| Primary Identifier | MGI:1916449 | Organism | mouse, laboratory |
| Chromosome | 10 | NCBI Gene Number | 213402 |
| Mgi Type | protein coding gene |
| description | FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.0.0) Involved in sperm axoneme assembly. Is expressed in brain; reproductive system; respiratory system; spinal cord; and thyroid gland. Used to study male infertility. Human ortholog(s) of this gene implicated in spermatogenic failure 38. Orthologous to human ARMC2 (armadillo repeat containing 2). PHENOTYPE: Mice homozygous for a knock-out allele exhibit male infertility, oligozoospermia, immotile sperm, and teratozoospermia associated with severe sperm flagellum malformations. [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
