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Protein Coding Gene : Slc10a1 solute carrier family 10 (sodium/bile acid cotransporter family), member 1

Primary Identifier  MGI:97379 Organism  mouse, laboratory
Chromosome  12 NCBI Gene Number  20493
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 8.0.0)

Predicted to enable bile acid:sodium symporter activity. Predicted to be involved in bile acid and bile salt transport. Located in membrane. Is expressed in 1-cell stage embryo; 2-cell stage embryo; and liver. Orthologous to human SLC10A1 (solute carrier family 10 member 1).
PHENOTYPE: Mice homozygous for a knock-out allele show impaired hepatic uptake of conjugated bile acids (BAs) and Myrcludex B binding. A subset of adult homozygotes exhibit hypercholanemia, reduced body weight, increased serum alkaline phosphatase and bilirubin levels but no overt liver damage. [provided by MGI curators]
  • synonyms:
  • Na+/taurocholate cotransporting polypeptide,
  • MGD-MRK-12936,
  • Slc10a1,
  • solute carrier family 10 (sodium/bile acid cotransporter family), member 1,
  • sodium bile acid cotransporting polypeptide,
  • Ntcp

Features --> Cross References

Genome

Sequence Feature Displayer

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0 Canonical

0 CDSs

0 Exons

0 Genomic Clusters

1 Involved In Mutations

0 Strain

0 Transcripts

0 Transgenic Expressors

0 UTRs

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

Proteins

Gene --> Proteins

Function

Mouse features --> Functions (GO terms)

Homology

Genes --> Homologs

Interactions

5 Pathways

0 Targeted By

Gene --> Protein-Protein Interactions

Expression

Gene --> Expression annotations

Phenotype

Genes/Features --> Phenotypes (MP terms)

Disease

Mouse features --> Human diseases

Literature

Mouse features --> Publications

 

Other

0 Driver For