO:0005515
label: protein binding
evidence_type: IPI
original_reference_id: PMID:8464478
review:
summary: protein binding records a physical association but is too generic to describe
the gene product function.
action: MARK_AS_OVER_ANNOTATED
reason: The evidence supports regulated signaling-complex assembly, not a meaningful standalone
protein binding function; more informative molecular and pathway terms capture the biology.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: In its **GTP-bound state**, CDC42 binds effector proteins that drive
downstream cytoskeletal and polarity responses
- term:
id: GO:0003924
label: GTPase activity
evidence_type: ISO
original_reference_id: PMID:27917469
review:
summary: GTPase activity is consistent with core Cdc42 GTPase, cytoskeletal, polarity,
or localization biology.
action: ACCEPT
reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane
localization, or immediate actin/polarity outputs.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: CDC42 is a **GTP-hydrolyzing enzyme** (small GTPase). Its substrate
is **GTP**, which it binds and hydrolyzes to **GDP + Pi**
- term:
id: GO:0048549
label: positive regulation of pinocytosis
evidence_type: IMP
original_reference_id: PMID:24792215
review:
summary: positive regulation of pinocytosis is consistent with core Cdc42 GTPase, cytoskeletal,
polarity, or localization biology.
action: ACCEPT
reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane
localization, or immediate actin/polarity outputs.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: CDC42 is directly linked to actin nucleation pathways through **WASP-family
nucleation-promoting factors**.
- term:
id: GO:0045335
label: phagocytic vesicle
evidence_type: IDA
original_reference_id: PMID:19144319
review:
summary: phagocytic vesicle is consistent with core Cdc42 GTPase, cytoskeletal, polarity,
or localization biology.
action: ACCEPT
reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane
localization, or immediate actin/polarity outputs.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: CDC42 is directly linked to actin nucleation pathways through **WASP-family
nucleation-promoting factors**.
- term:
id: GO:0071346
label: cellular response to type II interferon
evidence_type: IDA
original_reference_id: PMID:19144319
review:
summary: cellular response to type II interferon is a supported context-specific Cdc42
output.
action: KEEP_AS_NON_CORE
reason: Cdc42 controls broad cellular architecture and developmental programs through
actin, polarity, trafficking, and kinase-effector pathways, but this term is not the
core molecular function.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: In its **GTP-bound state**, CDC42 binds effector proteins that drive
downstream cytoskeletal and polarity responses
- term:
id: GO:0006911
label: phagocytosis, engulfment
evidence_type: ISS
original_reference_id: GO_REF:0000024
review:
summary: phagocytosis, engulfment is consistent with core Cdc42 GTPase, cytoskeletal,
polarity, or localization biology.
action: ACCEPT
reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane
localization, or immediate actin/polarity outputs.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: CDC42 is directly linked to actin nucleation pathways through **WASP-family
nucleation-promoting factors**.
- term:
id: GO:0007015
label: actin filament organization
evidence_type: ISS
original_reference_id: GO_REF:0000024
review:
summary: actin filament organization is consistent with core Cdc42 GTPase, cytoskeletal,
polarity, or localization biology.
action: ACCEPT
reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane
localization, or immediate actin/polarity outputs.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: CDC42 is directly linked to actin nucleation pathways through **WASP-family
nucleation-promoting factors**.
- term:
id: GO:0034329
label: cell junction assembly
evidence_type: ISS
original_reference_id: GO_REF:0000024
review:
summary: cell junction assembly is a supported context-specific Cdc42 output.
action: KEEP_AS_NON_CORE
reason: Cdc42 controls broad cellular architecture and developmental programs through
actin, polarity, trafficking, and kinase-effector pathways, but this term is not the
core molecular function.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: In its **GTP-bound state**, CDC42 binds effector proteins that drive
downstream cytoskeletal and polarity responses
- term:
id: GO:0045198
label: establishment of epithelial cell apical/basal polarity
evidence_type: ISS
original_reference_id: GO_REF:0000024
review:
summary: establishment of epithelial cell apical/basal polarity is consistent with core
Cdc42 GTPase, cytoskeletal, polarity, or localization biology.
action: ACCEPT
reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane
localization, or immediate actin/polarity outputs.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: CDC42 is directly linked to actin nucleation pathways through **WASP-family
nucleation-promoting factors**.
- term:
id: GO:0051491
label: positive regulation of filopodium assembly
evidence_type: IMP
original_reference_id: PMID:22494997
review:
summary: positive regulation of filopodium assembly is consistent with core Cdc42 GTPase,
cytoskeletal, polarity, or localization biology.
action: ACCEPT
reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane
localization, or immediate actin/polarity outputs.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: CDC42 is directly linked to actin nucleation pathways through **WASP-family
nucleation-promoting factors**.
- term:
id: GO:0060997
label: dendritic spine morphogenesis
evidence_type: IMP
original_reference_id: PMID:25851601
review:
summary: dendritic spine morphogenesis is a supported context-specific Cdc42 output.
action: KEEP_AS_NON_CORE
reason: Cdc42 controls broad cellular architecture and developmental programs through
actin, polarity, trafficking, and kinase-effector pathways, but this term is not the
core molecular function.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: In its **GTP-bound state**, CDC42 binds effector proteins that drive
downstream cytoskeletal and polarity responses
- term:
id: GO:0003924
label: GTPase activity
evidence_type: IDA
original_reference_id: PMID:18838382
review:
summary: GTPase activity is consistent with core Cdc42 GTPase, cytoskeletal, polarity,
or localization biology.
action: ACCEPT
reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane
localization, or immediate actin/polarity outputs.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: CDC42 is a **GTP-hydrolyzing enzyme** (small GTPase). Its substrate
is **GTP**, which it binds and hydrolyzes to **GDP + Pi**
- term:
id: GO:0003924
label: GTPase activity
evidence_type: IGI
original_reference_id: PMID:18838382
review:
summary: GTPase activity is consistent with core Cdc42 GTPase, cytoskeletal, polarity,
or localization biology.
action: ACCEPT
reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane
localization, or immediate actin/polarity outputs.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: CDC42 is a **GTP-hydrolyzing enzyme** (small GTPase). Its substrate
is **GTP**, which it binds and hydrolyzes to **GDP + Pi**
- term:
id: GO:0005515
label: protein binding
evidence_type: IPI
original_reference_id: PMID:18838382
review:
summary: protein binding records a physical association but is too generic to describe
the gene product function.
action: MARK_AS_OVER_ANNOTATED
reason: The evidence supports regulated signaling-complex assembly, not a meaningful standalone
protein binding function; more informative molecular and pathway terms capture the biology.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: In its **GTP-bound state**, CDC42 binds effector proteins that drive
downstream cytoskeletal and polarity responses
- term:
id: GO:0000322
label: storage vacuole
evidence_type: IDA
original_reference_id: PMID:21828338
review:
summary: storage vacuole is a supported context-specific Cdc42 output.
action: KEEP_AS_NON_CORE
reason: Cdc42 controls broad cellular architecture and developmental programs through
actin, polarity, trafficking, and kinase-effector pathways, but this term is not the
core molecular function.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: In its **GTP-bound state**, CDC42 binds effector proteins that drive
downstream cytoskeletal and polarity responses
- term:
id: GO:0005829
label: cytosol
evidence_type: IDA
original_reference_id: PMID:21828338
review:
summary: cytosol is consistent with core Cdc42 GTPase, cytoskeletal, polarity, or localization
biology.
action: ACCEPT
reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane
localization, or immediate actin/polarity outputs.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: CDC42 associates with the **plasma membrane/cell cortex** via a **carboxy-terminal
prenyl group**
- term:
id: GO:0005886
label: plasma membrane
evidence_type: IDA
original_reference_id: PMID:21828338
review:
summary: plasma membrane is consistent with core Cdc42 GTPase, cytoskeletal, polarity,
or localization biology.
action: ACCEPT
reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane
localization, or immediate actin/polarity outputs.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: CDC42 associates with the **plasma membrane/cell cortex** via a **carboxy-terminal
prenyl group**
- term:
id: GO:0005886
label: plasma membrane
evidence_type: IDA
original_reference_id: PMID:25217619
review:
summary: plasma membrane is consistent with core Cdc42 GTPase, cytoskeletal, polarity,
or localization biology.
action: ACCEPT
reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane
localization, or immediate actin/polarity outputs.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: CDC42 associates with the **plasma membrane/cell cortex** via a **carboxy-terminal
prenyl group**
- term:
id: GO:0005886
label: plasma membrane
evidence_type: TAS
original_reference_id: Reactome:R-MMU-3928643
review:
summary: plasma membrane is consistent with core Cdc42 GTPase, cytoskeletal, polarity,
or localization biology.
action: ACCEPT
reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane
localization, or immediate actin/polarity outputs.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: CDC42 associates with the **plasma membrane/cell cortex** via a **carboxy-terminal
prenyl group**
- term:
id: GO:0005886
label: plasma membrane
evidence_type: TAS
original_reference_id: Reactome:R-MMU-442572
review:
summary: plasma membrane is consistent with core Cdc42 GTPase, cytoskeletal, polarity,
or localization biology.
action: ACCEPT
reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane
localization, or immediate actin/polarity outputs.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: CDC42 associates with the **plasma membrane/cell cortex** via a **carboxy-terminal
prenyl group**
- term:
id: GO:0005886
label: plasma membrane
evidence_type: TAS
original_reference_id: Reactome:R-MMU-448947
review:
summary: plasma membrane is consistent with core Cdc42 GTPase, cytoskeletal, polarity,
or localization biology.
action: ACCEPT
reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane
localization, or immediate actin/polarity outputs.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: CDC42 associates with the **plasma membrane/cell cortex** via a **carboxy-terminal
prenyl group**
- term:
id: GO:0005886
label: plasma membrane
evidence_type: TAS
original_reference_id: Reactome:R-MMU-5665684
review:
summary: plasma membrane is consistent with core Cdc42 GTPase, cytoskeletal, polarity,
or localization biology.
action: ACCEPT
reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane
localization, or immediate actin/polarity outputs.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: CDC42 associates with the **plasma membrane/cell cortex** via a **carboxy-terminal
prenyl group**
- term:
id: GO:0006897
label: endocytosis
evidence_type: IMP
original_reference_id: PMID:24792215
review:
summary: PMID:24792215 directly links Cdc42 cycling to actin-dependent fluid-phase
endocytosis.
action: KEEP_AS_NON_CORE
reason: The process is supported for Cdc42-mediated actin cycling, but it remains a
context-specific trafficking output rather than the core small-GTPase molecular function.
supported_by:
- reference_id: PMID:24792215
supporting_text: The small GTPase Cdc42 regulates sequential synthesis and break down of actin allowing fluid-phase uptake to occur
- term:
id: GO:0043209
label: myelin sheath
evidence_type: HDA
original_reference_id: PMID:17634366
review:
summary: myelin sheath is a supported context-specific Cdc42 output.
action: KEEP_AS_NON_CORE
reason: Cdc42 controls broad cellular architecture and developmental programs through
actin, polarity, trafficking, and kinase-effector pathways, but this term is not the
core molecular function.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: In its **GTP-bound state**, CDC42 binds effector proteins that drive
downstream cytoskeletal and polarity responses
- term:
id: GO:0031256
label: leading edge membrane
evidence_type: IDA
original_reference_id: PMID:22461490
review:
summary: leading edge membrane is consistent with core Cdc42 GTPase, cytoskeletal, polarity,
or localization biology.
action: ACCEPT
reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane
localization, or immediate actin/polarity outputs.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: CDC42 is directly linked to actin nucleation pathways through **WASP-family
nucleation-promoting factors**.
- term:
id: GO:0036336
label: dendritic cell migration
evidence_type: IGI
original_reference_id: PMID:22461490
review:
summary: dendritic cell migration is a supported context-specific Cdc42 output.
action: KEEP_AS_NON_CORE
reason: Cdc42 controls broad cellular architecture and developmental programs through
actin, polarity, trafficking, and kinase-effector pathways, but this term is not the
core molecular function.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: In its **GTP-bound state**, CDC42 binds effector proteins that drive
downstream cytoskeletal and polarity responses
- term:
id: GO:0005525
label: GTP binding
evidence_type: ISO
original_reference_id: PMID:23620790
review:
summary: GTP binding is consistent with core Cdc42 GTPase, cytoskeletal, polarity, or
localization biology.
action: ACCEPT
reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane
localization, or immediate actin/polarity outputs.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: CDC42 is a **GTP-hydrolyzing enzyme** (small GTPase). Its substrate
is **GTP**, which it binds and hydrolyzes to **GDP + Pi**
- term:
id: GO:0005911
label: cell-cell junction
evidence_type: IDA
original_reference_id: PMID:23793062
review:
summary: cell-cell junction is a supported context-specific Cdc42 output.
action: KEEP_AS_NON_CORE
reason: Cdc42 controls broad cellular architecture and developmental programs through
actin, polarity, trafficking, and kinase-effector pathways, but this term is not the
core molecular function.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: In its **GTP-bound state**, CDC42 binds effector proteins that drive
downstream cytoskeletal and polarity responses
- term:
id: GO:0016020
label: membrane
evidence_type: ISS
original_reference_id: GO_REF:0000024
review:
summary: membrane is consistent with core Cdc42 GTPase, cytoskeletal, polarity, or localization
biology.
action: ACCEPT
reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane
localization, or immediate actin/polarity outputs.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: CDC42 associates with the **plasma membrane/cell cortex** via a **carboxy-terminal
prenyl group**
- term:
id: GO:1900026
label: positive regulation of substrate adhesion-dependent cell spreading
evidence_type: ISS
original_reference_id: GO_REF:0000024
review:
summary: positive regulation of substrate adhesion-dependent cell spreading is a supported
context-specific Cdc42 output.
action: KEEP_AS_NON_CORE
reason: Cdc42 controls broad cellular architecture and developmental programs through
actin, polarity, trafficking, and kinase-effector pathways, but this term is not the
core molecular function.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: In its **GTP-bound state**, CDC42 binds effector proteins that drive
downstream cytoskeletal and polarity responses
- term:
id: GO:0060501
label: positive regulation of epithelial cell proliferation involved in lung morphogenesis
evidence_type: IMP
original_reference_id: PMID:23219958
review:
summary: positive regulation of epithelial cell proliferation involved in lung morphogenesis
is a supported context-specific Cdc42 output.
action: KEEP_AS_NON_CORE
reason: Cdc42 controls broad cellular architecture and developmental programs through
actin, polarity, trafficking, and kinase-effector pathways, but this term is not the
core molecular function.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: In its **GTP-bound state**, CDC42 binds effector proteins that drive
downstream cytoskeletal and polarity responses
- term:
id: GO:0005515
label: protein binding
evidence_type: IPI
original_reference_id: PMID:10954424
review:
summary: protein binding records a physical association but is too generic to describe
the gene product function.
action: MARK_AS_OVER_ANNOTATED
reason: The evidence supports regulated signaling-complex assembly, not a meaningful standalone
protein binding function; more informative molecular and pathway terms capture the biology.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: In its **GTP-bound state**, CDC42 binds effector proteins that drive
downstream cytoskeletal and polarity responses
- term:
id: GO:0005515
label: protein binding
evidence_type: IPI
original_reference_id: PMID:11035016
review:
summary: protein binding records a physical association but is too generic to describe
the gene product function.
action: MARK_AS_OVER_ANNOTATED
reason: The evidence supports regulated signaling-complex assembly, not a meaningful standalone
protein binding function; more informative molecular and pathway terms capture the biology.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: In its **GTP-bound state**, CDC42 binds effector proteins that drive
downstream cytoskeletal and polarity responses
- term:
id: GO:0003161
label: cardiac conduction system development
evidence_type: IGI
original_reference_id: PMID:21690310
review:
summary: cardiac conduction system development is a supported context-specific Cdc42 output.
action: KEEP_AS_NON_CORE
reason: Cdc42 controls broad cellular architecture and developmental programs through
actin, polarity, trafficking, and kinase-effector pathways, but this term is not the
core molecular function.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: In its **GTP-bound state**, CDC42 binds effector proteins that drive
downstream cytoskeletal and polarity responses
- term:
id: GO:0060047
label: heart contraction
evidence_type: IGI
original_reference_id: PMID:21690310
review:
summary: heart contraction is a supported context-specific Cdc42 output.
action: KEEP_AS_NON_CORE
reason: Cdc42 controls broad cellular architecture and developmental programs through
actin, polarity, trafficking, and kinase-effector pathways, but this term is not the
core molecular function.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: In its **GTP-bound state**, CDC42 binds effector proteins that drive
downstream cytoskeletal and polarity responses
- term:
id: GO:0019901
label: protein kinase binding
evidence_type: IPI
original_reference_id: PMID:21048939
review:
summary: protein kinase binding is consistent with core Cdc42 GTPase, cytoskeletal, polarity,
or localization biology.
action: ACCEPT
reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane
localization, or immediate actin/polarity outputs.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: CDC42 is directly linked to actin nucleation pathways through **WASP-family
nucleation-promoting factors**.
- term:
id: GO:0005515
label: protein binding
evidence_type: IPI
original_reference_id: PMID:17000758
review:
summary: protein binding records a physical association but is too generic to describe
the gene product function.
action: MARK_AS_OVER_ANNOTATED
reason: The evidence supports regulated signaling-complex assembly, not a meaningful standalone
protein binding function; more informative molecular and pathway terms capture the biology.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: In its **GTP-bound state**, CDC42 binds effector proteins that drive
downstream cytoskeletal and polarity responses
- term:
id: GO:0030496
label: midbody
evidence_type: ISS
original_reference_id: GO_REF:0000024
review:
summary: midbody is consistent with core Cdc42 GTPase, cytoskeletal, polarity, or localization
biology.
action: ACCEPT
reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane
localization, or immediate actin/polarity outputs.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: CDC42 is directly linked to actin nucleation pathways through **WASP-family
nucleation-promoting factors**.
- term:
id: GO:0032467
label: positive regulation of cytokinesis
evidence_type: ISS
original_reference_id: GO_REF:0000024
review:
summary: positive regulation of cytokinesis is supported for Cdc42, but this is a cell-cycle
output rather than the small GTPase catalytic role itself.
action: ACCEPT
reason: UniProt carries this transferred process annotation, but it is treated as a
downstream cell-cycle output rather than core GTPase catalysis.
supported_by:
- reference_id: UniProt:P60766
supporting_text: 'GO; GO:0032467; P:positive regulation of cytokinesis; ISS:UniProtKB.'
- term:
id: GO:0051233
label: spindle midzone
evidence_type: ISS
original_reference_id: GO_REF:0000024
review:
summary: spindle midzone is consistent with core Cdc42 GTPase, cytoskeletal, polarity,
or localization biology.
action: ACCEPT
reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane
localization, or immediate actin/polarity outputs.
supported_by:
- reference_id: UniProt:P60766
supporting_text: Moves to the central spindle as cells progressed through anaphase to telophase.
- term:
id: GO:0051489
label: regulation of filopodium assembly
evidence_type: ISS
original_reference_id: GO_REF:0000024
review:
summary: regulation of filopodium assembly is consistent with core Cdc42 GTPase, cytoskeletal,
polarity, or localization biology.
action: ACCEPT
reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane
localization, or immediate actin/polarity outputs.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: CDC42 is directly linked to actin nucleation pathways through **WASP-family
nucleation-promoting factors**.
- term:
id: GO:0051988
label: regulation of attachment of spindle microtubules to kinetochore
evidence_type: ISS
original_reference_id: GO_REF:0000024
review:
summary: regulation of attachment of spindle microtubules to kinetochore is consistent
with core Cdc42 GTPase, cytoskeletal, polarity, or localization biology.
action: ACCEPT
reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane
localization, or immediate actin/polarity outputs.
supported_by:
- reference_id: UniProt:P60766
supporting_text: Regulates the bipolar attachment of spindle microtubules to kinetochores
before chromosome congression in metaphase.
- term:
id: GO:0072686
label: mitotic spindle
evidence_type: ISS
original_reference_id: GO_REF:0000024
review:
summary: mitotic spindle is consistent with core Cdc42 GTPase, cytoskeletal, polarity,
or localization biology.
action: ACCEPT
reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane
localization, or immediate actin/polarity outputs.
supported_by:
- reference_id: UniProt:P60766
supporting_text: Cytoplasm, cytoskeleton, spindle
- term:
id: GO:0005737
label: cytoplasm
evidence_type: IDA
original_reference_id: PMID:19796622
review:
summary: cytoplasm is consistent with core Cdc42 GTPase, cytoskeletal, polarity, or localization
biology.
action: ACCEPT
reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane
localization, or immediate actin/polarity outputs.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: CDC42 associates with the **plasma membrane/cell cortex** via a **carboxy-terminal
prenyl group**
- term:
id: GO:0071944
label: cell periphery
evidence_type: IDA
original_reference_id: PMID:19796622
review:
summary: cell periphery is consistent with core Cdc42 GTPase, cytoskeletal, polarity,
or localization biology.
action: ACCEPT
reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane
localization, or immediate actin/polarity outputs.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: CDC42 associates with the **plasma membrane/cell cortex** via a **carboxy-terminal
prenyl group**
- term:
id: GO:0005737
label: cytoplasm
evidence_type: IDA
original_reference_id: PMID:15775979
review:
summary: cytoplasm is consistent with core Cdc42 GTPase, cytoskeletal, polarity, or localization
biology.
action: ACCEPT
reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane
localization, or immediate actin/polarity outputs.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: CDC42 associates with the **plasma membrane/cell cortex** via a **carboxy-terminal
prenyl group**
- term:
id: GO:0043410
label: positive regulation of MAPK cascade
evidence_type: IDA
original_reference_id: PMID:19244314
review:
summary: positive regulation of MAPK cascade is supported in a Cdo/JLP/Bnip-2 neuronal
differentiation context, but it is not Cdc42's core molecular role.
action: KEEP_AS_NON_CORE
reason: The cited evidence supports a context-specific Cdc42/p38 MAPK signaling output.
supported_by:
- reference_id: PMID:19244314
supporting_text: These molecules regulate Cdc42 and p38MAPK activities, which increase
in a Cdo-dependent manner during neuronal differentiation of C17.2 cells and retinoic
acid-treated P19 cells.
- term:
id: GO:0003924
label: GTPase activity
evidence_type: ISA
original_reference_id: PMID:12637522
review:
summary: GTPase activity is consistent with core Cdc42 GTPase, cytoskeletal, polarity,
or localization biology.
action: ACCEPT
reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane
localization, or immediate actin/polarity outputs.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: CDC42 is a **GTP-hydrolyzing enzyme** (small GTPase). Its substrate
is **GTP**, which it binds and hydrolyzes to **GDP + Pi**
- term:
id: GO:0007097
label: nuclear migration
evidence_type: IMP
original_reference_id: PMID:16892058
review:
summary: nuclear migration is a supported context-specific Cdc42 output.
action: KEEP_AS_NON_CORE
reason: Cdc42 controls broad cellular architecture and developmental programs through
actin, polarity, trafficking, and kinase-effector pathways, but this term is not the
core molecular function.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: In its **GTP-bound state**, CDC42 binds effector proteins that drive
downstream cytoskeletal and polarity responses
- term:
id: GO:0008104
label: intracellular protein localization
evidence_type: IMP
original_reference_id: PMID:16621792
review:
summary: intracellular protein localization is a supported context-specific Cdc42 output.
action: KEEP_AS_NON_CORE
reason: Cdc42 controls broad cellular architecture and developmental programs through
actin, polarity, trafficking, and kinase-effector pathways, but this term is not the
core molecular function.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: In its **GTP-bound state**, CDC42 binds effector proteins that drive
downstream cytoskeletal and polarity responses
- term:
id: GO:0034332
label: adherens junction organization
evidence_type: IMP
original_reference_id: PMID:16892058
review:
summary: adherens junction organization is a supported context-specific Cdc42 output.
action: KEEP_AS_NON_CORE
reason: Cdc42 controls broad cellular architecture and developmental programs through
actin, polarity, trafficking, and kinase-effector pathways, but this term is not the
core molecular function.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: In its **GTP-bound state**, CDC42 binds effector proteins that drive
downstream cytoskeletal and polarity responses
- term:
id: GO:0035088
label: establishment or maintenance of apical/basal cell polarity
evidence_type: IMP
original_reference_id: PMID:16892058
review:
summary: establishment or maintenance of apical/basal cell polarity is consistent with
core Cdc42 GTPase, cytoskeletal, polarity, or localization biology.
action: ACCEPT
reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane
localization, or immediate actin/polarity outputs.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: CDC42 is directly linked to actin nucleation pathways through **WASP-family
nucleation-promoting factors**.
- term:
id: GO:0051647
label: nucleus localization
evidence_type: IMP
original_reference_id: PMID:16892058
review:
summary: nucleus localization is a supported context-specific Cdc42 output.
action: KEEP_AS_NON_CORE
reason: Cdc42 controls broad cellular architecture and developmental programs through
actin, polarity, trafficking, and kinase-effector pathways, but this term is not the
core molecular function.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: In its **GTP-bound state**, CDC42 binds effector proteins that drive
downstream cytoskeletal and polarity responses
- term:
id: GO:0007088
label: regulation of mitotic nuclear division
evidence_type: IMP
original_reference_id: PMID:16892058
review:
summary: regulation of mitotic nuclear division is a supported context-specific Cdc42
output.
action: KEEP_AS_NON_CORE
reason: Cdc42 controls broad cellular architecture and developmental programs through
actin, polarity, trafficking, and kinase-effector pathways, but this term is not the
core molecular function.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: In its **GTP-bound state**, CDC42 binds effector proteins that drive
downstream cytoskeletal and polarity responses
- term:
id: GO:0045177
label: apical part of cell
evidence_type: IDA
original_reference_id: PMID:16892058
review:
summary: apical part of cell is a supported context-specific Cdc42 output.
action: KEEP_AS_NON_CORE
reason: Cdc42 controls broad cellular architecture and developmental programs through
actin, polarity, trafficking, and kinase-effector pathways, but this term is not the
core molecular function.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: In its **GTP-bound state**, CDC42 binds effector proteins that drive
downstream cytoskeletal and polarity responses
- term:
id: GO:0048664
label: neuron fate determination
evidence_type: IMP
original_reference_id: PMID:16892058
review:
summary: neuron fate determination is a supported context-specific Cdc42 output.
action: KEEP_AS_NON_CORE
reason: Cdc42 controls broad cellular architecture and developmental programs through
actin, polarity, trafficking, and kinase-effector pathways, but this term is not the
core molecular function.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: In its **GTP-bound state**, CDC42 binds effector proteins that drive
downstream cytoskeletal and polarity responses
- term:
id: GO:0007163
label: establishment or maintenance of cell polarity
evidence_type: TAS
original_reference_id: PMID:10954424
review:
summary: establishment or maintenance of cell polarity is consistent with core Cdc42 GTPase,
cytoskeletal, polarity, or localization biology.
action: ACCEPT
reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane
localization, or immediate actin/polarity outputs.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: CDC42 is directly linked to actin nucleation pathways through **WASP-family
nucleation-promoting factors**.
- term:
id: GO:0016197
label: endosomal transport
evidence_type: TAS
original_reference_id: PMID:10954424
review:
summary: endosomal transport is a supported context-specific Cdc42 output.
action: KEEP_AS_NON_CORE
reason: Cdc42 controls broad cellular architecture and developmental programs through
actin, polarity, trafficking, and kinase-effector pathways, but this term is not the
core molecular function.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: In its **GTP-bound state**, CDC42 binds effector proteins that drive
downstream cytoskeletal and polarity responses
- term:
id: GO:0098609
label: cell-cell adhesion
evidence_type: TAS
original_reference_id: PMID:10954424
review:
summary: cell-cell adhesion is a supported context-specific Cdc42 output.
action: KEEP_AS_NON_CORE
reason: Cdc42 controls broad cellular architecture and developmental programs through
actin, polarity, trafficking, and kinase-effector pathways, but this term is not the
core molecular function.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: In its **GTP-bound state**, CDC42 binds effector proteins that drive
downstream cytoskeletal and polarity responses
- term:
id: GO:0007097
label: nuclear migration
evidence_type: IMP
original_reference_id: PMID:15882626
review:
summary: nuclear migration is a supported context-specific Cdc42 output.
action: KEEP_AS_NON_CORE
reason: Cdc42 controls broad cellular architecture and developmental programs through
actin, polarity, trafficking, and kinase-effector pathways, but this term is not the
core molecular function.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: In its **GTP-bound state**, CDC42 binds effector proteins that drive
downstream cytoskeletal and polarity responses
- term:
id: GO:0005515
label: protein binding
evidence_type: IPI
original_reference_id: PMID:15996550
review:
summary: protein binding records a physical association but is too generic to describe
the gene product function.
action: MARK_AS_OVER_ANNOTATED
reason: The evidence supports regulated signaling-complex assembly, not a meaningful standalone
protein binding function; more informative molecular and pathway terms capture the biology.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: In its **GTP-bound state**, CDC42 binds effector proteins that drive
downstream cytoskeletal and polarity responses
- term:
id: GO:0042995
label: cell projection
evidence_type: IDA
original_reference_id: PMID:15728722
review:
summary: cell projection is a supported context-specific Cdc42 output.
action: KEEP_AS_NON_CORE
reason: Cdc42 controls broad cellular architecture and developmental programs through
actin, polarity, trafficking, and kinase-effector pathways, but this term is not the
core molecular function.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: In its **GTP-bound state**, CDC42 binds effector proteins that drive
downstream cytoskeletal and polarity responses
- term:
id: GO:0051897
label: positive regulation of phosphatidylinositol 3-kinase/protein kinase B signal transduction
evidence_type: IMP
original_reference_id: PMID:15728722
review:
summary: positive regulation of phosphatidylinositol 3-kinase/protein kinase B signal
transduction is a supported context-specific Cdc42 output.
action: KEEP_AS_NON_CORE
reason: Cdc42 controls broad cellular architecture and developmental programs through
actin, polarity, trafficking, and kinase-effector pathways, but this term is not the
core molecular function.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: In its **GTP-bound state**, CDC42 binds effector proteins that drive
downstream cytoskeletal and polarity responses
- term:
id: GO:0005515
label: protein binding
evidence_type: IPI
original_reference_id: PMID:16052498
review:
summary: protein binding records a physical association but is too generic to describe
the gene product function.
action: MARK_AS_OVER_ANNOTATED
reason: The evidence supports regulated signaling-complex assembly, not a meaningful standalone
protein binding function; more informative molecular and pathway terms capture the biology.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: In its **GTP-bound state**, CDC42 binds effector proteins that drive
downstream cytoskeletal and polarity responses
- term:
id: GO:0005515
label: protein binding
evidence_type: IPI
original_reference_id: PMID:12773384
review:
summary: protein binding records a physical association but is too generic to describe
the gene product function.
action: MARK_AS_OVER_ANNOTATED
reason: The evidence supports regulated signaling-complex assembly, not a meaningful standalone
protein binding function; more informative molecular and pathway terms capture the biology.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: In its **GTP-bound state**, CDC42 binds effector proteins that drive
downstream cytoskeletal and polarity responses
- term:
id: GO:0003924
label: GTPase activity
evidence_type: IDA
original_reference_id: PMID:15249579
review:
summary: GTPase activity is consistent with core Cdc42 GTPase, cytoskeletal, polarity,
or localization biology.
action: ACCEPT
reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane
localization, or immediate actin/polarity outputs.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: CDC42 is a **GTP-hydrolyzing enzyme** (small GTPase). Its substrate
is **GTP**, which it binds and hydrolyzes to **GDP + Pi**
- term:
id: GO:0030742
label: GTP-dependent protein binding
evidence_type: IPI
original_reference_id: PMID:10954424
review:
summary: GTP-dependent protein binding is consistent with core Cdc42 GTPase, cytoskeletal,
polarity, or localization biology.
action: ACCEPT
reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane
localization, or immediate actin/polarity outputs.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: CDC42 is directly linked to actin nucleation pathways through **WASP-family
nucleation-promoting factors**.
- term:
id: GO:0003924
label: GTPase activity
evidence_type: IDA
original_reference_id: PMID:10699171
review:
summary: GTPase activity is consistent with core Cdc42 GTPase, cytoskeletal, polarity,
or localization biology.
action: ACCEPT
reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane
localization, or immediate actin/polarity outputs.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: CDC42 is a **GTP-hydrolyzing enzyme** (small GTPase). Its substrate
is **GTP**, which it binds and hydrolyzes to **GDP + Pi**
- term:
id: GO:0046847
label: filopodium assembly
evidence_type: IDA
original_reference_id: PMID:10699171
review:
summary: filopodium assembly is consistent with core Cdc42 GTPase, cytoskeletal, polarity,
or localization biology.
action: ACCEPT
reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane
localization, or immediate actin/polarity outputs.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: CDC42 is directly linked to actin nucleation pathways through **WASP-family
nucleation-promoting factors**.
- term:
id: GO:0003924
label: GTPase activity
evidence_type: TAS
original_reference_id: PMID:10490598
review:
summary: GTPase activity is consistent with core Cdc42 GTPase, cytoskeletal, polarity,
or localization biology.
action: ACCEPT
reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane
localization, or immediate actin/polarity outputs.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: CDC42 is a **GTP-hydrolyzing enzyme** (small GTPase). Its substrate
is **GTP**, which it binds and hydrolyzes to **GDP + Pi**
- term:
id: GO:0007266
label: Rho protein signal transduction
evidence_type: TAS
original_reference_id: PMID:10490598
review:
summary: Rho protein signal transduction is consistent with core Cdc42 GTPase, cytoskeletal,
polarity, or localization biology.
action: ACCEPT
reason: The term directly reflects Cdc42 GDP/GTP switch activity, effector binding, membrane
localization, or immediate actin/polarity outputs.
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: CDC42 is directly linked to actin nucleation pathways through **WASP-family
nucleation-promoting factors**.
core_functions:
- description: Cycles between GDP- and GTP-bound states and hydrolyzes GTP to act as a Rho-family
molecular switch.
molecular_function: *id002
directly_involved_in:
- id: GO:0007266
label: Rho protein signal transduction
locations:
- id: GO:0005886
label: plasma membrane
- id: GO:0005829
label: cytosol
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: CDC42 is a **GTP-hydrolyzing enzyme** (small GTPase). Its substrate is
**GTP**, which it binds and hydrolyzes to **GDP + Pi**
- description: Recruits active-state effectors including WASP/N-WASP, PAK, and polarity complexes
to organize actin, filopodia, cell polarity, and migration.
molecular_function:
id: GO:0030742
label: GTP-dependent protein binding
directly_involved_in:
- id: GO:0007015
label: actin filament organization
- id: GO:0030010
label: establishment of cell polarity
- id: GO:0046847
label: filopodium assembly
locations:
- id: GO:0005886
label: plasma membrane
- id: GO:0031256
label: leading edge membrane
supported_by:
- reference_id: file:mouse/Cdc42/Cdc42-deep-research-falcon.md
supporting_text: CDC42 is directly linked to actin nucleation pathways through **WASP-family
nucleation-promoting factors**.
proposed_new_terms: []
suggested_questions:
- question: Which mouse Cdc42 annotations should be isoform-qualified for prenylated versus
palmitoylated Cdc42 products?
- question: Which neuronal/synaptic Cdc42 terms are directly supported for the brain-enriched
isoform rather than inferred from general Rho-family biology?
suggested_experiments:
- description: Use isoform-specific knock-in tags and rescue alleles to measure Cdc42 effector
recruitment at leading edge, Golgi/endosomal, midbody, and neuronal compartments.
hypothesis: Cdc42 pleiotropy is primarily explained by isoform- and lipidation-dependent
localization rather than different intrinsic GTPase biochemistry.
experiment_type: Live-cell imaging and isoform-specific rescue