NR4A2 and SMARCA2

  • Number of citations of the paper that reports this interaction (PMID 17043312)
  • 26
  • Data Source:
  • BioGRID (affinity chromatography technology, pull down)

NR4A2

SMARCA2

Gene Name nuclear receptor subfamily 4, group A, member 2 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 2
Image
Gene Ontology Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
  • Autism spectrum disorder, attention deficit-hyperactivity disorder, bipolar disorder, major depressive disorder, and schizophrenia (combined) ( 23453885)
Protein-Protein Interactions 15 interactors: BAZ1B CDKN1C CDKN2D COPS5 PIAS4 PPARG RARA RARB RPS6KA1 RXRA RXRB SMARCA2 SMARCA4 TCEAL5 VHL 26 interactors: ACTL6A ACTL6B AR ARID1B BEND7 BRCA1 CEBPA DPF3 ESR1 HIST1H3A KHDRBS1 MDM2 MDM4 MECP2 MYB MYC NR0B2 NR3C1 NR4A2 PHB PITX1 PRMT5 PRPF6 SDCBP SIN3B SS18
Entrez ID 4929 6595
HPRD ID 03493 02483
Ensembl ID ENSG00000153234 ENSG00000080503
Uniprot IDs F1D8N6 F5H4G9 P43354 Q53EL4 Q6NXU0 P51531 Q56A76 Q8N9Q1
PDB IDs 1OVL 2DAT
Enriched GO Terms of Interacting Partners?
Tagcloud ?
519d  allograft  artificial  attenuate  bac  c19mc  cxcl6  decidua  evt  evts  extravillous  feto  foxl2  immunological  indirectly  invade  microrna  mirna  mirnas  myometrium  naturally  placenta  placental  trophoblast  trophoblasts  undifferentiated  utr  villous  vts 
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) ?
519d  allograft  artificial  attenuate  bac  c19mc  cxcl6  decidua  evt  evts  extravillous  feto  foxl2  immunological  indirectly  invade  microrna  mirna  mirnas  myometrium  naturally  placenta  placental  trophoblast  trophoblasts  undifferentiated  utr  villous  vts 
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) ?