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ABCC2

Gene

ATP binding cassette subfamily C member 2

HGNCHGNC:53EnsemblENSG00000023839NCBI Gene1244
Locus: gene with protein productLocation: 10q24.2

Also known as

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

Also known asCMOAT · DJS · MRP2 · cMRP
View full nomenclature history (6)
Previous symbolsCMOAT
Alias symbolsDJS, MRP2, cMRP
Previous namescanalicular multispecific organic anion transporter 1, ATP-binding cassette, sub-family C (CFTR/MRP), member 2

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.

Cholestasis
Genetic Diseases, Inborn
Hypothyroidism
Cataract
Progressive familial intrahepatic cholestasis

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.

ATP binding cassette subfamily C

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2024-09-16.
Open TargetsGene–disease associations from the Open Targets Platform.