| Primary Identifier | MGI:95786 | Organism | mouse, laboratory |
| Chromosome | UN | Mgi Type | heritable phenotypic marker |
| description | FUNCTION: Automated description from the Alliance of Genome Resources (Release 8.0.0) Used to study neurodegeneration with brain iron accumulation 2a. PHENOTYPE: Mice homozygous for a spontaneous mutation breed only rarely, display a dull hair coat and small body size, and progressively develop a hunched posture, shaky gait and hindlimb paralysis associated with generalized neuroaxonal dystrophy. [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
