| Primary Identifier | MGI:1915585 | Organism | mouse, laboratory |
| Chromosome | 11 | NCBI Gene Number | 55978 |
| Mgi Type | protein coding gene |
| description | FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.1.0) Enables opsin binding activity. Involved in regulation of organelle assembly; regulation of platelet-derived growth factor receptor-alpha signaling pathway; and spermatogenesis. Acts upstream of or within several processes, including morphogenesis of a polarized epithelium; plasma membrane bounded cell projection organization; and protein transport. Located in several cellular components, including ciliary base; microtubule cytoskeleton; and photoreceptor cell cilium. Part of intraciliary transport particle B. Is expressed in cranium. Orthologous to human IFT20 (intraflagellar transport 20). PHENOTYPE: Mice homozygous for a null mutation die before birth. Mice with conditional loss in renal collecting ducts lack primary cilia and develop renal cysts. [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
