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BCS1L

Gene

BCS1 ubiquinol-cytochrome c reductase complex chaperone

HGNCHGNC:1020EnsemblENSG00000074582NCBI Gene617
Locus: gene with protein productLocation: 2q35

Also known as

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

Also known asHs.6719 · BCS · h-BCS · BJS
View full nomenclature history (11)
Alias symbolsHs.6719, BCS, h-BCS, BJS
Previous namesBCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone, BCS1 (yeast homolog)-like, BCS1-like (yeast), BCS1-like (S. cerevisiae), BC1 (ubiquinol-cytochrome c reductase) synthesis-like
Alias namesGRACILE syndrome, Bjornstad syndrome

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

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.

AAA ATPasesMitochondrial respiratory chain complex assembly factors

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2025-06-27.
Open TargetsGene–disease associations from the Open Targets Platform.