Proteins/UNIPROT:P58418

CLRN1

ProteinUNIPROT:P58418

May have a role in the excitatory ribbon synapse junctions between hair cells and cochlear ganglion cells and presumably also in analogous synapses within the retina..

Function from UniProtKB (P58418), read 2026-09-23. CC BY 4.0.

Curated compounds routed: 0

What the reference databases state

GenCC submitters' classifications

4 rows

retinitis pigmentosa has a germline basis in CLRN1DiseaseGenCC HGNC:12605|MONDO:0019200Inferred only
retinitis pigmentosa 61 has a germline basis in CLRN1DiseaseGenCC HGNC:12605|MONDO:0013610Inferred only
Usher syndrome type 3 has a germline basis in CLRN1DiseaseGenCC HGNC:12605|MONDO:0016485Inferred only
Usher syndrome type 3A has a germline basis in CLRN1DiseaseGenCC HGNC:12605|MONDO:0010170Inferred only

Statements

4 statements

4 statements · 2 reference databases · Subject: CLRN1 · Sources: gene ontology, Hetionet

Order

CLRN1 covaries with HLA-DPA1ProteinHetionet hetionet:covaries:3113-7401Inferred only
CLRN1 covaries with OR13C4ProteinHetionet hetionet:covaries:138804-7401Inferred only
CLRN1 covaries with ZNF432ProteinHetionet hetionet:covaries:7401-9668Inferred only
CLRN1 regulates positive regulation of lamellipodium assemblyBiological processgene ontology P58418|GO:0010592Inferred only

Other names

3 names

Resolves to: CLRN1

Also called: Clarin-1USH3AUsher syndrome type-3 protein

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