Homo sapiens Protein: SLCO1B1 | |||||||||||||||
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Summary | |||||||||||||||
InnateDB Protein | IDBP-22551.5 | ||||||||||||||
Last Modified | 2014-10-13 [Report errors or provide feedback] | ||||||||||||||
Gene Symbol | SLCO1B1 | ||||||||||||||
Protein Name | solute carrier organic anion transporter family, member 1B1 | ||||||||||||||
Synonyms | HBLRR; LST-1; LST1; OATP-C; OATP1B1; OATP2; OATPC; SLC21A6; | ||||||||||||||
Species | Homo sapiens | ||||||||||||||
Ensembl Protein | ENSP00000256958 | ||||||||||||||
InnateDB Gene | IDBG-22549 (SLCO1B1) | ||||||||||||||
Protein Structure | |||||||||||||||
UniProt Annotation | |||||||||||||||
Function | Mediates the Na(+)-independent uptake of organic anions such as pravastatin, taurocholate, methotrexate, dehydroepiandrosterone sulfate, 17-beta-glucuronosyl estradiol, estrone sulfate, prostaglandin E2, thromboxane B2, leukotriene C3, leukotriene E4, thyroxine and triiodothyronine. Involved in the clearance of bile acids and organic anions from the liver. {ECO:0000269PubMed:10358072, ECO:0000269PubMed:10601278, ECO:0000269PubMed:12196548, ECO:0000269PubMed:22232210}. | ||||||||||||||
Subcellular Localization | Basolateral cell membrane {ECO:0000269PubMed:12196548}; Multi-pass membrane protein {ECO:0000269PubMed:12196548}. Note=Detected in basolateral membranes of hepatocytes. | ||||||||||||||
Disease Associations | Hyperbilirubinemia, Rotor type (HBLRR) [MIM:237450]: An autosomal recessive form of primary conjugated hyperbilirubinemia. Affected individuals develop mild jaundice not associated with hemolysis shortly after birth or in childhood. They have delayed plasma clearance of the unconjugated anionic dye bromsulphthalein and prominent urinary excretion of coproporphyrin I. Hepatic pigmentation is normal. {ECO:0000269PubMed:22232210}. Note=The disease is caused by mutations affecting the gene represented in this entry. | ||||||||||||||
Tissue Specificity | Highly expressed in liver, at the basolateral membranes of centrilobular hepatocytes. Not detected in heart, brain, placenta, lung, skeletal muscle, kidney, pancreas, spleen, thymus, prostate, testis, ovary, small intestine, colon and leukocyte. {ECO:0000269PubMed:10358072, ECO:0000269PubMed:10601278, ECO:0000269PubMed:22232210}. | ||||||||||||||
Comments | |||||||||||||||
Interactions | |||||||||||||||
Number of Interactions |
This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
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Gene Ontology | |||||||||||||||
Molecular Function |
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Biological Process |
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Cellular Component |
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Protein Structure and Domains | |||||||||||||||
PDB ID | |||||||||||||||
InterPro |
IPR002350
Kazal domain IPR004156 Organic anion transporter polypeptide OATP IPR011701 Major facilitator superfamily IPR016196 Major facilitator superfamily domain, general substrate transporter IPR020846 Major facilitator superfamily domain |
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PFAM |
PF00050
PF07648 PF03137 PF07690 |
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PRINTS | |||||||||||||||
PIRSF | |||||||||||||||
SMART |
SM00280
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TIGRFAMs | |||||||||||||||
Post-translational Modifications | |||||||||||||||
Modification | |||||||||||||||
Cross-References | |||||||||||||||
SwissProt | Q9Y6L6 | ||||||||||||||
PhosphoSite | PhosphoSite-Q9Y6L6 | ||||||||||||||
TrEMBL | K4P403 | ||||||||||||||
UniProt Splice Variant | |||||||||||||||
Entrez Gene | 10599 | ||||||||||||||
UniGene | Hs.449738 | ||||||||||||||
RefSeq | NP_006437 | ||||||||||||||
HUGO | HGNC:10959 | ||||||||||||||
OMIM | 604843 | ||||||||||||||
CCDS | CCDS8685 | ||||||||||||||
HPRD | 09214 | ||||||||||||||
IMGT | |||||||||||||||
EMBL | AB026257 AF060500 AF205071 AJ132573 AJ400749 AJ400750 AJ400751 AJ400752 AJ400753 AJ400754 AJ400755 AJ400756 AJ400757 AJ400758 AJ400759 AJ400760 AJ400761 AJ400762 AK312970 AY945934 BC114376 CH471094 JX547014 | ||||||||||||||
GenPept | AAD38323 AAF20212 AAI14377 AAX20114 AFV58025 BAA78639 BAG35809 CAB62577 CAB97007 EAW96420 EAW96421 | ||||||||||||||