ABCG5 ATP binding cassette subfamily G member 5 [ Homo sapiens (human) ]
Source: NCBI Gene (ID 64240)
Source: NCBI Gene (ID 64240)
Symbol: ABCG5
Full name: ATP binding cassette subfamily G member 5
Gene type: protein coding
RefSeq status: REVIEWED
Organism: Homo sapiens
Also known as: STSL; STSL2
Summary: The protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intra-cellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This protein is a member of the White subfamily. The protein encoded by this gene functions as a half-transporter to limit intestinal absorption and promote biliary excretion of sterols. It is expressed in a tissue-specific manner in the liver, colon, and intestine. This gene is tandemly arrayed on chromosome 2, in a head-to-head orientation with family member ABCG8. Mutations in this gene may contribute to sterol accumulation and atheroschlerosis, and have been observed in patients with sitosterolemia. [provided by RefSeq, Jul 2008]
Expression: Biased expression in duodenum (RPKM 25.9), small intestine (RPKM 24.3) and 1 other tissue
Orthologs: mouse
Gene size: 33021bp
Exon count: 16