Solute carrier organic anion transporter family member 2A1

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

Solute carrier organic anion transporter family member 2A1, also known as the prostaglandin transporter (PGT), is a protein that in humans is encoded by the SLCO2A1 gene.[5]

PDBOrtholog search: PDBe RCSB
AliasesSLCO2A1, MATR1, OATP2A1, PGT, PHOAR2, SLC21A2, solute carrier organic anion transporter family member 2A1, PHOAD
Quick facts SLCO2A1, Available structures ...
SLCO2A1
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesSLCO2A1, MATR1, OATP2A1, PGT, PHOAR2, SLC21A2, solute carrier organic anion transporter family member 2A1, PHOAD
External IDsOMIM: 601460; MGI: 1346021; HomoloGene: 38077; GeneCards: SLCO2A1; OMA:SLCO2A1 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_005630

NM_033314

RefSeq (protein)

NP_005621

NP_201571

Location (UCSC)Chr 3: 133.93 – 134.05 MbChr 9: 102.87 – 102.97 Mb
PubMed search[3][4]
Wikidata
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This gene encodes a prostaglandin transporter that is a member of the 12-membrane-spanning organic anion-transporting polypeptide superfamily of transporters. The encoded protein may be involved in mediating the uptake and clearance of prostaglandins in numerous tissues.[5]

Clinical relevance

Mutations in this gene have been shown to cause primary hypertrophic osteoarthropathy,[6] specific form of chronic enteropathy.

References

Further reading

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