PSEN1 and CYP2C8

  • Number of citations of the paper that reports this interaction (PMID 21163940)
  • 13
  • Data Source:
  • BioGRID (two hybrid)

PSEN1

CYP2C8

Gene Name presenilin 1 cytochrome P450, family 2, subfamily C, polypeptide 8
Image
Gene Ontology Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
  • Immune response to smallpox vaccine (IL-6) ( 22542470)
  • Osteonecrosis of the jaw ( 18594024)
  • Response to clopidogrel therapy ( 19706858)
  • Warfarin maintenance dose ( 23755828)
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 11 interactors: A2M APOE BLMH DNAJB1 ECSIT EXOC6 IFIT3 LONP1 MAST1 PSEN1 RNF32
Entrez ID 5663 1558
HPRD ID 00087 03083
Ensembl ID ENSG00000080815 ENSG00000138115
Uniprot IDs P49768 B7Z1F5 P10632
PDB IDs 2KR6 1PQ2 2NNH 2NNI 2NNJ 2VN0
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 
allele  apolipoprotein  associations  cardiotoxicity  commonly  comt  conform  epsilon4  failed  fatigue  genetic  genotype  guidelines  il6  impairment  listed  lle655val  met  neuropathy  polymorphisms  reporting  strega  systematic  toxicities  transparent  underlying  val  variant  variants 
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 
allele  apolipoprotein  associations  cardiotoxicity  commonly  comt  conform  epsilon4  failed  fatigue  genetic  genotype  guidelines  il6  impairment  listed  lle655val  met  neuropathy  polymorphisms  reporting  strega  systematic  toxicities  transparent  underlying  val  variant 
Tagcloud (Intersection) ?
variants