DCUN1D2 and CAND1

  • Number of citations of the paper that reports this interaction (PubMedID 26906416)
  • 9
  • Data Source:
  • BioGRID (affinity chromatography technology, affinity chromatography technology, pull down)

DCUN1D2

CAND1

Description defective in cullin neddylation 1 domain containing 2 cullin associated and neddylation dissociated 1
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GO Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
  • Amyotrophic lateral sclerosis (C9orf72 mutation interaction) ( 22959728)
  • Epstein-Barr virus copy number in lymphoblastoid cell lines ( 28654678)
  • Expressive vocabulary in infants ( 25226531)
  • Hippocampal atrophy ( 19668339)
  • Metabolite levels ( 23823483)
  • Systolic blood pressure ( 30224653)
Interacting Genes 7 interacting genes: APP CAND1 CUL2 CUL3 MAP3K1 UBE2F UBE2M 16 interacting genes: CA9 CNOT3 CUL1 CUL2 CUL3 CUL4A CUL4B DCUN1D1 DCUN1D2 DCUN1D4 DCUN1D5 MTNR1A RBX1 SKP1 SRPK2 UBE2M
Entrez ID 55208 55832
HPRD ID 12614 06983
Ensembl ID ENSG00000150401 ENSG00000111530
Uniprot IDs Q6PH85 Q86VP6
PDB IDs 4GAO 1U6G 4A0C
Enriched GO Terms of Interacting Partners?
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Tagcloud (Difference) ?
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