| Primary Identifier | MGI:3577767 | Organism | mouse, laboratory |
| Chromosome | 5 | NCBI Gene Number | 433899 |
| Mgi Type | protein coding gene |
| description | FUNCTION: Automated description from the Alliance of Genome Resources (Release 8.0.0) Involved in inner ear receptor cell stereocilium organization; sensory perception of sound; and vestibular receptor cell development. Acts upstream of or within cochlea development and inner ear auditory receptor cell differentiation. Located in kinocilium and stereocilium. Is expressed in endolymphatic duct; inner ear vestibular component; and utricle. Human ortholog(s) of this gene implicated in autosomal recessive nonsyndromic deafness 25. Orthologous to human GRXCR1 (glutaredoxin and cysteine rich domain containing 1). PHENOTYPE: Homozygous mutations at this locus result in circling and head tossing behavior, and impaired hearing. [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
