COPS8

Gene

COP9 signalosome subunit 8

HGNCHGNC:24335 EnsemblENSG00000198612 NCBI Gene10920

Locus: gene with protein productLocation: 2q37.3

Also known as

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

Also known asCOP9 · CSN8 · MGC1297 · SGN8

View full nomenclature history (5)

Alias symbolsCOP9, CSN8, MGC1297, SGN8

Previous namesCOP9 constitutive photomorphogenic homolog subunit 8 (Arabidopsis)

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

Diabetes, Gestational

Anemia

Respiratory Tract 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.

COP9 signalosome

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2023-01-20.

Open TargetsGene–disease associations from the Open Targets Platform.