| Primary Identifier | MGI:1201406 | Organism | mouse, laboratory |
| Chromosome | 8 | NCBI Gene Number | 20494 |
| Mgi Type | protein coding gene |
| description | FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.0.0) Predicted to enable bile acid:sodium symporter activity. Acts upstream of or within response to bacterium. Located in apical plasma membrane and microvillus. Is expressed in Peyer's patch; male reproductive gland or organ; metanephros; and small intestine. Human ortholog(s) of this gene implicated in intestinal disease. Orthologous to human SLC10A2 (solute carrier family 10 member 2). PHENOTYPE: Mice homozygous for disruptions in this gene are essentially indistinguishable from wild-type in terms of survival, gross appearance and behavior. However, they do have defects in lipid absorption from the intestine. [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
