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DCUN1D2

Gene

defective in cullin neddylation 1 domain containing 2

HGNCHGNC:20328EnsemblENSG00000150401NCBI Gene55208
Locus: gene with protein productLocation: 13q34

Also known as

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

Also known asC13orf17 · FLJ10704 · FLJ20092
View full nomenclature history (5)
Previous symbolsC13orf17
Alias symbolsFLJ10704, FLJ20092
Previous nameschromosome 13 open reading frame 17, DCN1, defective in cullin neddylation 1, domain containing 2 (S. cerevisiae)

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
Dementia
Ovarian carcinoma
Ovarian Neoplasms
Takotsubo Cardiomyopathy
Neoplasms

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.

Provenance

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