| Primary Identifier | MGI:2685402 | Organism | mouse, laboratory |
| Chromosome | 1 | NCBI Gene Number | 227357 |
| Mgi Type | protein coding gene |
| description | FUNCTION: Automated description from the Alliance of Genome Resources (Release 8.0.0) Enables actin filament binding activity. Involved in sensory perception of sound. Is active in stereocilium tip. Is expressed in metanephros; saccule; submandibular gland; and testis. Orthologous to human ESPNL (espin like). PHENOTYPE: Mice homozygous for a null allele exhibit high-frequency hearing loss and abnormal outer hair cell stereociliary bundle morphology, with the shortest row of stereocilia largely missing from the basal region, but no overt vestibular phenotype. [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
