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ATP6V0E2

Gene

ATPase H+ transporting V0 subunit e2

HGNCHGNC:21723EnsemblENSG00000171130NCBI Gene155066
Locus: gene with protein productLocation: 7q36.1

Also known as

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

Also known asC7orf32 · ATP6V0E2L
View full nomenclature history (6)
Previous symbolsC7orf32, ATP6V0E2L
Previous nameschromosome 7 open reading frame 32, ATPase, H+ transporting V0 subunit E isoform 2-like (rat), ATPase, H+ transporting V0 subunit e2
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.

Alzheimer's Disease
Heart Septal Defects, Ventricular
Leukoplakia, Oral
Meniere's Disease
Carcinoma, Renal Cell
Bacteremia
Psoriasis
Leukemia, Myeloid, Acute

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