| Primary Identifier | MGI:2180716 | Organism | mouse, laboratory |
| Chromosome | X | Mgi Type | heritable phenotypic marker |
| description | FUNCTION: Automated description from the Alliance of Genome Resources (Release 8.0.0) Used to study X-linked dominant hypophosphatemic rickets. PHENOTYPE: Hemizygous males for an irradiation-induced X-linked deletion that disrupts both Sms and Phex genes show the hypophosphatemic rickets (found also in mice with lone Phex mutations) but also exhibit reduced viability, circling behavior, markedly reduced spermine content, and sterility. [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
