| Primary Identifier | MGI:2152541 | Organism | mouse, laboratory |
| Chromosome | 17 | Mgi Type | heritable phenotypic marker |
| description | FUNCTION: Automated description from the Alliance of Genome Resources (Release 8.0.0) Used to study asphyxiating thoracic dystrophy. PHENOTYPE: Homozygotes for an ENU-induced mutation exhibit severe skeletal defects including shortened body axis, absence of proximal portions of the ribs causing reduction of chest cavity, abnormal vertebrae, cleft secondary palate, and perinatal lethality. [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
