DCUN1D5 defective in cullin neddylation 1 domain containing 5 [ Homo sapiens (human) ]
Source: NCBI Gene (ID 84259)
Symbol: DCUN1D5
Full name: defective in cullin neddylation 1 domain containing 5
Gene type: protein coding
RefSeq status: VALIDATED
Organism: Homo sapiens
Also known as: DCNL5; SCCRO5
Summary: Enables cullin family protein binding activity. Involved in cellular response to DNA damage stimulus; positive regulation of protein neddylation; and regulation of cell growth. Located in nucleus and spindle. [provided by Alliance of Genome Resources, Apr 2022]
Expression: Ubiquitous expression in brain (RPKM 3.6), fat (RPKM 1.6) and 25 other tissues
Orthologs: mouse
Gene size: 41475bp
Exon count: 8