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ATP5F1C

Gene

ATP synthase F1 subunit gamma

HGNCHGNC:833EnsemblENSG00000165629NCBI Gene509
Locus: gene with protein productLocation: 10p14

Also known as

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

Also known asATP5CL1 · ATP5C · ATP5C1
View full nomenclature history (4)
Previous symbolsATP5CL1, ATP5C, ATP5C1
Previous namesATP synthase, H+ transporting, mitochondrial F1 complex, gamma polypeptide 1

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.

late-onset Alzheimers disease
Glioblastoma
Adverse effect
Diabetes Mellitus, Type 2
Non-alcoholic Fatty Liver Disease
Neoplasms
Placental abruption

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 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.