ABCG5

ATP-binding cassette, sub-family G (WHITE), member 5
Identifiers
SymbolsABCG5 ; STSL
External IDsOMIM: 605459 MGI: 1351659 HomoloGene: 31909 IUPHAR: 794 GeneCards: ABCG5 Gene
RNA expression pattern
More reference expression data
Orthologs
SpeciesHumanMouse
Entrez6424027409
EnsemblENSG00000138075ENSMUSG00000040505
UniProtQ9H222Q99PE8
RefSeq (mRNA)NM_022436NM_031884
RefSeq (protein)NP_071881NP_114090
Location (UCSC)Chr 2:
44.04 – 44.07 Mb
Chr 17:
84.66 – 84.68 Mb
PubMed search

ATP-binding cassette sub-family G member 5 is a protein that in humans is encoded by the ABCG5 gene.[1][2][3]

Function

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.[3]

Interactive pathway map

Click on genes, proteins and metabolites below to link to respective articles. [§ 1]

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|{{{bSize}}}px|alt=Statin Pathway edit|]]

Statin Pathway edit

  1. The interactive pathway map can be edited at WikiPathways: "Statin_Pathway_WP430".

See also

References

  1. Berge KE, Tian H, Graf GA, Yu L, Grishin NV, Schultz J et al. (Dec 2000). "Accumulation of dietary cholesterol in sitosterolemia caused by mutations in adjacent ABC transporters". Science 290 (5497): 1771–5. doi:10.1126/science.290.5497.1771. PMID 11099417.
  2. Lu K, Lee MH, Hazard S, Brooks-Wilson A, Hidaka H, Kojima H et al. (Aug 2001). "Two genes that map to the STSL locus cause sitosterolemia: genomic structure and spectrum of mutations involving sterolin-1 and sterolin-2, encoded by ABCG5 and ABCG8, respectively". American Journal of Human Genetics 69 (2): 278–90. doi:10.1086/321294. PMC 1201544. PMID 11452359.
  3. 3.0 3.1 "Entrez Gene: ABCG5 ATP-binding cassette, sub-family G (WHITE), member 5 (sterolin 1)".

Further reading

External links

This article incorporates text from the United States National Library of Medicine, which is in the public domain.