COPB1 and FOXB1

  • Number of citations of the paper that reports this interaction (PMID 21988832)
  • 14
  • Data Source:
  • BioGRID (two hybrid)

COPB1

FOXB1

Gene Name coatomer protein complex, subunit beta 1 forkhead box B1
Image No pdb structure No pdb structure
Gene Ontology Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
Protein-Protein Interactions 32 interactors: ADAM19 APP ARCN1 ARF1 COPE COPG1 COPG2 ERBB2IP FOXB1 GRB2 HLA-DPB1 HLA-G ID1 IRAK3 KCNK3 KDELR1 LZTS2 NUB1 PDGFRB PRKCE RGS2 RGS4 RHOQ SERTAD1 SNTA1 TANK TAPBP TMED10 TRIM37 UBQLN4 VPS18 XRCC6 8 interactors: COPB1 KRT31 KRT40 KRTAP10-3 KRTAP10-8 NOTCH2NL PHF5A TRIM27
Entrez ID 1315 27023
HPRD ID 02981 07017
Ensembl ID ENSG00000129083 ENSG00000171956
Uniprot IDs P53618 Q99853
PDB IDs
Enriched GO Terms of Interacting Partners?
Tagcloud ?
ca037  ca530  cadd  chlamydiaceae  chlamydophila  copd1  copd2  inca  incc  pkn5  psittaci  scc1  scc2  scc3  sctc  sctd  sctj  sctl  sctn  sctq  sctr  scts  sctt  sctu  sctv  sctw  t3s  t3ss  tarp 
15q22  box  commonly  de  deletions  disability  documented  epilepsy  familial  forkhead  genotype  intellectual  kb  larger  mb  microdeletions  narg2  narrowed  neighboring  neurologic  neurological  novo  origin  orphan  par  phenotype  region  rora 
Tagcloud (Difference) ?
ca037  ca530  cadd  chlamydiaceae  chlamydophila  copd1  copd2  inca  incc  pkn5  psittaci  scc1  scc2  scc3  sctc  sctd  sctj  sctl  sctn  sctq  sctr  scts  sctt  sctu  sctv  sctw  t3s  t3ss  tarp 
15q22  box  commonly  de  deletions  disability  documented  epilepsy  familial  forkhead  genotype  intellectual  kb  larger  mb  microdeletions  narg2  narrowed  neighboring  neurologic  neurological  novo  origin  orphan  par  phenotype  region  rora 
Tagcloud (Intersection) ?