| Primary Identifier | MGI:2679272 | Organism | mouse, laboratory |
| Chromosome | 11 | NCBI Gene Number | 268515 |
| Mgi Type | protein coding gene |
| description | FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.1.0) Predicted to enable chromatin binding activity. Acts upstream of or within chromatin organization; locomotory behavior; and neuron differentiation. Is expressed in central nervous system and retina. Orthologous to human BAHCC1 (BAH domain and coiled-coil containing 1). PHENOTYPE: Homozygous mutation of this gene results in perinatal lethality for the majority of mutants. Those that survive exhibit hind leg motor dysfunction. [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
