GO_REF:0000002
Gene Ontology annotation through association of InterPro records with GO terms
GO_REF:0000024
Manual transfer of experimentally-verified manual GO annotation data to orthologs by curator judgment of sequence similarity
GO_REF:0000033
Annotation inferences using phylogenetic trees
GO_REF:0000044
Gene Ontology annotation based on UniProtKB/Swiss-Prot Subcellular Location vocabulary mapping, accompanied by conservative changes to GO terms applied by UniProt
GO_REF:0000107
Automatic transfer of experimentally verified manual GO annotation data to orthologs using Ensembl Compara
GO_REF:0000108
Automatic assignment of GO terms using logical inference, based on on inter-ontology links
GO_REF:0000116
Automatic Gene Ontology annotation based on Rhea mapping
GO_REF:0000117
Electronic Gene Ontology annotations created by ARBA machine learning models
GO_REF:0000120
Combined Automated Annotation using Multiple IEA Methods
PMID:10764818
The isolation and characterization of a cDNA encoding phospholipid-specific inositol polyphosphate 5-phosphatase.
PMID:19668215
INPP5E mutations cause primary cilium signaling defects, ciliary instability and ciliopathies in human and mouse.
PMID:19668216
Mutations in INPP5E, encoding inositol polyphosphate-5-phosphatase E, link phosphatidyl inositol signaling to the ciliopathies.
PMID:28514442
Architecture of the human interactome defines protein communities and disease networks.
PMID:33961781
Dual proteome-scale networks reveal cell-specific remodeling of the human interactome.
PMID:35271311
OpenCell: Endogenous tagging for the cartography of human cellular organization.
PMID:36931259
A central chaperone-like role for 14-3-3 proteins in human cells.
Reactome:R-HSA-1660514
Synthesis of PIPs at the Golgi membrane
Reactome:R-HSA-1675824
PI(4,5)P2 is dephosphorylated to PI4P by OCRL/INPP5E at the Golgi membrane
Reactome:R-HSA-5624953
ARL13B binds INPP5E
Reactome:R-HSA-5624954
INPP5E translocates to the primary cilium
Reactome:R-HSA-5624956
PDE6D binds INPP5E
Reactome:R-HSA-5638012
PDE6D dissociates from ARL13B:INPP5E
PMID:24166846
A homozygous PDE6D mutation in Joubert syndrome impairs targeting of farnesylated INPP5E protein to the primary cilium.
PMID:26190144
Modulation of Ciliary Phosphoinositide Content Regulates Trafficking and Sonic Hedgehog Signaling Output.
PMID:26305592
Phosphoinositides Regulate Ciliary Protein Trafficking to Modulate Hedgehog Signaling.
file:human/INPP5E/INPP5E-deep-research-falcon.md
INPP5E-deep-research-falcon.md
file:human/INPP5E/INPP5E-uniprot.txt
UniProtKB Q9NRR6 (INPP5E) entry
PMID:21436142
Regulation of IGF-1/PI3K/Akt signalling by the phosphoinositide phosphatase pharbin.