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MT-ATP6

Gene

mitochondrially encoded ATP synthase membrane subunit 6

HGNCHGNC:7414EnsemblENSG00000198899NCBI Gene4508
Locus: gene with protein productLocation: mitochondria

Also known as

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

Also known asMTATP6 · RP · ATP6 · ATPase-6 · Su6m
View full nomenclature history (9)
Previous symbolsMTATP6, RP
Alias symbolsATP6, ATPase-6, Su6m
Previous namesATP synthase 6, mitochondrially encoded ATP synthase 6, spicular retinitis pigmentosa with dementia, seizures, ataxia, proximal muscle weakness and sensory deficit
Alias namesmitochondrially encoded ATP synthase membrane subunit a

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.

Optic Atrophy, Hereditary, Leber
MERRF Syndrome

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.

Mitochondrial complex V: ATP synthase subunitsMitochondrially encoded protein coding genes

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2021-05-26.
Open TargetsGene–disease associations from the Open Targets Platform.