| Primary Identifier | MGI:1916862 | Organism | mouse, laboratory |
| Chromosome | 15 | NCBI Gene Number | 69612 |
| Mgi Type | protein coding gene |
| description | FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.1.0) Predicted to act upstream of or within chromatin organization. Predicted to be located in several cellular components, including actin cytoskeleton; cytosol; and nucleoplasm. Predicted to be part of NSL complex. Is expressed in nervous system and retina nuclear layer. Orthologous to human KANSL2 (KAT8 regulatory NSL complex subunit 2). PHENOTYPE: Mice homozygous for a floxed allele deleted in the brain exhibit prenatal lethality, intraventricular hemorrhage, and enlarged lateral ventricles. [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
