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COX18

Gene

cytochrome c oxidase assembly factor COX18

HGNCHGNC:26801EnsemblENSG00000163626NCBI Gene285521
Locus: gene with protein productLocation: 4q13.3

Also known as

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

Also known asFLJ38991 · OXA1L2
View full nomenclature history (5)
Alias symbolsFLJ38991, OXA1L2
Previous namesCOX18 cytochrome c oxidase assembly homolog (S. cerevisiae), cytochrome c oxidase assembly homolog 18 (yeast), COX18, cytochrome c oxidase assembly factor

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.

Neurodegenerative Diseases
Charcot-Marie-Tooth Disease
Mitochondrial Diseases
Sialadenitis
Prostate carcinoma
Empyema, Pleural

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 factors

Provenance

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