CSNK1E and DVL1

  • Number of citations of the paper that reports this interaction (PMID 11818547)
  • 52
  • Data Source:
  • HPRD (in vivo, in vitro)

CSNK1E

DVL1

Gene Name casein kinase 1, epsilon dishevelled segment polarity protein 1
Image No pdb structure
Gene Ontology Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
Protein-Protein Interactions 40 interactors: AKAP9 ANKRD6 APC APP ARHGEF1 ARNTL AXIN1 AXIN2 BBS10 BID C2orf44 CADM4 CRY1 DVL1 DVL2 DVL3 FAM110A FAM110C FAM83D FBP1 GTF3C1 HES1 KAT7 MCC NCOA3 PER1 PER2 PER3 PNO1 PPP1CA PPP1R14A RAD54B RBX1 SDCCAG3 SOCS3 TAOK1 TAZ TNS2 ZMYND8 ZNF227 35 interactors: ANXA7 ARRB1 ATN1 AXIN1 BRD7 CCDC88C CSNK1D CSNK1E CSNK2A1 CTNNB1 CXXC4 DAAM1 DAB2 DVL3 DYNLT1 EPS8 FRAT1 HDHD2 HECW1 LRRK2 NCK2 NEDD4 PPM1A PSMA3 RAC1 SIPA1 SMAD1 SMAD2 SMAD3 SMAD4 SMAD7 TRIM69 USP13 VANGL1 VANGL2
Entrez ID 1454 1855
HPRD ID 02919 03220
Ensembl ID ENSG00000213923 ENSG00000107404
Uniprot IDs B0QY34 P49674 Q5U045 O14640 Q86TH3
PDB IDs 4HNI 4HOK
Enriched GO Terms of Interacting Partners?
Tagcloud ?
accessible  applicable  cancerous  chosen  constitute  crc  ctnnb1  hct  ihc  integrated  isogenic  kill  leave  lethality  msh2  pairs  polb  ranked  rb1  rko  rnai  sl  synergistically  therapeutics  top  tp53  uncovering  verified  wnt5a 
1p36  1q36  20p12  2q37  accumulating  boy  brachydactyly  chr1  chr2  chr20  cnv  cnvs  coarctation  deleted  deletion  digit  duplications  dysmorphism  facial  gpcpd1  hdac4  intellectual  malformations  p36  pcrs  phenotypes  simply  syndromic  tumorigenic 
Tagcloud (Difference) ?
accessible  applicable  cancerous  chosen  constitute  crc  ctnnb1  hct  ihc  integrated  isogenic  kill  leave  lethality  msh2  pairs  polb  ranked  rb1  rko  rnai  sl  synergistically  therapeutics  top  tp53  uncovering  verified  wnt5a 
1p36  1q36  20p12  2q37  accumulating  boy  brachydactyly  chr1  chr2  chr20  cnv  cnvs  coarctation  deleted  deletion  digit  duplications  dysmorphism  facial  gpcpd1  hdac4  intellectual  malformations  p36  pcrs  phenotypes  simply  syndromic  tumorigenic 
Tagcloud (Intersection) ?