APBB1 and CYFIP2

  • Number of citations of the paper that reports this interaction (PMID 16055720)
  • 52

APBB1

CYFIP2

Gene Name amyloid beta (A4) precursor protein-binding, family B, member 1 (Fe65) cytoplasmic FMR1 interacting protein 2
Image No pdb structure
Gene Ontology Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
Protein-Protein Interactions 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 20 interactors: ABI1 ABI3 APBB1 BIRC3 BRK1 DNMBP FMR1 FXR1 FXR2 GAS7 NCK1 NCKAP1 PLG PRPF40A SMAD4 TCERG1 WASF1 WASF2 YWHAG ZC3H12A
Entrez ID 322 26999
HPRD ID 04087 07556
Ensembl ID ENSG00000166313 ENSG00000055163
Uniprot IDs O00213 E7EVJ5 E7EW33 F5H583 Q96F07
PDB IDs 2E45 2HO2 2IDH 2OEI 3D8D 3D8E 3D8F 3DXC 3DXD 3DXE
Enriched GO Terms of Interacting Partners?
Tagcloud ?
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 
als  amyotrophic  beacons  biomarkers  creating  discovered  etiology  fals  familial  fatal  g93a  hmsc  inherited  leukocyte  msod1  ones  path  pathogenetic  pave  rbbp9  sals  secretory  share  signature  slpi  sod1  spatiotemporal  sporadic  tar 
Tagcloud (Difference) ?
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  tauopathy  wk 
als  amyotrophic  beacons  biomarkers  creating  discovered  etiology  fals  familial  fatal  g93a  hmsc  inherited  leukocyte  msod1  ones  path  pathogenetic  pave  rbbp9  sals  secretory  share  slpi  sod1  spatiotemporal  sporadic  tar 
Tagcloud (Intersection) ?
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