Homo sapiens Protein: SLCO2A1 | |||||||||||
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Summary | |||||||||||
InnateDB Protein | IDBP-57430.6 | ||||||||||
Last Modified | 2014-10-13 [Report errors or provide feedback] | ||||||||||
Gene Symbol | SLCO2A1 | ||||||||||
Protein Name | solute carrier organic anion transporter family, member 2A1 | ||||||||||
Synonyms | MATR1; OATP2A1; PGT; PHOAR2; SLC21A2; | ||||||||||
Species | Homo sapiens | ||||||||||
Ensembl Protein | ENSP00000311291 | ||||||||||
InnateDB Gene | IDBG-57428 (SLCO2A1) | ||||||||||
Protein Structure |
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UniProt Annotation | |||||||||||
Function | May mediate the release of newly synthesized prostaglandins from cells, the transepithelial transport of prostaglandins, and the clearance of prostaglandins from the circulation. Transports PGD2, as well as PGE1, PGE2 and PGF2A. | ||||||||||
Subcellular Localization | Cell membrane; Multi-pass membrane protein. | ||||||||||
Disease Associations | Hypertrophic osteoarthropathy, primary, autosomal recessive, 2 (PHOAR2) [MIM:614441]: A disease characterized by digital clubbing, periostosis, acroosteolysis, painful joint enlargement, and variable features of pachydermia that include thickened facial skin and a thickened scalp. Other developmental anomalies include delayed closure of the cranial sutures and congenital heart disease. {ECO:0000269PubMed:22197487, ECO:0000269PubMed:22331663, ECO:0000269PubMed:22553128, ECO:0000269PubMed:22696055}. Note=The disease is caused by mutations affecting the gene represented in this entry. | ||||||||||
Tissue Specificity | Ubiquitous. Significant expression observed in ling, kidney, spleen, and heart. {ECO:0000269PubMed:22331663}. | ||||||||||
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 | Q92959 | ||||||||||
PhosphoSite | PhosphoSite- | ||||||||||
TrEMBL | Q4LEJ9 | ||||||||||
UniProt Splice Variant | |||||||||||
Entrez Gene | 6578 | ||||||||||
UniGene | Hs.706549 | ||||||||||
RefSeq | NP_005621 | ||||||||||
HUGO | HGNC:10955 | ||||||||||
OMIM | 601460 | ||||||||||
CCDS | CCDS3084 | ||||||||||
HPRD | 03269 | ||||||||||
IMGT | |||||||||||
EMBL | AB201109 AB201110 AF056719 AF056720 AF056721 AF056722 AF056723 AF056724 AF056725 AF056726 AF056727 AF056728 AF056729 AF056730 AF056731 AF056732 BC041140 BC051347 CH471052 U70867 | ||||||||||
GenPept | AAC09469 AAC62004 AAH41140 AAH51347 BAE03223 BAE03224 EAW79156 | ||||||||||