| Primary Identifier | MGI:1890500 | Organism | mouse, laboratory |
| Chromosome | 3 | NCBI Gene Number | 171166 |
| Mgi Type | protein coding gene |
| description | FUNCTION: Automated description from the Alliance of Genome Resources (Release 9.1.0) Enables monoatomic anion channel activity; potassium channel activity; and sodium channel activity. Acts upstream of or within inner ear auditory receptor cell differentiation and locomotory behavior. Located in cytoplasm and plasma membrane. Is expressed in intestine; sensory organ; and vibrissa. Orthologous to human MCOLN3 (mucolipin TRP cation channel 3). PHENOTYPE: Heterozygotes show normal/diluted/white hair patches, circling, hyperactivity, deafness, and reduced fertility. Homozygotes are white with small patches of color and show severe behavioral abnormalities, poor postnatal viability and are nearly infertile. [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
