SETD7 and NR2F2

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

SETD7

NR2F2

Gene Name SET domain containing (lysine methyltransferase) 7 nuclear receptor subfamily 2, group F, member 2
Image
Gene Ontology Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
  • Prostate cancer (gene x gene interaction) ( 22219177)
  • Response to TNF-alpha inhibitors in rheumatoid arthritis ( 22569225)
  • Sex hormone-binding globulin levels ( 22829776)
Protein-Protein Interactions 24 interactors: A1BG DNMT1 E2F1 ESR1 H3F3A HCFC1 HIST1H3A HIST1H4A HIST2H3C HIST3H3 KLF4 L3MBTL1 NR2F2 PPP1R12A PRKAR1A RELA SERTAD1 SIRT1 SOX2 STAT3 STEAP3 TAF10 TAF7 TP53 19 interactors: BCL11A BCL11B BIK EP300 FAM46A HDAC1 HIPK3 LCK MYOD1 NCOR2 NR2F6 NR3C1 NSD1 PHB2 PIAS1 SETD7 SQSTM1 TRIM24 TRIP4
Entrez ID 80854 7026
HPRD ID 16226 00139
Ensembl ID ENSG00000145391 ENSG00000185551
Uniprot IDs Q8WTS6 F1D8R0 P24468
PDB IDs 1H3I 1MT6 1MUF 1N6A 1N6C 1O9S 1XQH 2F69 3CBM 3CBO 3CBP 3M53 3M54 3M55 3M56 3M57 3M58 3M59 3M5A 3OS5 3VUZ 3VV0 4E47 4JDS 4JLG 3CJW
Enriched GO Terms of Interacting Partners?
Tagcloud ?
adenosylmethionine  biotinylated  broad  chemoproteomics  coactivator  cofactor  competition  competitive  confluent  derivative  druggable  enantiomer  exhibits  groove  hippo  kit  lysine  mcf7  methyltransferase  methyltransferases  occupying  pfi  phenocopied  pretreated  unusual  validate  valuable  yap  yes 
akr1c4  anomalies  apparently  array  balanced  bases  cdon  cgh  chrna7  confirming  dd  diagnoses  dock8  gata3  id  indistinguishable  inherited  intellectual  karyotype  karyotyping  mb  mca  overlooked  prenatal  pws  rearrangements  spanning  tier  tp63 
Tagcloud (Difference) ?
adenosylmethionine  biotinylated  broad  chemoproteomics  coactivator  cofactor  competition  competitive  confluent  derivative  druggable  enantiomer  exhibits  groove  hippo  kit  lysine  mcf7  methyltransferase  methyltransferases  occupying  pfi  phenocopied  pretreated  unusual  validate  valuable  yap  yes 
akr1c4  anomalies  apparently  array  balanced  bases  cdon  cgh  chrna7  confirming  dd  diagnoses  dock8  gata3  id  indistinguishable  inherited  intellectual  karyotype  karyotyping  mb  mca  overlooked  prenatal  pws  rearrangements  spanning  tier  tp63 
Tagcloud (Intersection) ?