FXR2 and NME1

  • Number of citations of the paper that reports this interaction (PMID 19060904)
  • 157
  • Data Source:
  • BioGRID (two hybrid)

FXR2

NME1

Gene Name fragile X mental retardation, autosomal homolog 2 NME/NM23 nucleoside diphosphate kinase 1
Image
Gene Ontology Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
Protein-Protein Interactions 90 interactors: AMOTL2 AP1M1 AP2M1 ARL6IP1 BAZ2B BRCA1 BYSL C10orf62 C1orf35 CALCOCO2 CAMK2D CBS CCDC33 CCDC85B CDKL3 CEP44 CEP55 COIL CYFIP1 CYFIP2 DPPA2 EWSR1 FAM90A1 FBP1 FMR1 FTH1 FXR1 GKAP1 HMBOX1 HNRNPC KCNRG KCTD4 KIAA1217 KIF1A KRT20 KXD1 LASP1 LCMT1 LCP2 LDOC1 MBIP MCRS1 MEAF6 MFAP1 MIA3 MORF4L1 MRPL43 NCK2 NDN NECAB2 NIF3L1 NME1 NONO NT5C2 PAF1 PAICS PCBD1 PIM1 POM121 PRAM1 PSME3 PTS RABAC1 RALYL RBBP8 RBMX RBPMS RPIA RTN3 RTN4 SCEL SNAP23 SRPK2 SSSCA1 SYT6 SYTL4 TBC1D22B THAP1 TNNT1 TRAF2 TRIM23 TRIM29 TRIM37 TSC22D4 YES1 ZBTB22 ZBTB8A ZMAT2 ZNF451 ZSCAN1 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
Entrez ID 9513 4830
HPRD ID 05629 01131
Ensembl ID ENSG00000129245 ENSG00000239672
Uniprot IDs P51116 P15531
PDB IDs 3H8Z 1JXV 1UCN 2HVD 2HVE 3L7U 4ENO
Enriched GO Terms of Interacting Partners?
Tagcloud ?
17p13  adipocytes  array  cgh  disability  duplication  dysmorphic  encodes  encompassing  facial  fingers  fissures  glut4  hyperpigmentation  intellectual  mandible  nlgn2  nostrils  obesity  p13  palpebral  proposita  recognizable  referred  seizures  slc2a4  slender  tp53  upturned 
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 
Tagcloud (Difference) ?
17p13  adipocytes  array  cgh  disability  duplication  dysmorphic  encodes  encompassing  facial  fingers  fissures  glut4  hyperpigmentation  intellectual  mandible  nlgn2  nostrils  obesity  p13  palpebral  proposita  recognizable  referred  seizures  slc2a4  slender  tp53  upturned 
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 
Tagcloud (Intersection) ?