AGT and ITSN2

  • Number of citations of the paper that reports this interaction (PMID 22558309)
  • 5
  • Data Source:
  • BioGRID (two hybrid)

AGT

ITSN2

Gene Name angiotensinogen (serpin peptidase inhibitor, clade A, member 8) intersectin 2
Image
Gene Ontology Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
Protein-Protein Interactions 22 interactors: ACE2 AGTR1 AGTR2 ATP6AP2 CMA1 CTSG DNPEP ECE1 ENPEP EWSR1 GRB2 GSDMB ITSN2 KNG1 MAS1 MEP1A MME PRCP PREP PRG2 REN TP53 75 interactors: AGT AHDC1 AMPH ANKRD17 BCCIP CBL CCDC88C CHIC2 CPSF6 DLGAP1 DNM2 DST EPS15 EPS15L1 ERC1 FASLG FCHSD1 FCHSD2 FNBP4 GAREML GOLGA2 GOLGA8A GOLGB1 GPNMB HNRNPK HOOK2 ITPKA ITSN1 KCTD10 KDM1A KHDRBS1 KIAA1549 KXD1 LARP6 LSM8 LTBP4 LUC7L3 MAP4K3 MBNL1 MEGF10 NBR1 NR2C2 PDCD6IP PDE4DIP PIK3AP1 PIK3C2B PSEN1 PTN RABEP1 RAD9A RBMX REPS1 RNF20 ROCK1 RUFY1 SEMA6A SH3GL1 SH3KBP1 SNAP29 SOS1 SOS2 STX4 SYN1 SYNJ2 TACC1 TBL3 TMF1 TRIO WAS WASF2 WASL WIPF1 WIPF2 YLPM1 YTHDF1
Entrez ID 183 50618
HPRD ID 00106 09193
Ensembl ID ENSG00000135744 ENSG00000198399
Uniprot IDs B0ZBE2 B2R5S1 P01019 A6H8W8 Q9NZM3
PDB IDs 1N9U 1N9V 2JP8 2WXW 2X0B 4AA1 4APH 4FYS 1J3T 1UDL 1UE9 1UFF 1UHF 3GF9 3JZY
Enriched GO Terms of Interacting Partners?
Tagcloud ?
agc  alleles  amplified  autophosphorylation  berardinelli  changing  coding  codon  exons  heterozygous  iinsulin  inheritance  insulin  lesion  lipodystrophic  lipodystrophy  mellitus  outside  pathogenetic  polymorphism  polymorphisms  recessive  seip  sequenced  ser339  silent  substitution  unlikely  val 
abl1  adaptor  clathrin  colocalize  crk  domains  enabled  endocytosis  fgr  fyn  hela  interactors  interface  intersectin  isoform  isoforms  itsn1  itsns  mentioned  paralogous  pathologies  phospholipase  scaffolding  sh2  sh3  tyrosines  unable  vertebrates 
Tagcloud (Difference) ?
agc  alleles  amplified  autophosphorylation  berardinelli  changing  coding  codon  exons  heterozygous  iinsulin  inheritance  insulin  lesion  lipodystrophic  lipodystrophy  mellitus  outside  pathogenetic  polymorphism  polymorphisms  recessive  seip  sequenced  ser339  silent  substitution  unlikely  val 
abl1  adaptor  clathrin  colocalize  crk  domains  enabled  endocytosis  fgr  fyn  hela  interactors  interface  intersectin  isoform  isoforms  itsn1  itsns  mentioned  paralogous  pathologies  phospholipase  scaffolding  sh2  sh3  tyrosines  unable  vertebrates 
Tagcloud (Intersection) ?