| Entrez gene ID | | 25861 |
| Official gene symbol | | DFNB31 |
| Full name | | deafness, autosomal recessive 31 |
| Aliases | | ,CIP98,DKFZp434N014,KIAA1526,RP11-9M16.1,USH2D,WHRN,WI, |
| Gene summary | | This gene is thought to function in the organization and stabilization of sterocilia elongation and actin cystoskeletal assembly, based on studies of the related mouse gene. Mutations in this gene have been associated with autosomal recessive non-syndromic deafness and Usher Syndrome. Alternative splicing of this gene results in multiple transcript variants encoding different isoforms. |
| Location | | Chromosome: 9 Locus: 9q32-q34 |
| Gene position | | 117267736 - 117164360 Map Viewer |
| Gene orientation | | minus |
| Gene size | | 103377 bp |
| Gene sequence |
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| OMIM ID | | 607928 |
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