ATP13A3

Gene

ATPase 13A3

HGNCHGNC:24113 EnsemblENSG00000133657 NCBI Gene79572

Locus: gene with protein productLocation: 3q29

Also known as

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

Also known asAFURS1

View full nomenclature history (4)

Alias symbolsAFURS1

Previous namesATPase type 13A3

Alias namesATPase family homolog up regulated in senescence cells, Polyamine-transporting ATPase 13A3

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.

Pulmonary arterial hypertension

Aortic Valve Stenosis

Alcohol drinking

Stroke

Aortic valve calcification

Neuroblastoma

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 orphan transporters

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2024-09-16.

Open TargetsGene–disease associations from the Open Targets Platform.