CCDC88C and DVL1

  • Number of citations of the paper that reports this interaction (PMID 14750955)
  • 4
  • Data Source:
  • HPRD (in vitro, in vivo, two hybrid)

CCDC88C

DVL1

Gene Name coiled-coil domain containing 88C dishevelled segment polarity protein 1
Image No pdb structure No pdb structure
Gene Ontology Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
Protein-Protein Interactions 5 interactors: APP DVL1 GNAI3 ITSN2 MAPK8 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 440193 1855
HPRD ID 19136 03220
Ensembl ID ENSG00000015133 ENSG00000107404
Uniprot IDs B4DZB8 Q9P219 O14640 Q86TH3
PDB IDs
Enriched GO Terms of Interacting Partners?
Tagcloud ?
ataxia  ataxias  atrophy  autosomal  causative  cerebellar  cerebellum  characterised  coil  coiled  congenital  cure  dominant  exhibits  exome  expands  g1391a  genetically  jnk  missense  neurological  pontocerebellar  r464h  sca  scas  spinocerebellar  triggers  unveils 
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) ?
ataxia  ataxias  atrophy  autosomal  causative  cerebellar  cerebellum  characterised  coil  coiled  congenital  cure  dominant  exhibits  exome  expands  g1391a  genetically  jnk  missense  neurological  pontocerebellar  r464h  sca  scas  spinocerebellar  triggers  unveils 
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) ?