| Primary Identifier | MGI:1932139 | Organism | mouse, laboratory |
| Chromosome | 19 | NCBI Gene Number | 76055 |
| Mgi Type | protein coding gene |
| description | FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.0.0) Predicted to enable beta-N-acetylglucosaminidase activity; histone acetyltransferase activity; and identical protein binding activity. Predicted to be involved in several processes, including positive regulation of mitochondrial depolarization; positive regulation of transport; and regulation of protein metabolic process. Predicted to be located in cytosol. Is expressed in brain; liver; and retina nuclear layer. Orthologous to human OGA (O-GlcNAcase). PHENOTYPE: Mice homozygous for a gene-trapped allele exhibit perinatal lethality associated with a developmental delay and respiratory failure. Mouse embryonic fibroblasts exhibit proliferative and mitotic defects, frequent cytokinesis failure, and loss of genomic stability. [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
