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ATP13A5

Gene

ATPase 13A5

HGNCHGNC:31789EnsemblENSG00000187527NCBI Gene344905
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 asFLJ16025
View full nomenclature history (2)
Alias symbolsFLJ16025
Previous namesATPase type 13A5

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.

Poisoning
Hodgkin's Disease
Ovarian neoplasm
Dermatitis, Phototoxic
Hypothyroidism

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 2023-07-17.
Open TargetsGene–disease associations from the Open Targets Platform.