| Primary Identifier | MGI:88424 | Organism | mouse, laboratory |
| Chromosome | 2 | Mgi Type | heritable phenotypic marker |
| description | FUNCTION: Automated description from the Alliance of Genome Resources (Release 8.0.0) Used to study attention deficit hyperactivity disorder. PHENOTYPE: Homozygous animals die in utero. Heterozygous mutants exhibit abnormal posture, abnormal head movements, hyperactivity, microphthalmia, and abnormalities of the pigmented choroid. [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
