DVL1 and NCK2

  • Number of citations of the paper that reports this interaction (PMID 25416956)
  • 0
  • Data Source:
  • BioGRID (two hybrid)

DVL1

NCK2

Gene Name dishevelled segment polarity protein 1 NCK adaptor protein 2
Image 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 80 interactors: ABI1 ABI2 ABI3 ARHGAP32 ATN1 AXIN1 AXL BCL11A CBLB CCDC33 CD3E CHN1 CPSF6 CPSF7 DDR1 DNM1 DOCK1 DOK1 DRAP1 DVL1 EEF1G EFHC2 EFNB1 EFNB2 EGFR EIF3H ERBB2 ERBB3 FAM53C FASLG FCRL2 FGFR1 FXR2 HNRNPK HOMEZ HOXC4 ILK IRS1 KHDRBS1 KIAA1217 LCP2 LIMS1 LNX1 LRRIQ3 LZTS2 MAGEA6 MASP1 MEOX2 NCKIPSD NPHS1 NR5A1 NTRK2 PAK1 PDGFRB PKN2 PRR20A PSMD10 PTK2 RASSF7 RBM26 REL SF3B4 SORBS2 SOS1 SPRY2 SRPK1 SRPK2 SYNPO TCF4 TNR TRIM27 TRIM41 TRIP6 VARS2 VPS37B WAS WASL WBP11 WIPF2 ZBTB7B
Entrez ID 1855 8440
HPRD ID 03220 05378
Ensembl ID ENSG00000107404 ENSG00000071051
Uniprot IDs O14640 Q86TH3 E7ERP6 O43639
PDB IDs 1U5S 1WX6 1Z3K 2B86 2CIA 2FRW 2FRY 2JXB 4E6R
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 
accumulates  adapter  atr  becoming  cleavage  coordination  cytoskeletal  depleted  depletion  discrete  hela  hyperactive  increasingly  interconnectedness  interconnectivity  irradiation  monitored  mostly  nck1  parp  phenocopies  redundant  shortly  socs7  strikingly  translocation  undergo  uv 
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 
accumulates  adapter  atr  becoming  cleavage  coordination  cytoskeletal  depleted  depletion  discrete  hela  hyperactive  increasingly  interconnectedness  interconnectivity  irradiation  monitored  mostly  nck1  parp  phenocopies  redundant  shortly  socs7  strikingly  translocation  undergo  uv 
Tagcloud (Intersection) ?