disease:Defects in OTOA are the cause of non-syndromic sensorineural deafness autosomal recessive type 22 (DFNB22) [MIM:607039]. DFNB22 is a form of 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.,function:May act as an adhesion molecule.,similarity:Belongs to the stereocilin family.,subcellular location:At the interface between the apical surface of the epithelia and the overlying acellular gel of the tectorial and otoconial membranes.,
Apical cell membrane ; Lipid-anchor, GPI-anchor ; Extracellular side . Secreted, extracellular space, extracellular matrix . At the interface between the apical surface of the epithelia and the overlying acellular gel of the tectorial and otoconial membranes. .
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