| Primary Identifier | MGI:104728 | Organism | mouse, laboratory |
| Chromosome | 13 | NCBI Gene Number | 12328 |
| Mgi Type | protein coding gene |
| description | FUNCTION: Automated description from the Alliance of Genome Resources (Release 8.0.0) Predicted to enable cell adhesion molecule binding activity and ubiquitin protein ligase binding activity. Involved in B cell homeostasis. Acts upstream of or within epidermal growth factor receptor signaling pathway and receptor recycling. Predicted to be located in endoplasmic reticulum membrane. Predicted to be part of GET complex. Is expressed in central nervous system; dorsal root ganglion; and retina. Human ortholog(s) of this gene implicated in congenital disorder of glycosylation type II. Orthologous to human CAMLG (calcium modulating ligand). PHENOTYPE: Mice lacking both functional copies of this gene die during early gestation. [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
