NR0B2 and SMARCB1

  • Number of citations of the paper that reports this interaction (PMID 15314177)
  • 34

NR0B2

SMARCB1

Gene Name nuclear receptor subfamily 0, group B, member 2 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1
Image No pdb structure
Gene Ontology Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
Protein-Protein Interactions 46 interactors: AR CHRD DDX20 EID1 ESR1 ESR2 ESRRA ESRRG FN1 GPS2 HDAC3 HDAC6 HNF4A HNF4G HNRNPA1 IL3RA NCOA3 NR1H2 NR1H3 NR1I3 NR5A2 PAX9 PEF1 PLSCR1 POLR2A PPARD PPARG RARA RARG RBP5 RNF31 RXRA RXRB RXRG SMAD4 SMARCA2 SMARCB1 SMARCE1 SNW1 THRA TP53 UBC VDR XBP1 ZAP70 ZMYND10 40 interactors: AKT1 APP BCL2L11 CALR CDX2 CEBPB DPF2 DPF3 GADD45G GATA1 KLF1 KMT2B KMT2C MAP1LC3B MAPK8IP2 MCPH1 MECP2 MYC NONO NR0B2 NR3C1 PDPK1 PPP1CC PPP1R15A PRMT5 RAN RB1 RELB RPS6KA5 SIN3B SMARCA4 SRC TACC2 TAF1D TP53 UBQLN4 XPO1 YEATS4 ZAK ZDHHC17
Entrez ID 8431 6598
HPRD ID 05219 03364
Ensembl ID ENSG00000131910 ENSG00000099956
Uniprot IDs Q15466 G5E975 Q12824 Q9H836
PDB IDs 1YUC 2Q3Y 2Z4J 4DOR
Enriched GO Terms of Interacting Partners?
Tagcloud ?
abolished  adenovirus  ag490  amp  ataxia  atm  carboxykinase  gh  gluconeogenesis  hepatic  hepatocytes  heterodimer  interacted  ku  mediating  metformin  null  orphan  partner  pepck  phosphatidylinositol  phosphoenolpyruvate  physically  pivotal  regulating  shp  stat5  superfamily  telangiectasia 
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) ?
abolished  adenovirus  ag490  amp  ataxia  atm  carboxykinase  gh  gluconeogenesis  hepatic  hepatocytes  heterodimer  interacted  ku  mediating  metformin  null  orphan  partner  pepck  phosphatidylinositol  phosphoenolpyruvate  physically  pivotal  regulating  shp  stat5  superfamily  telangiectasia 
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) ?