HOXC8 and MSX1

  • Number of citations of the paper that reports this interaction (PMID 9111364)
  • 61

HOXC8

MSX1

Gene Name homeobox C8 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: BMPR1A BTG2 DLX2 DLX5 GMNN HOMEZ JUN MSX1 SMAD1 SMAD4 SMAD6 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 3224 4487
HPRD ID 00856 00866
Ensembl ID ENSG00000163132
Uniprot IDs P31273 P28360
PDB IDs
Enriched GO Terms of Interacting Partners?
Tagcloud ?
abrogates  cdkn1b  correlates  cyclophilin33  cyp33  downregulation  h3k4me3  h4  homeodomain  hoxa9  implying  isomerase  lineage  lost  mediates  mll  mutually  phd3  preferentially  proline  reinsertion  repression  rrm  selectivity  structurally  switch  transforming  translocations  trimethylated 
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) ?
abrogates  cdkn1b  correlates  cyclophilin33  cyp33  downregulation  h3k4me3  h4  homeodomain  hoxa9  implying  isomerase  lineage  lost  mediates  mll  mutually  phd3  preferentially  proline  reinsertion  repression  rrm  selectivity  structurally  switch  transforming  translocations  trimethylated 
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) ?