RUNX1 and CCND1

  • Number of citations of the paper that reports this interaction (PMID 16287839)
  • 17
  • Data Source:
  • HPRD (in vivo)

RUNX1

CCND1

Gene Name runt-related transcription factor 1 cyclin D1
Image
Gene Ontology Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
Protein-Protein Interactions 46 interactors: AES AR CBFA2T2 CBFA2T3 CBFB CCND1 CCND2 CCND3 CDK1 CDK6 CEBPA CEBPB COPRS CTBP2 DNMT1 EFNA2 ELF2 ELF4 EP300 ETS1 FOS FOXP3 HDAC1 HDAC3 HIPK1 HIPK2 JUN KAT6A KAT6B MYOD1 NCOR1 NCOR2 PAX5 PRMT1 RBM14 SPEN STUB1 SUV39H1 TAZ TLE1 TLE2 UBE2L6 UXT VDR WWTR1 YAP1 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
Entrez ID 861 595
HPRD ID 01043 01346
Ensembl ID ENSG00000159216 ENSG00000110092
Uniprot IDs Q01196 P24385 Q6FI00
PDB IDs 1CMO 1CO1 1E50 1H9D 1LJM 2W96 2W99 2W9F 2W9Z
Enriched GO Terms of Interacting Partners?
Tagcloud ?
1q22  aml  correlative  cytogenetic  decitabine  demethylating  elucidate  epigenetics  frequent  haematological  hypermethylation  inactivation  inv  leukaemia  leukaemias  lymphocytic  malignancies  methylated  mostly  myelodysplatic  p13  promoters  re  relapse  runx2  runx3  syndromes  unmethylated 
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 
Tagcloud (Difference) ?
1q22  aml  correlative  cytogenetic  decitabine  demethylating  elucidate  epigenetics  frequent  haematological  hypermethylation  inactivation  inv  leukaemia  leukaemias  lymphocytic  malignancies  methylated  mostly  myelodysplatic  p13  promoters  re  relapse  runx2  runx3  syndromes  unmethylated 
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 
Tagcloud (Intersection) ?