NME1 and RORA

  • Number of citations of the paper that reports this interaction (PMID 8858107)
  • 6
  • Data Source:
  • HPRD (in vitro, two hybrid)

NME1

RORA

Gene Name NME/NM23 nucleoside diphosphate kinase 1 RAR-related orphan receptor A
Image
Gene Ontology Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
Protein-Protein Interactions 27 interactors: APEX1 AURKA CCND3 FXR2 GORASP2 ITGB1 KSR1 MIF NIF3L1 NME2 NME3 NME4 PID1 POLR1C PRUNE RAC1 RORA RORB RRAD SET SMARCD1 SOX30 SREK1IP1 TERF1 TIAM1 TNPO2 WDYHV1 20 interactors: COPS5 EIF3I EP300 GFAP LMO3 LRIF1 MED1 MYOD1 NCOA1 NCOA2 NME1 NME2 NR0B1 NSD1 PNRC1 PNRC2 PROX1 PSMC5 SMARCD3 ZXDC
Entrez ID 4830 6095
HPRD ID 01131 02896
Ensembl ID ENSG00000239672 ENSG00000069667
Uniprot IDs P15531 F1DAL0 P35398
PDB IDs 1JXV 1UCN 2HVD 2HVE 3L7U 4ENO 1N83 1S0X
Enriched GO Terms of Interacting Partners?
Tagcloud ?
17q12  anonymous  brca1  cloning  colia1  d17s183  dinucleotide  edh17b  exclude  excludes  families  heterozygosity  hox2  inherited  locale  ngfr  nme2  ovarian  phb  pinpoint  polymorphisms  positional  q21  rara  recombination  resolving  scg43  thra1  wnt3 
15q21  backcross  cdna  chromosomal  chromosome  clone  fluorescence  hybridization  interspecific  map  mapped  member  mouse  partial  places  pml  promyelocytic  proximity  q22  rara  reciprocal  retinoid  situ  steroid  superfamily  thyroid  translocation  unique 
Tagcloud (Difference) ?
17q12  anonymous  brca1  cloning  colia1  d17s183  dinucleotide  edh17b  exclude  excludes  families  heterozygosity  hox2  inherited  locale  ngfr  nme2  ovarian  phb  pinpoint  polymorphisms  positional  q21  recombination  resolving  scg43  thra1  wnt3 
15q21  backcross  cdna  chromosomal  chromosome  clone  fluorescence  hybridization  interspecific  map  mapped  member  mouse  partial  places  pml  promyelocytic  proximity  q22  reciprocal  retinoid  situ  steroid  superfamily  thyroid  translocation  unique 
Tagcloud (Intersection) ?
rara