MYOD1 and NR2F2

  • Number of citations of the paper that reports this interaction (PMID 9826778)
  • 10
  • Data Source:
  • BioGRID (pull down)
  • HPRD (in vitro, in vivo)

MYOD1

NR2F2

Gene Name myogenic differentiation 1 nuclear receptor subfamily 2, group F, member 2
Image No pdb structure
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 61 interactors: ASCL3 BHLHA15 BHLHE40 BHLHE41 C2orf88 CALM1 CALM2 CALM3 CARM1 CDC34 CDK2 CDK4 CDKN1C CIB2 CREBBP CSRP3 ELSPBP1 EP300 HAND1 HDAC1 HEY1 HIST1H3A HSP90AA1 ID1 ID2 ID3 ID4 IFRD1 JUN KAT2B KAT5 KPNA3 MDFI MEF2A MEF2C MOS MYOCD NCOR1 NCOR2 NR2F2 PHB2 POLR2G PRKCA PRMT5 PSMD4 PSME2 RB1 RORA RUNX1 RXRA SETD3 SMAD3 SMAD4 SMAD7 SP1 SRF STAT3 SUV39H1 TCF3 TCF4 TWIST1 19 interactors: BCL11A BCL11B BIK EP300 FAM46A HDAC1 HIPK3 LCK MYOD1 NCOR2 NR2F6 NR3C1 NSD1 PHB2 PIAS1 SETD7 SQSTM1 TRIM24 TRIP4
Entrez ID 4654 7026
HPRD ID 01166 00139
Ensembl ID ENSG00000129152 ENSG00000185551
Uniprot IDs P15172 F1D8R0 P24468
PDB IDs 3CJW
Enriched GO Terms of Interacting Partners?
Tagcloud ?
antitrypsin  chn  chondrosarcoma  desmin  desmoplastic  ectomesenchymoma  etv1  ews  extraskeletal  fkhr  fli1  hhf35  liposarcoma  mic2  myxoid  p22  pax  pnet  q12  q14  q22  q24  q35  ssx1  stt  stts  syt  tec  witnessed 
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) ?
antitrypsin  chn  chondrosarcoma  desmin  desmoplastic  ectomesenchymoma  etv1  ews  extraskeletal  fkhr  fli1  hhf35  liposarcoma  mic2  myxoid  p22  pax  pnet  q12  q14  q22  q24  q35  ssx1  stt  stts  syt  tec  witnessed 
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) ?