Back to discover

DCUN1D3

Gene

defective in cullin neddylation 1 domain containing 3

HGNCHGNC:28734EnsemblENSG00000188215NCBI Gene123879
Locus: gene with protein productLocation: 16p12.3

Also known as

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

Also known asMGC48972 · FLJ41725 · DKFZp686O0290 · SCCRO3
View full nomenclature history (5)
Alias symbolsMGC48972, FLJ41725, DKFZp686O0290, SCCRO3
Previous namesDCN1, defective in cullin neddylation 1, domain containing 3 (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.

PPARG-related familial partial lipodystrophy

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.