| Primary Identifier | MGI:1929215 | Organism | mouse, laboratory |
| Chromosome | 13 | NCBI Gene Number | 218035 |
| Mgi Type | protein coding gene |
| description | FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.1.0) Enables microtubule binding activity. Predicted to be involved in several processes, including endosomal vesicle fusion; macroautophagy; and vacuolar transport. Predicted to act upstream of or within autophagy and protein transport. Located in early endosome; late endosome; and microtubule cytoskeleton. Is expressed in embryo; extraembryonic component; and primitive endoderm. Human ortholog(s) of this gene implicated in autosomal recessive spinocerebellar ataxia 29. Orthologous to human VPS41 (VPS41 subunit of HOPS complex). PHENOTYPE: Embryos homozygous for a knock-out allele die by E9 exhibiting morphological and functional alteration of late endocytic compartments, and abnormal triploblastic development. [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
