Entity Details

Primary name SLCO2A1
Entity type gene
Source Source Link

Details

PrimaryID6578
RefseqGeneNG_031964
SymbolSLCO2A1
Namesolute carrier organic anion transporter family member 2A1
Chromosome3
Location3q22.1-q22.2
TaxID9606
Statuslive
SourceGenomegenomic
SourceOriginnatural
CreationDate1998-08-12
ModificationDate2021-06-11

Ontological Relatives

UniProt IDsSO2A1_HUMAN

GO terms

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GOName
GO:0005319 lipid transporter activity
GO:0005886 plasma membrane
GO:0005887 integral component of plasma membrane
GO:0006869 lipid transport
GO:0015132 prostaglandin transmembrane transporter activity
GO:0015347 sodium-independent organic anion transmembrane transporter activity
GO:0015732 prostaglandin transport
GO:0016020 membrane
GO:0043252 sodium-independent organic anion transport

Diseases

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Disease IDSourceNameDescription
614441 OMIMHypertrophic osteoarthropathy, primary, autosomal recessive, 2 (PHOAR2)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. The disease is caused by variants affecting the gene represented in this entry.

Interactions

1 interaction

InteractorPartnerSourcesPublicationsLink
SLCO2A1GRB2IntAct17474147 details