PAX9 and MSX1

  • Number of citations of the paper that reports this interaction (PMID 16651263)
  • 23
  • Data Source:
  • HPRD (in vivo)

PAX9

MSX1

Gene Name paired box 9 msh homeobox 1
Image No pdb structure No pdb structure
Gene Ontology Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
  • Congenital heart disease ( 23708191)
  • Electrocardiographic conduction measures ( 19389651)
Protein-Protein Interactions 11 interactors: FUBP3 GTF2A1L KDM5B MSX1 NR0B2 SSX4 TLE1 TLE2 TRIP4 ZNF440 ZNF580 24 interactors: AES CREBBP DLX2 DLX5 HOXC8 ING4 LHX2 MED19 MSX2 NMNAT1 PAX3 PAX9 PIAS1 POU2F1 RGS7 SP1 SUMO1 SUMO2 TAF1 TBP TLE1 TLE2 TLE4 TP53
Entrez ID 5083 4487
HPRD ID 01336 00866
Ensembl ID ENSG00000198807 ENSG00000163132
Uniprot IDs P55771 Q2L4T1 P28360
PDB IDs
Enriched GO Terms of Interacting Partners?
Tagcloud ?
agenesis  c2c12  causative  clarify  convenient  electrophoretic  hard  homeodomain  hypodontia  illustrates  impair  l205r  lesser  leu205  leu205arg  mesenchymal  msx1  mutational  myod  nonsyndromic  oligodontia  oligonucleotide  pivotal  sampled  substitutions  t174i  thr174  thr174ile  tooth 
anomalies  cleft  clefts  cnv  cnvs  comprise  disrupting  doi  etiology  fgf8  foxe1  gli2  grouped  highlighting  irf6  jhg  journal  kif7  lip  mentioned  msx2  ofc  ofcs  orofacial  palate  postulated  satb2  ski  tceb3 
Tagcloud (Difference) ?
agenesis  c2c12  causative  clarify  convenient  electrophoretic  hard  homeodomain  hypodontia  illustrates  impair  l205r  lesser  leu205  leu205arg  mesenchymal  mutational  myod  nonsyndromic  oligodontia  oligonucleotide  pivotal  sampled  substitutions  t174i  thr174  thr174ile  tooth 
anomalies  cleft  clefts  cnv  cnvs  comprise  disrupting  doi  etiology  fgf8  foxe1  gli2  grouped  highlighting  irf6  jhg  journal  kif7  lip  mentioned  msx2  ofc  ofcs  orofacial  palate  postulated  satb2  ski  tceb3 
Tagcloud (Intersection) ?
msx1