ACVR2B and IGSF1

  • Number of citations of the paper that reports this interaction (PMID 11266516)
  • 5
  • Data Source:
  • BioGRID (affinity chromatography technology)
  • HPRD (in vivo)

ACVR2B

IGSF1

Gene Name activin A receptor, type IIB immunoglobulin superfamily, member 1
Image No pdb structure
Gene Ontology Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
Protein-Protein Interactions 18 interactors: ACVR1B BMP10 BMP2 BMP7 ERBB2IP GDF11 GDF2 GDF5 IGSF1 INHBA INHBB INHBC MSTN SNX1 SNX2 SNX6 SYNJ2BP TGFBRAP1 8 interactors: ACVR1 ACVR1B ACVR2A ACVR2B HECTD1 IGF1 INHBB RANBP10
Entrez ID 93 3547
HPRD ID 04106 02138
Ensembl ID ENSG00000114739 ENSG00000147255
Uniprot IDs Q13705 Q8N6C5
PDB IDs 2H62 2QLU 4FAO
Enriched GO Terms of Interacting Partners?
Tagcloud ?
arrays  bid  bmp2  bmpr1a  clustering  footprints  genechip  hybridized  infarct  ingenuity  ipa  ligation  lmna  mi  myocardial  myocardium  nfkbia  ninety  pathophysiological  porcine  probe  qrt  remodelling  remote  sacrificed  sets  smad1  tgfb3  tnfrsf1a 
boys  ch  congenital  definitive  exome  greatly  harbored  heterozygous  hypothyroidism  japanese  lacks  missense  mothers  nonsense  prolactin  q645x  r1189x  sequencing  severely  stature  superfamily  t3  t4  thereafter  thrive  traffic  unexplained  v1082e 
Tagcloud (Difference) ?
arrays  bid  bmp2  bmpr1a  clustering  footprints  genechip  hybridized  infarct  ingenuity  ipa  ligation  lmna  mi  myocardial  myocardium  nfkbia  ninety  pathophysiological  porcine  probe  qrt  remodelling  remote  sacrificed  sets  smad1  tgfb3  tnfrsf1a 
boys  ch  congenital  definitive  exome  greatly  harbored  heterozygous  hypothyroidism  japanese  lacks  missense  mothers  nonsense  prolactin  q645x  r1189x  sequencing  severely  stature  superfamily  t3  t4  thereafter  thrive  traffic  unexplained  v1082e 
Tagcloud (Intersection) ?