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SLCO2A1

Gene

solute carrier organic anion transporter family member 2A1

HGNCHGNC:10955EnsemblENSG00000174640NCBI Gene6578
Locus: gene with protein productLocation: 3q22.1-q22.2

Also known as

Symbols and names change; identity (the HGNC ID) does not. Previous and alternative forms are kept distinct.

Also known asSLC21A2 · MATR1 · PGT · OATP2A1
View full nomenclature history (8)
Previous symbolsSLC21A2, MATR1
Alias symbolsPGT, OATP2A1
Previous namessolute carrier family 21 (prostaglandin transporter), member 2, matrin F/G 1, solute carrier organic anion transporter family, member 2A1
Alias namesprostaglandin transporter

Associated diseases

via associated_with

Diseases linked to this gene through the canonical GENE→DISEASE (associated_with) relation, drawn from Open Targets' top-ranked associations by overall score — not the full association set. Disease-level detail lives on each disease's own page.

Osteoarthropathy, Primary Hypertrophic
Hypertension, Pregnancy-Induced
Alzheimer's Disease
Male reproductive organ cancer
Poisoning
Parkinson's Disease
Neurodegenerative Diseases

Drawn from Open Targets’ top 10 associations by overall score for this gene — the subset resolved to a canonical disease. Lower-ranked associations, and diseases not yet canonicalised, are not shown.

Gene family

HGNC gene-group membership.

Solute carrier organic anion transporter family

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2023-01-20.
Open TargetsGene–disease associations from the Open Targets Platform.