| Primary Identifier | MGI:3646230 | Organism | mouse, laboratory |
| Chromosome | 5 | NCBI Gene Number | 624224 |
| Mgi Type | protein coding gene |
| description | FUNCTION: Automated description from the Alliance of Genome Resources (Release 9.1.0) Involved in auditory receptor cell stereocilium organization. Acts upstream of or within inner ear auditory receptor cell differentiation; sensory perception of sound; and stereocilium maintenance. Located in stereocilium bundle. Is expressed in cochlea; cochlear duct; eye; and inner ear. Human ortholog(s) of this gene implicated in autosomal recessive nonsyndromic deafness. Orthologous to human CLRN2 (clarin 2). PHENOTYPE: Mice homozygous for an ENU-induced allele exhibit nonsyndromic progressive hearing loss with a lack of fast-graded voltage responses. [provided by MGI curators] |
Features --> Cross References
Canonical gene --> CDSs in specific strains.
Canonical gene --> Exons in specific strains
Canonical gene --> Strain-specific IDs, biotypes, and locations
Canonical gene --> Transcripts in specific strains.
Features --> Overlapping features
