DLX2 and MSX1

  • Number of citations of the paper that reports this interaction (PMID 9111364)
  • 61
  • Data Source:
  • BioGRID (two hybrid)

DLX2

MSX1

Gene Name distal-less 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 14 interactors: AVP BZRAP1 DGCR6 DIP2A DLX5 GRN HOXC8 MSX1 MSX2 MVP NCOA2 PARK2 PIK3R1 XRCC6 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 1746 4487
HPRD ID 00527 00866
Ensembl ID ENSG00000115844 ENSG00000163132
Uniprot IDs Q07687 Q53QU7 P28360
PDB IDs
Enriched GO Terms of Interacting Partners?
Tagcloud ?
acquiring  adopt  ascl1  assemble  bhlh  combinatorial  derepression  derivative  diencephalic  discrete  dlx5  dlxs  helt  interneurons  nuclei  prethalamic  prethalamus  progenitor  relaying  rostral  spatiotemporal  specification  specified  surprisingly  th  thalamic  thalamus  tracing  whereby 
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) ?
acquiring  adopt  ascl1  assemble  bhlh  combinatorial  derepression  derivative  diencephalic  discrete  dlx5  dlxs  helt  interneurons  nuclei  prethalamic  prethalamus  progenitor  relaying  rostral  spatiotemporal  specification  specified  surprisingly  th  thalamic  thalamus  tracing  whereby 
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) ?