INSRR and INSR

  • Number of citations of the paper that reports this interaction (PMID 8916919)
  • 2
  • Data Source:
  • HPRD (in vitro, in vivo)

INSRR

INSR

Gene Name insulin receptor-related receptor insulin receptor
Image No pdb structure
Gene Ontology Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
Protein-Protein Interactions 2 interactors: INSR KRT27 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
Entrez ID 3645 3643
HPRD ID 00976 00975
Ensembl ID ENSG00000027644 ENSG00000171105
Uniprot IDs P14616 P06213
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
Enriched GO Terms of Interacting Partners?
Tagcloud ?
aqpep  bcl2l11  clic6  dock1  en1  ephx3  fbxo17  fndc1  foxe1  foxl1  gbx2  gstm5  irx3  lbx2  loxl1  meis1  mt1h  nr2f2  parvg  phkg1  pitx1  pnliprp1  pou3f3  rasal  s1pr5  slc35d3  tbx4  tfap2c  xrn2 
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 
Tagcloud (Difference) ?
aqpep  bcl2l11  clic6  dock1  en1  ephx3  fbxo17  fndc1  foxe1  foxl1  gbx2  gstm5  irx3  lbx2  loxl1  meis1  mt1h  nr2f2  parvg  phkg1  pitx1  pnliprp1  pou3f3  rasal  s1pr5  slc35d3  tbx4  tfap2c  xrn2 
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 
Tagcloud (Intersection) ?