Back to discover

NDUFAF5

Gene

NADH:ubiquinone oxidoreductase complex assembly factor 5

HGNCHGNC:15899EnsemblENSG00000101247NCBI Gene79133
Locus: gene with protein productLocation: 20p12.1

Also known as

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

Also known asC20orf7 · dJ842G6.1
View full nomenclature history (4)
Previous symbolsC20orf7
Alias symbolsdJ842G6.1
Previous nameschromosome 20 open reading frame 7, NADH dehydrogenase (ubiquinone) complex I, assembly factor 5

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.

Mitochondrial Diseases
Genetic Diseases, Inborn
Neurodegenerative Diseases
Benign prostatic hyperplasia

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 respiratory chain complex assembly factors7BS non-methyltransferases

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2023-03-15.
Open TargetsGene–disease associations from the Open Targets Platform.