PSEN1 and CTNND2

  • Number of citations of the paper that reports this interaction (PMID 9223106)
  • 49
  • Data Source:
  • HPRD (in vitro, two hybrid, in vivo)

PSEN1

CTNND2

Gene Name presenilin 1 catenin (cadherin-associated protein), delta 2
Image No pdb structure
Gene Ontology Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
Protein-Protein Interactions 91 interactors: ACTN1 AP1M2 APBA1 APH1A APH1B APOE APP BACE1 BCL2 BCL2L1 CASP1 CASP3 CASP4 CASP6 CASP7 CASP8 CDH1 CDK5 CFL1 CIB1 CTNNA1 CTNNB1 CTNND1 CTNND2 CYP2C18 CYP2C8 DLL1 DOCK3 DSP ECSIT EFHD1 EFNB2 ENSA EPB41L3 ERN1 ETFA FBXL12 FBXW7 FGF13 FLNA FLNB GAPDH GCDH GDI1 GFAP GSK3B HERPUD1 HMGB1 ICAM5 ITSN2 JUP KANK2 KCNIP3 KCNIP4 MAPT METTL2B MTCH1 NCSTN NOS3 NOTCH1 NOTCH2 NOTCH3 NOTCH4 OXCT1 PDCD4 PIK3R1 PKP4 PRAM1 PRDX2 PRKACA PRKCZ PSENEN PSMA5 PSMB1 RAB11A RAB3A RAD23A RHEB RMDN3 RNF32 SCAF11 SCN1A ST13 STAMBPL1 TCF4 TCF7L2 TDP2 TUBA1B UBQLN1 UMPS YME1L1 18 interactors: ABL1 ATN1 CDH1 CDH2 CTNNB1 CTTN ERBB2IP FYN LCK LNX1 LRRC7 MAGI2 NUDT21 PDZD2 PSEN1 PSEN2 SPHK1 TTR
Entrez ID 5663 1501
HPRD ID 00087 09181
Ensembl ID ENSG00000080815 ENSG00000169862
Uniprot IDs P49768 B4DRK2 E7EPC8 Q9UQB3
PDB IDs 2KR6
Enriched GO Terms of Interacting Partners?
Tagcloud ?
1795g  2125g  abeta37  abeta39  abeta40  advance  dementia  dementias  doi  e599k  ejhg  fus  g709s  genetics  genotyping  granulin  grn  harbored  hek293  journal  lewy  mapt  neuropathological  pd  publically  publication  shifted  tar  variants 
16p11  17q21  2p21  acot7  autism  auts2  cask  categorised  cnvs  crebbp  delineating  exonic  grm8  homozygous  incidental  instrumental  iq  kb  med13l  microdeletion  morbid  ndds  neurodevelopmental  nrxn3  omim  pafah1b1  satb2  sizing  undiagnosed 
Tagcloud (Difference) ?
1795g  2125g  abeta37  abeta39  abeta40  advance  dementia  dementias  doi  e599k  ejhg  fus  g709s  genetics  genotyping  granulin  grn  harbored  hek293  journal  lewy  mapt  neuropathological  pd  publically  publication  shifted  tar  variants 
16p11  17q21  2p21  acot7  autism  auts2  cask  categorised  cnvs  crebbp  delineating  exonic  grm8  homozygous  incidental  instrumental  iq  kb  med13l  microdeletion  morbid  ndds  neurodevelopmental  nrxn3  omim  pafah1b1  satb2  sizing  undiagnosed 
Tagcloud (Intersection) ?