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NDUFA13

Gene

NADH:ubiquinone oxidoreductase subunit A13

HGNCHGNC:17194EnsemblENSG00000186010NCBI Gene51079
Locus: gene with protein productLocation: 19p13.11

Also known as

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

Also known asCGI-39 · CDA016 · GRIM-19 · GRIM19 · B16.6
View full nomenclature history (7)
Alias symbolsCGI-39, CDA016, GRIM-19, GRIM19, B16.6
Previous namesNADH dehydrogenase (ubiquinone) 1 alpha subcomplex, 13
Alias namescomplex I B16.6 subunit

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.

Diabetes Mellitus, Type 2
Diabetes Mellitus
Polycystic Ovary Syndrome
Obesity 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.

NADH:ubiquinone oxidoreductase supernumerary 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.