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DCUN1D3

defective in cullin neddylation 1 domain containing 3

HCNC Approved Symbol
DCUN1D3 (HGNC:28734)
Genomic Coordinates
16:20,854,925 - 20,900,358 (16p12.3)
Synonyms
MGC48972, FLJ41725, DKFZp686O0290, SCCRO3
Disease Associations
Currently, this gene is not associated with any human disease in OMIM.

Diagnosed Cases

There are no diagnosed cases at this time.
However, there are 3 patients* with variant(s) predicted to be damaging.*2 of the patients have been diagnosed with a variant in another gene.

DCUN1D3 - Gene browser | 3billion