SLCO1B3 solute carrier organic anion transporter family member 1B3 [ Homo sapiens (human) ]
Source: NCBI Gene (ID 28234)
Symbol: SLCO1B3
Full name: solute carrier organic anion transporter family member 1B3
Gene type: protein coding
RefSeq status: REVIEWED
Organism: Homo sapiens
Also known as: HBLRR; LST-2; LST-3TM13; LST3; OATP-8; OATP1B3; OATP8; SLC21A8
Summary: 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]
Expression: Restricted expression toward liver (RPKM 30.2)
Orthologs: mouse
Gene size: 106207bp
Exon count: 17