ATP6V0E1

Gene

ATPase H+ transporting V0 subunit e1

HGNCHGNC:863 EnsemblENSG00000113732 NCBI Gene8992

Locus: gene with protein productLocation: 5q35.1

Also known as

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

Also known asATP6H · ATP6V0E · M9.2

View full nomenclature history (7)

Previous symbolsATP6H, ATP6V0E

Alias symbolsM9.2

Previous namesATPase, H+ transporting, lysosomal (vacuolar proton pump) 9kD, ATPase, H+ transporting, lysosomal 9kDa, V0 subunit e, ATPase, H+ transporting, lysosomal 9kDa, V0 subunit e1

Alias namesV-ATPase subunit e1

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.

Multiple Myeloma

Diabetes Mellitus

Colorectal Neoplasms

Paroxysmal tachycardia

Esophageal Squamous Cell Carcinoma

Neoplasms

Squamous Cell Carcinoma of Head and Neck

Alzheimer's Disease

Insulinoma

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 subunitsSmall nucleolar RNA protein coding host genes

Provenance

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

Open TargetsGene–disease associations from the Open Targets Platform.