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SCO2

Gene

synthesis of cytochrome C oxidase 2

HGNCHGNC:10604EnsemblENSG00000284194NCBI Gene9997
Locus: gene with protein productLocation: 22q13.33

Also known as

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

Also known asMYP6 · SCO1L
View full nomenclature history (7)
Previous symbolsMYP6
Alias symbolsSCO1L
Previous namesSCO (cytochrome oxidase deficient, yeast) homolog 2, SCO cytochrome oxidase deficient homolog 2 (yeast), myopia 6, SCO2, cytochrome c oxidase assembly protein, SCO cytochrome c oxidase assembly protein 2

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
Neurodegenerative Diseases
Genetic Diseases, Inborn

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.