Entity Details

Primary name OTOA
Entity type gene
Source Source Link

Details

PrimaryID146183
RefseqGeneNG_012973
SymbolOTOA
Nameotoancorin
Chromosome16
Location16p12.2
TaxID9606
Statuslive
SourceGenomegenomic
SourceOriginnatural
CreationDate2002-01-21
ModificationDate2021-06-11

Ontological Relatives

UniProt IDsOTOAN_HUMAN

GO terms

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GOName
GO:0005576 extracellular region
GO:0005886 plasma membrane
GO:0007160 cell-matrix adhesion
GO:0007605 sensory perception of sound
GO:0009986 cell surface
GO:0016324 apical plasma membrane
GO:0031225 anchored component of membrane

Diseases

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Disease IDSourceNameDescription
607039 OMIMDeafness, autosomal recessive, 22 (DFNB22)A form of non-syndromic sensorineural hearing loss. Sensorineural deafness results from damage to the neural receptors of the inner ear, the nerve pathways to the brain, or the area of the brain that receives sound information. The disease is caused by variants affecting the gene represented in this entry.

Interactions

5 interactions

InteractorPartnerSourcesPublicationsLink
OTOAAURKBBioGRID31586073 details
OTOAKIF14BioGRID31586073 details
OTOAKIF20ABioGRID31586073 details
OTOAKIF23BioGRID31586073 details
OTOAPRC1BioGRID31586073 details