CDX2 and SMARCA4

  • Number of citations of the paper that reports this interaction (PMID 19371634)
  • 11

CDX2

SMARCA4

Gene Name caudal type homeobox 2 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4
Image No pdb structure
Gene Ontology Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
Protein-Protein Interactions 13 interactors: ACAT2 CDK2 CREBBP EP300 GSK3B HNF1A MAPK1 MAPK14 PAX6 SMARCA4 SMARCB1 SMARCD1 UBB 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
Entrez ID 1045 6597
HPRD ID 02622 04459
Ensembl ID ENSG00000127616
Uniprot IDs Q99626 A7E2E1 B3KNW7 P51532 Q9HBD4
PDB IDs 2GRC 2H60 3UVD
Enriched GO Terms of Interacting Partners?
Tagcloud ?
blastocyst  blastocysts  buffalo  caspase3  caspase6  caspase7  cleave  cleaving  cloning  competence  developmental  dnmt1  dnmt3a  ec  embryos  epigenetics  h3k27me3  h3k9ac  handmade  hdac1  hmc  ivf  lc  nanog  oct4  pluripotency  produced  sox2  trophectoderm 
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 
Tagcloud (Difference) ?
blastocyst  blastocysts  buffalo  caspase3  caspase6  caspase7  cleave  cleaving  cloning  competence  developmental  dnmt1  dnmt3a  ec  embryos  epigenetics  h3k27me3  h3k9ac  handmade  hdac1  hmc  ivf  lc  nanog  oct4  pluripotency  produced  sox2  trophectoderm 
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 
Tagcloud (Intersection) ?