Chrna9

UniProt ID: P43144
Organism: Rattus norvegicus
Review Status: COMPLETE
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Gene Description

Chrna9 encodes the alpha9 subunit of an acetylcholine-gated cation channel associated with efferent signaling to inner-ear hair cells. Rat alpha9 can form functional homomers in oocytes, but the native auditory receptor includes alpha10. Calcium entry through the receptor recruits calcium-dependent potassium channels, allowing a cation channel to mediate net inhibition of hair cells. Rat alpha9/alpha10 receptors have high relative calcium permeability compared with chicken; choline is a partial agonist in rat. Nicotine antagonizes the ordinary alpha9/alpha10 channel rather than serving as its canonical activating agonist.

Existing Annotations Review

GO Term Evidence Action Reason
GO:0004888 transmembrane signaling receptor activity
IEA
GO_REF:0000002
MODIFY
Summary: Rat alpha9/alpha10 receptor assays resolve the channel to acetylcholine-gated cation transport.
Reason: The subunit supplies part of the pentameric pore and gating machinery; it is not being treated as a complete isolated channel. Refine to the existing specific MF. The original IEA assertion (GO_REF:0000002) is retained in the payload; this assessment uses independent receptor measurements rather than a GO annotation as evidence.
Supporting Evidence:
GO:0005216 monoatomic ion channel activity
IEA
GO_REF:0000002
MODIFY
Summary: Rat alpha9/alpha10 receptor assays resolve the channel to acetylcholine-gated cation transport.
Reason: The subunit supplies part of the pentameric pore and gating machinery; it is not being treated as a complete isolated channel. Refine to the existing specific MF. The original IEA assertion (GO_REF:0000002) is retained in the payload; this assessment uses independent receptor measurements rather than a GO annotation as evidence.
Supporting Evidence:
GO:0005230 extracellular ligand-gated monoatomic ion channel activity
IEA
GO_REF:0000002
MODIFY
Summary: Rat alpha9/alpha10 receptor assays resolve the channel to acetylcholine-gated cation transport.
Reason: The subunit supplies part of the pentameric pore and gating machinery; it is not being treated as a complete isolated channel. Refine to the existing specific MF. The original IEA assertion (GO_REF:0000002) is retained in the payload; this assessment uses independent receptor measurements rather than a GO annotation as evidence.
Supporting Evidence:
GO:0005886 plasma membrane
EXP
PMID:10713500
High calcium permeability and calcium block of the alpha9 ni...
ACCEPT
Summary: Recombinant currents demonstrate functional surface channels; native hair-cell experiments establish the physiological membrane pool.
Reason: Rat recombinant/native comparisons are used at their stated species and assay scope. The original EXP assertion (PMID:10713500) is retained in the payload; this assessment uses independent receptor measurements rather than a GO annotation as evidence.
GO:0005886 plasma membrane
EXP
PMID:11248107
alpha10: a determinant of nicotinic cholinergic receptor fun...
ACCEPT
Summary: Recombinant currents demonstrate functional surface channels; native hair-cell experiments establish the physiological membrane pool.
Reason: Rat recombinant/native comparisons are used at their stated species and assay scope. The original EXP assertion (PMID:11248107) is retained in the payload; this assessment uses independent receptor measurements rather than a GO annotation as evidence.
GO:0005886 plasma membrane
EXP
PMID:12117536
The alpha9alpha10 nicotinic acetylcholine receptor is permea...
ACCEPT
Summary: Recombinant currents demonstrate functional surface channels; native hair-cell experiments establish the physiological membrane pool.
Reason: Rat recombinant/native comparisons are used at their stated species and assay scope. The original EXP assertion (PMID:12117536) is retained in the payload; this assessment uses independent receptor measurements rather than a GO annotation as evidence.
GO:0005886 plasma membrane
EXP
PMID:7954834
Alpha 9: an acetylcholine receptor with novel pharmacologica...
ACCEPT
Summary: Recombinant currents demonstrate functional surface channels; native hair-cell experiments establish the physiological membrane pool.
Reason: Rat recombinant/native comparisons are used at their stated species and assay scope. The original EXP assertion (PMID:7954834) is retained in the payload; this assessment uses independent receptor measurements rather than a GO annotation as evidence.
GO:0005886 plasma membrane
IBA
GO_REF:0000033
ACCEPT
Summary: Recombinant currents demonstrate functional surface channels; native hair-cell experiments establish the physiological membrane pool.
Reason: Rat recombinant/native comparisons are used at their stated species and assay scope. The original IBA assertion (GO_REF:0000033) is retained in the payload; this assessment uses independent receptor measurements rather than a GO annotation as evidence.
GO:0005886 plasma membrane
IEA
GO_REF:0000120
ACCEPT
Summary: Recombinant currents demonstrate functional surface channels; native hair-cell experiments establish the physiological membrane pool.
Reason: Rat recombinant/native comparisons are used at their stated species and assay scope. The original IEA assertion (GO_REF:0000120) is retained in the payload; this assessment uses independent receptor measurements rather than a GO annotation as evidence.
GO:0005886 plasma membrane
ISO
GO_REF:0000121
ACCEPT
Summary: Recombinant currents demonstrate functional surface channels; native hair-cell experiments establish the physiological membrane pool.
Reason: Rat recombinant/native comparisons are used at their stated species and assay scope. The original ISO assertion (GO_REF:0000121) is retained in the payload; this assessment uses independent receptor measurements rather than a GO annotation as evidence.
GO:0005886 plasma membrane
TAS
Reactome:R-RNO-9667850
ACCEPT
Summary: Recombinant currents demonstrate functional surface channels; native hair-cell experiments establish the physiological membrane pool.
Reason: Rat recombinant/native comparisons are used at their stated species and assay scope. The original TAS assertion (Reactome:R-RNO-9667850) is retained in the payload; this assessment uses independent receptor measurements rather than a GO annotation as evidence.
GO:0005886 plasma membrane
TAS
Reactome:R-RNO-9667857
ACCEPT
Summary: Recombinant currents demonstrate functional surface channels; native hair-cell experiments establish the physiological membrane pool.
Reason: Rat recombinant/native comparisons are used at their stated species and assay scope. The original TAS assertion (Reactome:R-RNO-9667857) is retained in the payload; this assessment uses independent receptor measurements rather than a GO annotation as evidence.
GO:0005892 acetylcholine-gated channel complex
IDA
PMID:12401316
Coexpression of alpha 9 and alpha 10 nicotinic acetylcholine...
ACCEPT
Summary: Coexpressed alpha9 and alpha10 form functional acetylcholine-gated receptor complexes.
Reason: Rat recombinant/native comparisons are used at their stated species and assay scope. The original IDA assertion (PMID:12401316) is retained in the payload; this assessment uses independent receptor measurements rather than a GO annotation as evidence.
GO:0005892 acetylcholine-gated channel complex
IEA
GO_REF:0000120
ACCEPT
Summary: Coexpressed alpha9 and alpha10 form functional acetylcholine-gated receptor complexes.
Reason: Rat recombinant/native comparisons are used at their stated species and assay scope. The original IEA assertion (GO_REF:0000120) is retained in the payload; this assessment uses independent receptor measurements rather than a GO annotation as evidence.
GO:0005892 acetylcholine-gated channel complex
ISO
GO_REF:0000121
ACCEPT
Summary: Coexpressed alpha9 and alpha10 form functional acetylcholine-gated receptor complexes.
Reason: Rat recombinant/native comparisons are used at their stated species and assay scope. The original ISO assertion (GO_REF:0000121) is retained in the payload; this assessment uses independent receptor measurements rather than a GO annotation as evidence.
GO:0006811 monoatomic ion transport
IEA
GO_REF:0000002
MODIFY
Summary: The measured receptor conducts cations across the membrane, including calcium.
Reason: Refine the broad transport term to cation transmembrane transport, preserving monovalent and divalent flux rather than narrowing the entire current to calcium. The original IEA assertion (GO_REF:0000002) is retained in the payload; this assessment uses independent receptor measurements rather than a GO annotation as evidence.
Supporting Evidence:
GO:0006812 monoatomic cation transport
ISO
GO_REF:0000121
MODIFY
Summary: The measured receptor conducts cations across the membrane, including calcium.
Reason: Refine the broad transport term to cation transmembrane transport, preserving monovalent and divalent flux rather than narrowing the entire current to calcium. The original ISO assertion (GO_REF:0000121) is retained in the payload; this assessment uses independent receptor measurements rather than a GO annotation as evidence.
Propagation Review
Root cause: NO FAILURE CORE
Sources checked:
MGI:MGI:1202403 SUPPORTS TRANSFER
The measured receptor conducts cations across the membrane, including calcium. Refine the broad transport term to cation transmembrane transport, preserving monovalent and divalent flux rather than narrowing the entire current to calcium. The original ISO assertion (GO_REF:0000121) is retained in the payload; this assessment uses independent receptor measurements rather than a GO annotation as evidence.
Supporting Evidence:
GO:0006816 calcium ion transport
IBA
GO_REF:0000033
ACCEPT
Summary: Alpha9/alpha10 channels conduct calcium; direct rat measurements and the human functional study support the conserved subunit contribution.
Reason: This term states calcium transport, not calcium exclusivity or identical permeability across species.
GO:0007204 positive regulation of cytosolic calcium ion concentration
ISO
GO_REF:0000121
ACCEPT
Summary: Receptor-mediated calcium entry increases cytosolic calcium and recruits downstream conductances; it is not simply calcium release from stores.
Reason: Rat recombinant/native comparisons are used at their stated species and assay scope. The original ISO assertion (GO_REF:0000121) is retained in the payload; this assessment uses independent receptor measurements rather than a GO annotation as evidence.
GO:0007271 synaptic transmission, cholinergic
IBA
GO_REF:0000033
ACCEPT
Summary: The receptor performs the postsynaptic receiver step of efferent cholinergic transmission.
Reason: Rat recombinant/native comparisons are used at their stated species and assay scope. The original IBA assertion (GO_REF:0000033) is retained in the payload; this assessment uses independent receptor measurements rather than a GO annotation as evidence.
GO:0010996 response to auditory stimulus
IEA
GO_REF:0000107
KEEP AS NON CORE
Summary: Native auditory experiments and alpha9/alpha10 knockout studies establish efferent modulation of cochlear responses.
Reason: Retain a role in auditory response at that resolution, without calling the receptor a mechanically gated sound sensor or inferring all mammalian perceptual phenotypes in this species.
GO:0010996 response to auditory stimulus
ISO
GO_REF:0000121
KEEP AS NON CORE
Summary: Native auditory experiments and alpha9/alpha10 knockout studies establish efferent modulation of cochlear responses.
Reason: Retain a role in auditory response at that resolution, without calling the receptor a mechanically gated sound sensor or inferring all mammalian perceptual phenotypes in this species.
GO:0016020 membrane
IEA
GO_REF:0000002
MODIFY
Summary: The relevant auditory receptor pool is on the postsynaptic hair-cell plasma membrane.
Reason: Refine this general membrane location to the already represented postsynaptic membrane; recombinant surface currents corroborate membrane insertion but are not native localization measurements. The original IEA assertion (GO_REF:0000002) is retained in the payload; this assessment uses independent receptor measurements rather than a GO annotation as evidence.
Proposed replacements: postsynaptic membrane
Supporting Evidence:
GO:0022848 acetylcholine-gated monoatomic cation-selective channel activity
IDA
PMID:7954834
Alpha 9: an acetylcholine receptor with novel pharmacologica...
ACCEPT
Summary: ACh evokes cation currents through the receptor assembled from these subunits.
Reason: Rat recombinant/native comparisons are used at their stated species and assay scope. The original IDA assertion (PMID:7954834) is retained in the payload; this assessment uses independent receptor measurements rather than a GO annotation as evidence.
GO:0022848 acetylcholine-gated monoatomic cation-selective channel activity
IEA
GO_REF:0000120
ACCEPT
Summary: ACh evokes cation currents through the receptor assembled from these subunits.
Reason: Rat recombinant/native comparisons are used at their stated species and assay scope. The original IEA assertion (GO_REF:0000120) is retained in the payload; this assessment uses independent receptor measurements rather than a GO annotation as evidence.
GO:0022848 acetylcholine-gated monoatomic cation-selective channel activity
ISO
GO_REF:0000121
ACCEPT
Summary: ACh evokes cation currents through the receptor assembled from these subunits.
Reason: Rat recombinant/native comparisons are used at their stated species and assay scope. The original ISO assertion (GO_REF:0000121) is retained in the payload; this assessment uses independent receptor measurements rather than a GO annotation as evidence.
GO:0022848 acetylcholine-gated monoatomic cation-selective channel activity
ISO
GO_REF:0000121
ACCEPT
Summary: ACh evokes cation currents through the receptor assembled from these subunits.
Reason: Rat recombinant/native comparisons are used at their stated species and assay scope. The original ISO assertion (GO_REF:0000121) is retained in the payload; this assessment uses independent receptor measurements rather than a GO annotation as evidence.
GO:0022848 acetylcholine-gated monoatomic cation-selective channel activity
ISO
GO_REF:0000121
ACCEPT
Summary: ACh evokes cation currents through the receptor assembled from these subunits.
Reason: Rat recombinant/native comparisons are used at their stated species and assay scope. The original ISO assertion (GO_REF:0000121) is retained in the payload; this assessment uses independent receptor measurements rather than a GO annotation as evidence.
GO:0034220 monoatomic ion transmembrane transport
IBA
GO_REF:0000033
MODIFY
Summary: The measured receptor conducts cations across the membrane, including calcium.
Reason: Refine the broad transport term to cation transmembrane transport, preserving monovalent and divalent flux rather than narrowing the entire current to calcium. The original IBA assertion (GO_REF:0000033) is retained in the payload; this assessment uses independent receptor measurements rather than a GO annotation as evidence.
Propagation Review
Root cause: NO FAILURE CORE
Sources checked:
PANTHER:PTN000434994 SUPPORTS TRANSFER
The inherited broad claim is retained as biologically sound; independent target receptor evidence supports the stated refinement. The historical IBD placement was not re-inferred.
Supporting Evidence:
GO:0034220 monoatomic ion transmembrane transport
IEA
GO_REF:0000002
MODIFY
Summary: The measured receptor conducts cations across the membrane, including calcium.
Reason: Refine the broad transport term to cation transmembrane transport, preserving monovalent and divalent flux rather than narrowing the entire current to calcium. The original IEA assertion (GO_REF:0000002) is retained in the payload; this assessment uses independent receptor measurements rather than a GO annotation as evidence.
Supporting Evidence:
GO:0042472 inner ear morphogenesis
ISO
GO_REF:0000121
KEEP AS NON CORE
Summary: The mouse alpha9 knockout source PMID:10402196 establishes abnormal maturation of cochlear efferent synaptic connections.
Reason: Retain this as an inferred, anatomically restricted contribution to inner-ear organization in rat, not a claim that alpha9 constructs the whole membranous labyrinth. The receptor-mediated activity is the plausible developmental contribution; direct rat morphogenetic experiments were not established here.
Supporting Evidence:
GO:0045211 postsynaptic membrane
IEA
GO_REF:0000002
ACCEPT
Summary: Native auditory receptors occupy the hair-cell postsynaptic membrane facing efferent cholinergic terminals.
Reason: Rat recombinant/native comparisons are used at their stated species and assay scope. The original IEA assertion (GO_REF:0000002) is retained in the payload; this assessment uses independent receptor measurements rather than a GO annotation as evidence.
GO:0050910 detection of mechanical stimulus involved in sensory perception of sound
ISO
GO_REF:0000121
MARK AS OVER ANNOTATED
Summary: The live GO definition specifies receipt of sound vibration and conversion into a molecular signal.
Reason: Alpha9/alpha10 instead receives efferent acetylcholine and modulates the sensory cell through ion-channel signaling. Native comparison and mouse knockout experiments support efferent control and synaptic integrity, not assignment of this receptor as the mechanical stimulus detector. This is a role-scope correction, not a claim of absent auditory function or an invented loss in the PAINT lineage.
Propagation Review
Root cause: TERM SCOPING PROBLEM
Sources checked:
MGI:MGI:1202403 UNRESOLVED
The live GO definition specifies receipt of sound vibration and conversion into a molecular signal. Alpha9/alpha10 instead receives efferent acetylcholine and modulates the sensory cell through ion-channel signaling. Native comparison and mouse knockout experiments support efferent control and synaptic integrity, not assignment of this receptor as the mechanical stimulus detector. This is a role-scope correction, not a claim of absent auditory function or an invented loss in the PAINT lineage.
GO:0051899 membrane depolarization
IBA
GO_REF:0000033
ACCEPT
Summary: The receptor itself produces an inward, depolarizing cation current under the tested ionic conditions.
Reason: In native hair cells this calcium entry recruits a separate potassium conductance that can dominate the net response and hyperpolarize the cell. Retain the direct depolarizing component without equating it with net excitatory auditory transmission.
GO:0051899 membrane depolarization
IEA
GO_REF:0000107
ACCEPT
Summary: The receptor itself produces an inward, depolarizing cation current under the tested ionic conditions.
Reason: In native hair cells this calcium entry recruits a separate potassium conductance that can dominate the net response and hyperpolarize the cell. Retain the direct depolarizing component without equating it with net excitatory auditory transmission.
GO:0051899 membrane depolarization
ISO
GO_REF:0000121
ACCEPT
Summary: The receptor itself produces an inward, depolarizing cation current under the tested ionic conditions.
Reason: In native hair cells this calcium entry recruits a separate potassium conductance that can dominate the net response and hyperpolarize the cell. Retain the direct depolarizing component without equating it with net excitatory auditory transmission.
GO:0051899 membrane depolarization
ISO
GO_REF:0000121
ACCEPT
Summary: The receptor itself produces an inward, depolarizing cation current under the tested ionic conditions.
Reason: In native hair cells this calcium entry recruits a separate potassium conductance that can dominate the net response and hyperpolarize the cell. Retain the direct depolarizing component without equating it with net excitatory auditory transmission.
GO:0060078 regulation of postsynaptic membrane potential
IEA
GO_REF:0000120
ACCEPT
Summary: Cation entry and downstream potassium-channel coupling regulate the hair-cell postsynaptic potential; the net sign can be inhibitory.
Reason: Rat recombinant/native comparisons are used at their stated species and assay scope. The original IEA assertion (GO_REF:0000120) is retained in the payload; this assessment uses independent receptor measurements rather than a GO annotation as evidence.
GO:0060079 excitatory postsynaptic potential
IEA
GO_REF:0000108
MARK AS OVER ANNOTATED
Summary: The logical inference from acetylcholine-gated cation-channel activity to an excitatory postsynaptic potential overstates the physiological sign.
Reason: Native alpha9-containing hair-cell receptors couple calcium entry to calcium-dependent potassium channels and inhibitory synaptic responses. Real inward cation current is retained separately; it does not by itself establish a net EPSP in the native sensory circuit.
Supporting Evidence:
PMID:10875922
neonatal inner hair cells are inhibited by cholinergic synaptic input before the onset of hearing.
GO:0070373 negative regulation of ERK1 and ERK2 cascade
IEA
GO_REF:0000117
KEEP AS NON CORE
Summary: Full PMID:20505147 tests rat RBL-2H3 mast/basophil cells: prolonged low-dose nicotine inhibits Fc-epsilon-RI-associated ERK signaling and cytokine/leukotriene production, with receptor-subunit knockdowns affecting the suppressive response.
Reason: Retain this context-specific signaling contribution. The proposed alpha7/alpha9/alpha10 hybrid is not a structurally established pentamer and the experiment does not establish nicotine agonism of the ordinary hair-cell alpha9alpha10 channel.
Supporting Evidence:
GO:0070373 negative regulation of ERK1 and ERK2 cascade
IMP
PMID:20505147
Nicotine inhibits Fc epsilon RI-induced cysteinyl leukotrien...
KEEP AS NON CORE
Summary: Full PMID:20505147 tests rat RBL-2H3 mast/basophil cells: prolonged low-dose nicotine inhibits Fc-epsilon-RI-associated ERK signaling and cytokine/leukotriene production, with receptor-subunit knockdowns affecting the suppressive response.
Reason: Retain this context-specific signaling contribution. The proposed alpha7/alpha9/alpha10 hybrid is not a structurally established pentamer and the experiment does not establish nicotine agonism of the ordinary hair-cell alpha9alpha10 channel.
Supporting Evidence:
GO:0080164 regulation of nitric oxide metabolic process
ISO
GO_REF:0000121
UNDECIDED
Summary: The transfer names human CHRNA9/Q9UGM1 (including a processed-chain identifier), but the current human review and inspected human channel/structural sources do not identify the nitric-oxide pathway experiment underlying this rat claim.
Reason: Neither calcium permeability nor expression establishes that specific metabolic regulation. The source mechanism remains unresolved; this is not evidence that nitric-oxide effects are impossible.
Propagation Review
Root cause: UNRESOLVED
Sources checked:
UniProtKB:Q9UGM1 UNRESOLVED
The transfer names human CHRNA9/Q9UGM1 (including a processed-chain identifier), but the current human review and inspected human channel/structural sources do not identify the nitric-oxide pathway experiment underlying this rat claim. Neither calcium permeability nor expression establishes that specific metabolic regulation. The source mechanism remains unresolved; this is not evidence that nitric-oxide effects are impossible.
UniProtKB:Q9UGM1-PRO_0000000371 UNRESOLVED
The transfer names human CHRNA9/Q9UGM1 (including a processed-chain identifier), but the current human review and inspected human channel/structural sources do not identify the nitric-oxide pathway experiment underlying this rat claim. Neither calcium permeability nor expression establishes that specific metabolic regulation. The source mechanism remains unresolved; this is not evidence that nitric-oxide effects are impossible.
Supporting Evidence:
GO:0095500 acetylcholine receptor signaling pathway
IEA
GO_REF:0000107
ACCEPT
Summary: ACh binding is coupled to channel gating and calcium-dependent downstream signaling.
Reason: Rat recombinant/native comparisons are used at their stated species and assay scope. The original IEA assertion (GO_REF:0000107) is retained in the payload; this assessment uses independent receptor measurements rather than a GO annotation as evidence.
GO:0095500 acetylcholine receptor signaling pathway
ISO
GO_REF:0000121
ACCEPT
Summary: ACh binding is coupled to channel gating and calcium-dependent downstream signaling.
Reason: Rat recombinant/native comparisons are used at their stated species and assay scope. The original ISO assertion (GO_REF:0000121) is retained in the payload; this assessment uses independent receptor measurements rather than a GO annotation as evidence.
GO:0097060 synaptic membrane
IEA
GO_REF:0000044
MODIFY
Summary: The relevant auditory receptor pool is on the postsynaptic hair-cell plasma membrane.
Reason: Refine this general membrane location to the already represented postsynaptic membrane; recombinant surface currents corroborate membrane insertion but are not native localization measurements. The original IEA assertion (GO_REF:0000044) is retained in the payload; this assessment uses independent receptor measurements rather than a GO annotation as evidence.
Proposed replacements: postsynaptic membrane
Supporting Evidence:
GO:0098981 cholinergic synapse
EXP
PMID:10875922
Cholinergic synaptic inhibition of inner hair cells in the n...
ACCEPT
Summary: Native hair-cell cholinergic synapses contain the alpha9/alpha10 receptor pair.
Reason: Rat recombinant/native comparisons are used at their stated species and assay scope. The original EXP assertion (PMID:10875922) is retained in the payload; this assessment uses independent receptor measurements rather than a GO annotation as evidence.
GO:0098981 cholinergic synapse
IDA
PMID:10875922
Cholinergic synaptic inhibition of inner hair cells in the n...
ACCEPT
Summary: Native hair-cell cholinergic synapses contain the alpha9/alpha10 receptor pair.
Reason: Rat recombinant/native comparisons are used at their stated species and assay scope. The original IDA assertion (PMID:10875922) is retained in the payload; this assessment uses independent receptor measurements rather than a GO annotation as evidence.
GO:0098981 cholinergic synapse
IDA
PMID:18420419
Muscle-like nicotinic receptor accessory molecules in sensor...
ACCEPT
Summary: Native hair-cell cholinergic synapses contain the alpha9/alpha10 receptor pair.
Reason: Rat recombinant/native comparisons are used at their stated species and assay scope. The original IDA assertion (PMID:18420419) is retained in the payload; this assessment uses independent receptor measurements rather than a GO annotation as evidence.
GO:0098981 cholinergic synapse
IEA
GO_REF:0000117
ACCEPT
Summary: Native hair-cell cholinergic synapses contain the alpha9/alpha10 receptor pair.
Reason: Rat recombinant/native comparisons are used at their stated species and assay scope. The original IEA assertion (GO_REF:0000117) is retained in the payload; this assessment uses independent receptor measurements rather than a GO annotation as evidence.
GO:0099565 chemical synaptic transmission, postsynaptic
IEA
GO_REF:0000108
ACCEPT
Summary: This receptor mediates postsynaptic reception of efferent transmitter; it is not the presynaptic ACh release machinery.
Reason: Rat recombinant/native comparisons are used at their stated species and assay scope. The original IEA assertion (GO_REF:0000108) is retained in the payload; this assessment uses independent receptor measurements rather than a GO annotation as evidence.
GO:0099634 postsynaptic specialization membrane
IDA
PMID:18420419
Muscle-like nicotinic receptor accessory molecules in sensor...
ACCEPT
Summary: The native receptor pool is in the specialized hair-cell postsynaptic membrane.
Reason: Rat recombinant/native comparisons are used at their stated species and assay scope. The original IDA assertion (PMID:18420419) is retained in the payload; this assessment uses independent receptor measurements rather than a GO annotation as evidence.
GO:1902495 transmembrane transporter complex
IBA
GO_REF:0000033
MODIFY
Summary: The complex is specifically an acetylcholine-gated receptor pentamer.
Reason: Refine the inherited general transmembrane-transporter-complex annotation to that identity; no exact native stoichiometry is deduced from a general family descriptor. The original IBA assertion (GO_REF:0000033) is retained in the payload; this assessment uses independent receptor measurements rather than a GO annotation as evidence.
Propagation Review
Root cause: NO FAILURE CORE
Sources checked:
PANTHER:PTN000434994 SUPPORTS TRANSFER
The inherited broad claim is retained as biologically sound; independent target receptor evidence supports the stated refinement. The historical IBD placement was not re-inferred.
Supporting Evidence:
GO:1904315 transmitter-gated monoatomic ion channel activity involved in regulation of postsynaptic membrane potential
EXP
PMID:10875922
Cholinergic synaptic inhibition of inner hair cells in the n...
MODIFY
Summary: Rat alpha9/alpha10 receptor assays resolve the channel to acetylcholine-gated cation transport.
Reason: The subunit supplies part of the pentameric pore and gating machinery; it is not being treated as a complete isolated channel. Refine to the existing specific MF. The original EXP assertion (PMID:10875922) is retained in the payload; this assessment uses independent receptor measurements rather than a GO annotation as evidence.
Supporting Evidence:
GO:1904315 transmitter-gated monoatomic ion channel activity involved in regulation of postsynaptic membrane potential
IDA
PMID:10875922
Cholinergic synaptic inhibition of inner hair cells in the n...
MODIFY
Summary: Rat alpha9/alpha10 receptor assays resolve the channel to acetylcholine-gated cation transport.
Reason: The subunit supplies part of the pentameric pore and gating machinery; it is not being treated as a complete isolated channel. Refine to the existing specific MF. The original IDA assertion (PMID:10875922) is retained in the payload; this assessment uses independent receptor measurements rather than a GO annotation as evidence.
Supporting Evidence:

Core Functions

Rat alpha9 contributes to the alpha9/alpha10 receptor pore and ACh-dependent gating. Native auditory inhibition results from coupling this cation current to a separate potassium conductance; the receptor is not itself a potassium channel or primary mechanical sound sensor. Rat alpha9 can form functional homomers in oocytes, but the native auditory receptor includes alpha10.

Supporting Evidence:

References

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Notes

(Chrna9-notes.md)

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