| Primary Identifier | MGI:2138232 | Organism | mouse, laboratory |
| Chromosome | 1 | NCBI Gene Number | 269132 |
| Mgi Type | protein coding gene |
| description | FUNCTION: Automated description from the Alliance of Genome Resources (Release 8.0.0) Predicted to enable procollagen galactosyltransferase activity. Predicted to be located in endoplasmic reticulum lumen. Is expressed in axial skeleton; central nervous system; and retina. Orthologous to human COLGALT2 (collagen beta(1-O)galactosyltransferase 2). PHENOTYPE: Homozygous null mice exhibit more extensive hepatocellular injury following concanavalin A challenge, with increased levels of interleukins, increased CD25+CD69- subset and decreased CD25-CD69+ subset of CD4+ T cells, and increased CD4+ T cell apoptosis. [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
