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ATP7B

Gene

ATPase copper transporting beta

HGNCHGNC:870EnsemblENSG00000123191NCBI Gene540
Locus: gene with protein productLocation: 13q14.3

Also known as

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

Also known asWND
View full nomenclature history (6)
Previous symbolsWND
Previous namesATPase, Cu++ transporting, beta polypeptide (Wilson disease), ATPase, Cu++ transporting, beta polypeptide
Alias namesWilson disease, copper pump 2, copper-transporting ATPase 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.

Hepatolenticular Degeneration
Genetic Diseases, Inborn
Genetic developmental and epileptic encephalopathy
Hearing loss, autosomal recessive

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.

ATPase copper transporting

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2024-09-13.
Open TargetsGene–disease associations from the Open Targets Platform.