SMARCA4 and CBX5

  • Number of citations of the paper that reports this interaction (PMID 12411497)
  • 28
  • Data Source:
  • HPRD (in vitro, in vivo, two hybrid)

SMARCA4

CBX5

Gene Name SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4 chromobox homolog 5
Image
Gene Ontology Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
Protein-Protein Interactions 73 interactors: ACTB ACTL6A AHR AR ARID1A ARID1B ARID2 BRCA1 BRWD1 CARM1 CBX5 CCNE1 CDK19 CDK8 CDKN2A CDX2 CEBPA CEBPB CHD4 CHMP5 CIITA CREB1 CTNNB1 DPF3 ESR1 ETS2 FANCA GATA1 GMNN H2AFX H3F3A HIST1H3A HIST1H4F HIST2H2BE HIST2H3C HSF1 HSF4 IKZF1 KLF1 MBD3 MDM2 MED17 MED6 MKL1 MPHOSPH6 MPP6 MYC MYOCD NR3C1 NR4A2 PABPN1 PAX6 PBRM1 PHB RAP1A RB1 RBL1 RBL2 RELB RFXAP SIN3A SIN3B SMARCB1 SMARCC1 SMARCE1 SS18 SS18L1 STAT2 STAT3 STK11 TMF1 TP53 ZMYND11 50 interactors: ARHGDIA ARL5A BCL11B CBX1 CBX3 CHAF1A DNMT3B DSN1 FSHR GOLGA8EP HDAC4 HDAC5 HDAC9 HIST1H1B HIST1H1E HIST2H3A HIST3H2A HIST3H2BB HIST3H3 HIST4H4 INCENP LBR LRIF1 MBD1 MCC MIS12 MKI67 NIPBL NR2F1 NSL1 PRR14 RPSA SMARCA4 SP1 SP100 SRPK1 SRPK2 STAM2 SUB1 SUV39H1 SUV39H2 TAF4 TCEB1 TCEB3B TRIM24 TRIM28 VPS28 WHSC1L1 XRCC6 XRN1
Entrez ID 6597 23468
HPRD ID 04459 05131
Ensembl ID ENSG00000127616 ENSG00000094916
Uniprot IDs A7E2E1 B3KNW7 P51532 Q9HBD4 P45973
PDB IDs 2GRC 2H60 3UVD 3FDT 3I3C
Enriched GO Terms of Interacting Partners?
Tagcloud ?
abnormality  arid1a  coinactivation  copyright  fish  frame  harboring  heterozygous  infancy  insights  malignancies  missense  monoploid  mrts  pbrm1  protected  remodeling  reserved  rhabdoid  rights  screened  sense  snf  subunits  swi  trisomy  truncating 
1alpha  aberrant  abstract  addressing  comprehensively  deregulation  di  diagnostics  dual  emerging  encoded  epigenetics  evolutionary  forming  h3k9me2  hallmark  heterochromatin  highlights  hp1alpha  mechanistic  metastasis  methylated  mitotic  networks  overview  serves  sight  therapeutics  tri 
Tagcloud (Difference) ?
abnormality  arid1a  coinactivation  copyright  fish  frame  harboring  heterozygous  infancy  insights  malignancies  missense  monoploid  mrts  pbrm1  protected  remodeling  reserved  rhabdoid  rights  screened  sense  snf  subunits  swi  trisomy  truncating 
1alpha  aberrant  abstract  addressing  comprehensively  deregulation  di  diagnostics  dual  emerging  encoded  epigenetics  evolutionary  forming  h3k9me2  hallmark  heterochromatin  highlights  hp1alpha  mechanistic  metastasis  methylated  mitotic  networks  overview  serves  sight  therapeutics  tri 
Tagcloud (Intersection) ?