LRP2 and APBB1

  • Number of citations of the paper that reports this interaction (PMID 9837937)
  • 99
  • Data Source:
  • HPRD (in vivo, two hybrid, in vitro)

LRP2

APBB1

Gene Name low density lipoprotein receptor-related protein 2 amyloid beta (A4) precursor protein-binding, family B, member 1 (Fe65)
Image
Gene Ontology Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
Protein-Protein Interactions 48 interactors: ALB ANAPC10 ANKRA2 ANKS1B APBA2 APBB1 APOB APOE APOH APP ATN1 CLU CUBN DAB1 DAB2 DLG1 DLG2 DLG3 DLG4 GC GIPC1 GPRASP1 INS ITGB1BP1 LCN2 LDLRAP1 LPA LPL LRP2BP LRPAP1 MAGI1 MAPK8IP1 MAPK8IP2 MDK NOS1AP PIP5K1C PLAU RBP1 SCGB1A1 SCN3A SERPINE1 SLC9A3 SNX17 SYNJ2BP TG THBS1 TLN1 TTR 66 interactors: ABI1 ABL1 ANXA1 APLP1 APLP2 APP ATXN1 ATXN1L CCDC97 CHERP CLSTN1 CPSF6 CPSF7 CYFIP1 CYFIP2 DDX17 DDX3X DDX46 DHX15 DHX9 DIAPH1 DIAPH2 EGFR ENAH ERBB2 EVL FASLG HNRNPH1 HNRNPK HTATSF1 KAT5 KHDRBS1 KHSRP LRP1 LRP2 NONO PABPC1 PQBP1 PRNP PTBP1 RBM17 RPL4 SF1 SF3A1 SF3A2 SF3A3 SF3B1 SF3B2 SF3B3 SF3B4 SFPQ TFCP2 THRAP3 TSHZ1 TSHZ2 TSHZ3 U2AF2 VASP WAS WASF2 WASL WBP11 WIPF1 WIPF2 YBX1 YLPM1
Entrez ID 4036 322
HPRD ID 02509 04087
Ensembl ID ENSG00000081479 ENSG00000166313
Uniprot IDs P98164 Q7Z5C0 Q7Z5C1 O00213
PDB IDs 2M0P 2E45 2HO2 2IDH 2OEI 3D8D 3D8E 3D8F 3DXC 3DXD 3DXE
Enriched GO Terms of Interacting Partners?
Tagcloud ?
adenosine  bioinformatics  ciliary  consequences  damaging  dnaaf1  eventual  exome  exploration  harbouring  heterozygote  hyperprolactinaemia  hypopituitarism  inexpensive  inosine  intriguing  itp  mendelian  morbid  novo  obesity  ontology  overrepresented  teenager  trios  triphosphate  ucp2  variants  wes 
a4  additive  aging  amyloid  apba3  aplp1  apolipoprotein  c57bl  clues  dysregulation  elusive  fe65  hippocampal  hypertension  hypertensive  impairments  m1  manifestation  maze  mint3  mo  muscarinic  object  precursor  predisposes  secretases  signature  tauopathy  wk 
Tagcloud (Difference) ?
adenosine  bioinformatics  ciliary  consequences  damaging  dnaaf1  eventual  exome  exploration  harbouring  heterozygote  hyperprolactinaemia  hypopituitarism  inexpensive  inosine  intriguing  itp  mendelian  morbid  novo  obesity  ontology  overrepresented  teenager  trios  triphosphate  ucp2  variants  wes 
a4  additive  aging  amyloid  apba3  aplp1  apolipoprotein  c57bl  clues  dysregulation  elusive  fe65  hippocampal  hypertension  hypertensive  impairments  m1  manifestation  maze  mint3  mo  muscarinic  object  precursor  predisposes  secretases  signature  tauopathy  wk 
Tagcloud (Intersection) ?