INSR and IGF2

  • Number of citations of the paper that reports this interaction (PMID 9722981)
  • 29
  • Data Source:
  • HPRD (in vivo)

INSR

IGF2

Gene Name insulin receptor insulin-like growth factor 2
Image
Gene Ontology Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
  • DNA methylation (variation) ( 23725790)
  • Femoral neck bone geometry and menarche (age at onset) ( 23593202)
  • Prostate cancer ( 19767753)
Protein-Protein Interactions 77 interactors: ACP1 ADRB2 AHSG ARF1 ARHGAP26 CALM1 CALM2 CALM3 CAV1 CAV3 CBL CEACAM1 CRK CRKL CSK DOK1 DOK4 DOK5 ENPP1 FABP4 FRS2 GAB1 GNB2L1 GRB10 GRB14 GRB7 HRAS IGF1R IGF2 INS INSRR IRF7 IRS1 IRS2 JAK1 JAK2 KHDRBS1 KRT27 KRT31 MAD2L1 MAPK3 PIK3R1 PIK3R3 PLCG1 PRKCA PRKCD PTK2 PTPN1 PTPN11 PTPN12 PTPN2 PTPN6 PTPRC PTPRF RAF1 RASA1 SH2B1 SH2B2 SHC1 SMAD2 SNX1 SNX2 SNX4 SNX6 SOCS1 SOCS2 SOCS3 SOCS6 SORBS1 SRC STAT5A STAT5B SYNCRIP TEAD1 VAV1 VAV3 YWHAB 22 interactors: BAG6 FAF1 GPC3 IDE IGF1R IGF2R IGFBP1 IGFBP2 IGFBP3 IGFBP4 IGFBP5 IGFBP6 IGFBP7 INSR NMRK2 NOV PCSK4 PLG RBPMS TF VTN WISP2
Entrez ID 3643 3481
HPRD ID 00975 00939
Ensembl ID ENSG00000171105 ENSG00000167244
Uniprot IDs P06213 P01344
PDB IDs 1GAG 1I44 1IR3 1IRK 1P14 1RQQ 2AUH 2B4S 2DTG 2HR7 2Z8C 3BU3 3BU5 3BU6 3EKK 3EKN 3ETA 3LOH 3W11 3W12 3W13 3W14 4IBM 1GF2 1IGL 2L29 2V5P 3E4Z 3KR3
Enriched GO Terms of Interacting Partners?
Tagcloud ?
birthweight  cognate  curly  delays  determinant  dwarfing  edema  eliminated  embryogenesis  embryos  epidermis  generalized  hypoplasia  igf1r  igf2  igr1r  indistinguishable  manifested  mildly  muscles  nullizygotes  nullizygous  ossification  phenotypically  recognizes  retardation  solely  thin  xr 
affects  biological  blast  carrying  cdna  cecum  crossed  deleted  disrupted  excess  exclusively  igf2r  involve  mannose  must  organ  organs  overexpressing  paternal  phenotypes  proteolytic  sdeltaigf2r  sigf2r  slow  solely  soluble  stomach  transgenics  transmembrane 
Tagcloud (Difference) ?
birthweight  cognate  curly  delays  determinant  dwarfing  edema  eliminated  embryogenesis  embryos  epidermis  generalized  hypoplasia  igf1r  igr1r  indistinguishable  manifested  mildly  muscles  nullizygotes  nullizygous  ossification  phenotypically  recognizes  retardation  thin  xr 
affects  biological  blast  carrying  cdna  cecum  crossed  deleted  disrupted  excess  exclusively  igf2r  involve  mannose  must  organ  organs  overexpressing  paternal  phenotypes  proteolytic  sdeltaigf2r  sigf2r  slow  soluble  stomach  transgenics  transmembrane 
Tagcloud (Intersection) ?
igf2  solely