CCNB1 and RUNX2

  • Number of citations of the paper that reports this interaction (PMID 16407259)
  • 26
  • Data Source:
  • HPRD (in vivo)

CCNB1

RUNX2

Gene Name cyclin B1 runt-related transcription factor 2
Image No pdb structure
Gene Ontology Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
Protein-Protein Interactions 54 interactors: ANAPC11 ARID4A BRCA1 CCNB1IP1 CCNF CDC20 CDC25A CDC25C CDC27 CDC6 CDK1 CDK7 CDKN1A CDKN1B CDT1 CKS2 EP300 FLNA FZR1 GADD45A GADD45B GADD45G HERC5 HIST1H1A HIST1H1B ITPR1 KAT5 MAP4 MEF2C MOK PBK PCNA PIN1 PKMYT1 PLK1 POLA1 PRC1 PSMD4 PTCH1 PTMA RAD23A RALBP1 RB1 RPA1 RUNX2 SQSTM1 TGFBR2 TP53BP1 TP73 TSC1 TSPYL2 UBE2D2 UBE3D UBQLN1 36 interactors: ALYREF AR AXIN1 CBFB CCNB1 CDK1 CEBPB DVL2 EP300 ETS1 FHL2 FOS HDAC3 HDAC4 HDAC6 HIF1A HIVEP3 JUN KAT6B LEF1 MAP3K4 MSX2 PRKCD RB1 RBM14 SMAD2 SMAD3 SMAD6 SMURF2 SOX9 STUB1 TAF1A UBTF XRCC5 XRCC6 YAP1
Entrez ID 891 860
HPRD ID 00454 02566
Ensembl ID ENSG00000134057 ENSG00000124813
Uniprot IDs P14635 Q5TZP9 F8W8U5 Q13950 Q32MY8
PDB IDs 2B9R 2JGZ
Enriched GO Terms of Interacting Partners?
Tagcloud ?
5q13  bacs  bacterium  chosen  contig  copy  flanking  hope  inherited  intricate  legionella  lgn1  map1b  mapped  maps  muscular  naip  p1s  pathogenicity  pneumophila  recessively  simpler  sma  smas  smn  subcloning  syntenic  uncharacterized  yac 
1q22  aml  correlative  cytogenetic  decitabine  demethylating  elucidate  epigenetics  frequent  haematological  hypermethylation  inactivation  inv  leukaemia  leukaemias  lymphocytic  malignancies  methylated  mostly  myelodysplatic  p13  promoters  re  relapse  runx1  runx3  syndromes  unmethylated 
Tagcloud (Difference) ?
5q13  bacs  bacterium  chosen  contig  copy  flanking  hope  inherited  intricate  legionella  lgn1  map1b  mapped  maps  muscular  naip  p1s  pathogenicity  pneumophila  recessively  simpler  sma  smas  smn  subcloning  syntenic  uncharacterized  yac 
1q22  aml  correlative  cytogenetic  decitabine  demethylating  elucidate  epigenetics  frequent  haematological  hypermethylation  inactivation  inv  leukaemia  leukaemias  lymphocytic  malignancies  methylated  mostly  myelodysplatic  p13  promoters  re  relapse  runx1  runx3  syndromes  unmethylated 
Tagcloud (Intersection) ?