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NDUFA9

Gene

NADH:ubiquinone oxidoreductase subunit A9

HGNCHGNC:7693EnsemblENSG00000139180NCBI Gene4704
Locus: gene with protein productLocation: 12p13.3

Also known as

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

Also known asNDUFS2L · SDR22E1 · CI-39k · COQ11
View full nomenclature history (8)
Previous symbolsNDUFS2L
Alias symbolsSDR22E1, CI-39k, COQ11
Previous namesNADH dehydrogenase (ubiquinone) 1 alpha subcomplex, 9 (39kD), NADH dehydrogenase (ubiquinone) 1 alpha subcomplex, 9, 39kDa
Alias namesshort chain dehydrogenase/reductase family 22E, member 1, complex I 39kDa 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.

Parkinson's Disease
Diabetes Mellitus
Neurodegenerative Diseases
Multiple Sclerosis
Alzheimer's Disease
Lysosomal Storage Diseases

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.

Short chain dehydrogenase/reductase superfamilyNADH:ubiquinone oxidoreductase supernumerary subunitsFlavoproteins

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2023-01-20.
Open TargetsGene–disease associations from the Open Targets Platform.