| Primary Identifier | MGI:109188 | Organism | mouse, laboratory |
| Chromosome | 15 | NCBI Gene Number | 16564 |
| Mgi Type | protein coding gene |
| description | FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.1.0) Predicted to enable several functions, including ATP hydrolysis activity; ankyrin repeat binding activity; and microtubule binding activity. Predicted to be involved in microtubule-based movement. Predicted to be located in cytosol. Predicted to be part of kinesin complex. Predicted to be active in microtubule. Is expressed in several structures, including alimentary system; central nervous system; eye; immune system; and peripheral nervous system. Used to study congenital fibrosis of the extraocular muscles. Human ortholog(s) of this gene implicated in congenital fibrosis of the extraocular muscles 1. Orthologous to human KIF21A (kinesin family member 21A). PHENOTYPE: Nullizygous mice die neonatally with no apparent oculomotor nerve pathology. Mice harboring a humanized amino acid substitution show uni- or bilateral ptosis, globe retraction, reduced numbers of oculomotor nerve and abducens motor neurons, and altered extraocular muscle morphology and innervation. [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
