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COQ8B

Gene

coenzyme Q8B

HGNCHGNC:19041EnsemblENSG00000123815NCBI Gene79934
Locus: gene with protein productLocation: 19q13.2

Also known as

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

Also known asADCK4 · FLJ12229 · COQ8
View full nomenclature history (4)
Previous symbolsADCK4
Alias symbolsFLJ12229, COQ8
Previous namesaarF domain containing kinase 4

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.

Nephrotic Syndrome
Retinitis Pigmentosa
Genetic Diseases, Inborn
Mitochondrial Diseases
Retinal Diseases
Pulmonary Disease, Chronic Obstructive
Inflammatory Bowel 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.

ADCK family

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2023-01-25.
Open TargetsGene–disease associations from the Open Targets Platform.