NR0B2 and HNRNPA1

  • Number of citations of the paper that reports this interaction (PMID 21988832)
  • 14
  • Data Source:
  • BioGRID (two hybrid)

NR0B2

HNRNPA1

Gene Name nuclear receptor subfamily 0, group B, member 2 heterogeneous nuclear ribonucleoprotein A1
Image
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 32 interactors: ABHD16A APP ERG FEN1 HIPK3 HIST3H3 HMGA1 HNRNPH3 KHSRP NFKBIA NR0B2 NR3C1 PABPN1 PHYHIP PPIL1 PRKDC PRMT1 PRMT2 PRMT3 PRRC2A RNF14 RPL21 SAFB SREK1 SRPK1 SUFU TFEC TNPO1 TRA2B TTF2 XRN1 YWHAQ
Entrez ID 8431 3178
HPRD ID 05219 01242
Ensembl ID ENSG00000131910 ENSG00000135486
Uniprot IDs Q15466 P09651
PDB IDs 1YUC 2Q3Y 2Z4J 4DOR 1HA1 1L3K 1PGZ 1PO6 1U1K 1U1L 1U1M 1U1N 1U1O 1U1P 1U1Q 1U1R 1UP1 2H4M 2LYV 2UP1
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 
amyotrophic  autosomal  carriers  coding  conserved  equivocal  et  ewsr1  exons  export  familial  frontotemporal  fus  genotyped  genotyping  lobar  nes  neurodegeneration  pathogenicity  r471c  relatives  sequenced  subject  substitution  taf15  tardbp  tdp43  tremor 
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 
amyotrophic  autosomal  carriers  coding  conserved  equivocal  et  ewsr1  exons  export  familial  frontotemporal  fus  genotyped  genotyping  lobar  nes  neurodegeneration  pathogenicity  r471c  relatives  sequenced  subject  substitution  taf15  tardbp  tdp43  tremor 
Tagcloud (Intersection) ?