ACVR1B and IGSF1

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

ACVR1B

IGSF1

Gene Name activin A receptor, type IB immunoglobulin superfamily, member 1
Image No pdb structure No pdb structure
Gene Ontology Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
Protein-Protein Interactions 20 interactors: ACVR2B BAG6 BAMBI BMPR2 FKBP1A IGSF1 INHBA INHBB INHBC NEDD4L OS9 PRKACB RXRA SMAD2 SMAD4 SMAD7 SNX1 SNX2 TDGF1 TGFBRAP1 8 interactors: ACVR1 ACVR1B ACVR2A ACVR2B HECTD1 IGF1 INHBB RANBP10
Entrez ID 91 3547
HPRD ID 03193 02138
Ensembl ID ENSG00000135503 ENSG00000147255
Uniprot IDs P36896 Q8N6C5
PDB IDs
Enriched GO Terms of Interacting Partners?
Tagcloud ?
125b  acvr2a  arid3b  bak1  bcl2l2  bear  bim  bmpr1b  cadm1  cardio  cardiology  cmass  e2f3  fgfr2  fgfr3  glut3  il6r  jph2  men1  mirs  onco  orchestration  raf1  sitr7  smoothened  st7l  twist1  wee1  wnt7a 
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) ?
125b  acvr2a  arid3b  bak1  bcl2l2  bear  bim  bmpr1b  cadm1  cardio  cardiology  cmass  e2f3  fgfr2  fgfr3  glut3  il6r  jph2  men1  mirs  onco  orchestration  raf1  sitr7  smoothened  st7l  twist1  wee1  wnt7a 
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) ?