LHX2 and MSX1

  • Number of citations of the paper that reports this interaction (PMID 9697309)
  • 10
  • Data Source:
  • HPRD (in vitro)

LHX2

MSX1

Gene Name LIM homeobox 2 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 5 interactors: CITED2 LDB1 MSX1 PAX6 RLIM 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 9355 4487
HPRD ID 04786 00866
Ensembl ID ENSG00000106689 ENSG00000163132
Uniprot IDs B3KNJ5 P50458 P28360
PDB IDs
Enriched GO Terms of Interacting Partners?
Tagcloud ?
ablated  conditionally  cuboid  delete  displaying  embryonically  ependymal  expresses  homeodomain  hypothalamic  intersectional  isl  lim  lin  mec  multiciliated  neuroepithelium  posteroventral  postnatally  radial  rarres2  rax  retaining  specification  specifying  sustaining  tanycyte  tanycytes  ultrastructural 
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) ?
ablated  conditionally  cuboid  delete  displaying  embryonically  ependymal  expresses  homeodomain  hypothalamic  intersectional  isl  lim  lin  mec  multiciliated  neuroepithelium  posteroventral  postnatally  radial  rarres2  rax  retaining  specification  specifying  sustaining  tanycyte  tanycytes  ultrastructural 
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) ?