SLCO1B3 Chromosome 12

Solute carrier organic anion transporter family member 1B3
15 variants 15 Health Risk

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What This Gene Does
This gene encodes a liver-specific member of the organic anion transporter family. The encoded protein is a transmembrane receptor that mediates the sodium-independent uptake of endogenous and xenobiotic compounds and plays a critical role in bile acid and bilirubin transport. Mutations in this gene are a cause of Rotor type hyperbilirubinemia. Alternative splicing of this gene and the use of alternative promoters results in transcript variants encoding different isoforms that differ in their tissue specificity. [provided by RefSeq, Mar 2017]
Gene Info
Gene Group
Solute carrier organic anion transporter family
Locus Type
gene with protein product
Location
12p12.2
Ensembl
ENSG00000111700
Associated Conditions (2)
Rotor syndrome
SLCO1B3-related disorder
Key Variants
All Variants (15)
RSID Category Clinical Significance Conditions
RS12299012 Health Risk Conflicting classifications of pathogenicity Rotor syndrome, Rotor syndrome
RS142694767 Health Risk Conflicting classifications of pathogenicity Rotor syndrome, SLCO1B3-related disorder, Rotor syndrome
RS145036538 Health Risk Conflicting classifications of pathogenicity Rotor syndrome, Rotor syndrome
RS145334570 Health Risk Conflicting classifications of pathogenicity Rotor syndrome, Rotor syndrome
RS146623116 Health Risk Conflicting classifications of pathogenicity Rotor syndrome, SLCO1B3-related disorder, Rotor syndrome
RS180875376 Health Risk Conflicting classifications of pathogenicity Rotor syndrome, SLCO1B3-related disorder, Rotor syndrome
RS369736559 Health Risk Conflicting classifications of pathogenicity Rotor syndrome, Rotor syndrome
RS370334648 Health Risk Conflicting classifications of pathogenicity Rotor syndrome, SLCO1B3-related disorder, Rotor syndrome
RS4149143 Health Risk Conflicting classifications of pathogenicity Rotor syndrome, SLCO1B3-related disorder, Rotor syndrome
RS558592800 Health Risk Conflicting classifications of pathogenicity Rotor syndrome, SLCO1B3-related disorder, Rotor syndrome
RS777458586 Health Risk Conflicting classifications of pathogenicity Rotor syndrome, SLCO1B3-related disorder, Rotor syndrome
RS201833947 Health Risk Likely pathogenic Rotor syndrome, Rotor syndrome
RS140033394 Health Risk Pathogenic Rotor syndrome, SLCO1B3-related disorder, Rotor syndrome
RS373707046 Health Risk Pathogenic Rotor syndrome, SLCO1B3-related disorder, Rotor syndrome
RS78627909 Health Risk Pathogenic Rotor syndrome, SLCO1B3-related disorder, Rotor syndrome
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