| Entrez gene ID | | 261738 |
| Official gene symbol | | Clrn1 |
| Full name | | clarin 1 |
| Aliases | | Ush3,Ush3a |
| Gene summary | | gene associated with Usher syndrome type III is an autosomal recessive disorder characterized by progressive sensorineural hearing loss, vestibular dysfunction, and retinitis pigmentosa [RGD] |
| Location | | Chromosome: 2 Locus: 2q31 |
| Gene position | | 148193632 - 148243574 Map Viewer |
| Gene orientation | | minus |
| Gene size | | 49943 bp |
| Gene sequence |
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