ATP6V1D

Gene

ATPase H+ transporting V1 subunit D

HGNCHGNC:13527 EnsemblENSG00000100554 NCBI Gene51382

Locus: gene with protein productLocation: 14q23.3

Also known as

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

Also known asATP6M · VATD · VMA8

View full nomenclature history (6)

Previous symbolsATP6M

Alias symbolsVATD, VMA8

Previous namesATPase, H+ transporting, lysosomal (vacuolar proton pump), ATPase, H+ transporting, lysosomal 34kDa, V1 subunit D

Alias namesV-ATPase subunit D

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.

Alzheimer's Disease

Autosomal dominant macrothrombocytopenia

Rare hemorrhagic disorder due to a constitutional platelet anomaly

Acquired polycythemia vera

Sinoatrial node dysfunction and deafness

Major depressive disorder

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.

V-type ATPase subunits

Provenance

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

Open TargetsGene–disease associations from the Open Targets Platform.