| Primary Identifier | MGI:1890220 | Organism | mouse, laboratory |
| Chromosome | 12 | NCBI Gene Number | 56696 |
| Mgi Type | protein coding gene |
| description | FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.1.0) Predicted to enable G protein-coupled receptor activity. Involved in negative regulation of G2/M transition of mitotic cell cycle. Acts upstream of or within G1/S transition of mitotic cell cycle. Predicted to be located in plasma membrane. Is expressed in cerebral cortex; long bone epiphyseal plate; and thymus primordium. Used to study autoimmune disease. Orthologous to human GPR132 (G protein-coupled receptor 132). PHENOTYPE: Mice homozygous for disruptions in this gene display a generally normal phenotype but eventually develop a "late onset lymphoproliferative autoimmune syndrome" [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
