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Protein Coding Gene : Slco1a5 solute carrier organic anion transporter family, member 1a5

Primary Identifier  MGI:1351865 Organism  mouse, laboratory
Chromosome  6 NCBI Gene Number  108096
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.0.0)

Predicted to enable bile acid transmembrane transporter activity; sodium-independent organic anion transmembrane transporter activity; and thyroid hormone transmembrane transporter activity. Predicted to be involved in bile acid and bile salt transport; intestinal absorption; and sodium-independent organic anion transport. Predicted to act upstream of or within lipid transport and monoatomic ion transport. Predicted to be located in basal plasma membrane and brush border membrane. Predicted to be active in basolateral plasma membrane. Is expressed in ear; nervous system; and thyroid gland. Orthologous to human SLCO1A2 (solute carrier organic anion transporter family member 1A2).
PHENOTYPE: Homozygous mutation of this gene results in decreased percentage of CD8 ells and increased percentage of B cells in the peripheral blood. [provided by MGI curators]
  • synonyms:
  • solute carrier organic anion transporter family, member 1a5,
  • Oatp3,
  • Slco1a5,
  • solute carrier family 21 (organic anion transporter), member 7,
  • Slc21a7

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Genome

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1 Involved In Mutations

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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

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Function

Mouse features --> Functions (GO terms)

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