CCND1 and RBX1

  • Number of citations of the paper that reports this interaction (PMID 11311237)
  • 8
  • Data Source:
  • HPRD (in vivo)

CCND1

RBX1

Gene Name cyclin D1 ring-box 1, E3 ubiquitin protein ligase
Image
Gene Ontology Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
Protein-Protein Interactions 60 interactors: AKAP8 AR ARID4A ATF2 BRCA1 BRINP1 BTRC CALM1 CAMK1 CCNDBP1 CDK4 CDK6 CDKN1A CDKN1B CDKN1C CDKN2A CRYAB CTNNB1 CUL3 DMTF1 EP300 ESR1 FBXO31 FBXO4 GSK3B HDAC3 HERC5 IFI27 INSM1 KAT2B LPL MAPK11 MCM10 MCM7 MYBL2 NCOA1 NCOA3 NPDC1 ORC4 PCNA POLR1B PRKACA RABEP1 RB1 RBL1 RBL2 RBX1 RFC1 RUNX1 SP1 STAT3 TAF1 THRA THRB TP73 TSC2 UBTF UHRF2 USP2 XPO1 58 interactors: APP BRCA1 CAND1 CCND1 CCNE1 CDC34 COPS6 CSNK1E CTNNB1 CUL1 CUL3 CUL4A CUL4B CUL5 CUL7 DDB1 FBXO18 FBXW8 FRZB GLMN GPS1 HAX1 HIST1H1C MAP3K7 MAPK8IP2 MKNK2 MYB NFKBIA OS9 PLK1 PML PRAME RHOBTB3 RNF126 RPS6KB1 SAMHD1 SERTAD1 SKP1 SMAD3 TAB1 TP73 TRIM27 TRIM74 UBE2D1 UBE2D2 UBE2D3 UBE2E3 UBE2G1 UBE2G2 UBE2L3 UBE2L6 UBE2M UBE2R2 VHL VPRBP VRK2 WNK1 ZAK
Entrez ID 595 9978
HPRD ID 01346 06794
Ensembl ID ENSG00000110092
Uniprot IDs P24385 Q6FI00 P62877
PDB IDs 2W96 2W99 2W9F 2W9Z 1LDJ 1LDK 1U6G 2HYE 2LGV 3DPL 3DQV 3RTR 4F52
Enriched GO Terms of Interacting Partners?
Tagcloud ?
11q13  4nqo  7f4  amplicon  amplification  amplified  cavity  chr  distal  example  fgf3  fgf4  heterozygosity  hras1  inbred  inconsistently  involving  loh  murine  neck  nitroquinoline  portion  predispose  scc  strikingly  syntenic  telomeric  thirds  twofold 
adrenal  arise  bc  chromaffin  cnl  copy  cul2  disrupting  elongin  enrichment  harbored  heterozygosity  hif1  hif1a  hippel  hypoxic  indeed  inherited  lindau  merit  normoxic  pcc  pheochromocytomas  predisposing  pseudohypoxic  tceb1  tceb2  vhl  von 
Tagcloud (Difference) ?
11q13  4nqo  7f4  amplicon  amplification  amplified  cavity  chr  distal  example  fgf3  fgf4  hras1  inbred  inconsistently  involving  loh  murine  neck  nitroquinoline  portion  predispose  scc  strikingly  syntenic  telomeric  thirds  twofold 
adrenal  arise  bc  chromaffin  cnl  copy  cul2  disrupting  elongin  enrichment  harbored  hif1  hif1a  hippel  hypoxic  indeed  inherited  lindau  merit  normoxic  pcc  pheochromocytomas  predisposing  pseudohypoxic  tceb1  tceb2  vhl  von 
Tagcloud (Intersection) ?
heterozygosity