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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 7.1.0)

Predicted to enable bile acid:sodium symporter activity. Predicted to be involved in bile acid and bile salt transport. Predicted to act upstream of or within lipid transport and sodium ion transport. Located in membrane. Is expressed in 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:
  • Slc10a1,
  • Ntcp,
  • MGD-MRK-12936,
  • solute carrier family 10 (sodium/bile acid cotransporter family), member 1,
  • Na+/taurocholate cotransporting polypeptide,
  • sodium bile acid cotransporting polypeptide

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