AHSG and INSR

  • Number of citations of the paper that reports this interaction (PMID 7906861)
  • 21
  • Data Source:
  • HPRD (in vivo)

AHSG

INSR

Gene Name alpha-2-HS-glycoprotein insulin receptor
Image No pdb structure
Gene Ontology Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
  • Activated partial thromboplastin time ( 22703881)
Protein-Protein Interactions 7 interactors: CDC42 DCN FBXO2 GRB2 INSR RRAS2 VKORC1 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 197 3643
HPRD ID 00727 00975
Ensembl ID ENSG00000145192 ENSG00000171105
Uniprot IDs P02765 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 ?
actual  african  americans  associations  caucasian  caucasians  causal  diabetes  directions  fasting  fetuin  genetically  glucose  incident  insignificant  mendelian  null  predicted  prevalent  proxies  raising  randomization  rs2248690  rs4917  sd  snps  trended  unbiased  variants 
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) ?
actual  african  americans  associations  caucasian  caucasians  causal  diabetes  directions  fasting  fetuin  genetically  glucose  incident  insignificant  mendelian  null  predicted  prevalent  proxies  raising  randomization  rs2248690  rs4917  sd  snps  trended  unbiased  variants 
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) ?