DVL1 and ATN1

  • Number of citations of the paper that reports this interaction (PMID 10332026)
  • 8
  • Data Source:
  • BioGRID (two hybrid)

DVL1

ATN1

Gene Name dishevelled segment polarity protein 1 atrophin 1
Image No pdb structure No pdb structure
Gene Ontology Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
Protein-Protein Interactions 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 93 interactors: AES AGRN ALG13 ARF3 ATRX BAG6 BAIAP2 CACNB1 CASP1 CASP3 CBFA2T2 CENPJ CHRD CRACR2A CRIP2 CTNND2 DMPK DVL1 DVL2 ECM1 EFEMP1 EFEMP2 EWSR1 FBLN1 FBLN2 FBLN5 GAPDH GCC1 GIGYF1 GRN HINFP HSPG2 ITCH JAG2 KAT6A KAT6B KAT7 KRT31 KRTAP4-12 LENG8 LRP2 LTBP1 LTBP4 LYST MAGI1 MAGI2 MAP7D1 MBP MDFI MEGF11 MEGF6 MEGF8 NCK2 NELL1 NELL2 NOC2L NR2E1 PCSK5 PDCD6IP PFKL PLSCR1 PRRC2A PRRC2B PSMA3 PSME3 RAD54L2 RBFOX1 RBFOX2 RBM10 RBPMS RCHY1 RERE RHOXF2 RNF115 RNF31 RUNX1T1 SIAH1 SIAH2 SLIT1 SPAG5 SSPO STXBP4 SYVN1 TEP1 TLE1 TRIP6 USP54 VIM WDR5 WWP1 WWP2 ZMYND8 ZSWIM8
Entrez ID 1855 1822
HPRD ID 03220 06311
Ensembl ID ENSG00000107404 ENSG00000111676
Uniprot IDs O14640 Q86TH3 P54259 Q86V38
PDB IDs
Enriched GO Terms of Interacting Partners?
Tagcloud ?
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 
atrophin1  atrophy  chip  cortical  degenerative  demethylase  dentatorubral  depletion  h3k4  hint  inducing  knockout  lbal  lsd1  lysine  maintenance  methylation  npc  pallidoluysian  phenocopied  poorly  precise  premature  progenitor  repression  rescued  seq  surprisingly  tranylcypromine 
Tagcloud (Difference) ?
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 
atrophin1  atrophy  chip  cortical  degenerative  demethylase  dentatorubral  depletion  h3k4  hint  inducing  knockout  lbal  lsd1  lysine  maintenance  methylation  npc  pallidoluysian  phenocopied  poorly  precise  premature  progenitor  repression  rescued  seq  surprisingly  tranylcypromine 
Tagcloud (Intersection) ?