Entity Details

Primary name OTOAN_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionQ7RTW8
EntryNameOTOAN_HUMAN
FullNameOtoancorin
TaxID9606
Evidenceevidence at protein level
Length1153
SequenceStatuscomplete
DateCreated2004-12-07
DateModified2021-06-02

Ontological Relatives

GenesOTOA

GO terms

Show/Hide Table
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

Subcellular Location

Show/Hide Table
Subcellular Location
Apical cell membrane
Secreted

Domains

Show/Hide Table
DomainNameCategoryType
IPR026663 OtoancorinFamilyFamily
IPR026664 Stereocilin-relatedFamilyFamily

Diseases

Show/Hide Table
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

0 interactions

InteractorPartnerSourcesPublicationsLink