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ERCC6

Gene

ERCC excision repair 6, chromatin remodeling factor

HGNCHGNC:3438EnsemblENSG00000225830NCBI Gene2074
Locus: gene with protein productLocation: 10q11.23

Also known as

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

Also known asCKN2 · CSB · RAD26 · ARMD5
View full nomenclature history (7)
Previous symbolsCKN2
Alias symbolsCSB, RAD26, ARMD5
Previous namesexcision repair cross-complementing rodent repair deficiency, complementation group 6, excision repair cross-complementation group 6
Alias namesCockayne syndrome B protein

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.

Cockayne Syndrome
Lung Neoplasms
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.

SNF2 related familyERCC excision repair associatedB-WICH chromatin-remodelling complex subunits

Provenance

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