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SLCO2A1 - solute carrier organic anion transporter family member 2A1
- Synonym(s) : OATP2A1, PGT
- Previous symbols and names : MATR1, Matrin F/G 1, SLC21A2, Solute carrier family 21 (prostaglandin transporter), member 2, solute carrier organic anion transporter family, member 2A1
- Type : gene with protein product
- Chromosomal location : 3q22.1-q22.2
- OMIM: 601460
- HGNC: 10955
- UniProtKB: Q92959
- Genatlas: SLCO2A1
- Ensembl: ENSG00000174640
- IUPHAR-DB: -
- Reactome: Q92959
- LOVD: SLCO2A1
Diseases list
- Disease-causing germline mutation(s) (loss of function) in Chronic enteropathy associated with SLCO2A1 gene
ORPHA:468641 
- Disease-causing germline mutation(s) (loss of function) in Pachydermoperiostosis
ORPHA:2796
: AssessedGene included in a panel of genes performed as part of a diagnostic test
Additional information
Patient-centred resources for this gene
Research activities on this gene
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