SLC31A2

Gene

solute carrier family 31 member 2

HGNCHGNC:11017 EnsemblENSG00000136867 NCBI Gene1318

Locus: gene with protein productLocation: 9q32

Also known as

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

Also known asCOPT2 · hCTR2 · CTR2

View full nomenclature history (5)

Previous symbolsCOPT2

Alias symbolshCTR2, CTR2

Previous namessolute carrier family 31 (copper transporter), member 2

Alias namescopper transporter 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.

Ovarian carcinoma

Hepatolenticular Degeneration

Adenocarcinoma of Lung

Hypertension

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 family 31

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2023-01-20.

Open TargetsGene–disease associations from the Open Targets Platform.