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  Domain Name: WNT1
found in Wnt-1.
No pairwise interactions found for the domain WNT1

Total Mutations Found: 33
Total Disease Mutations Found: 26
This domain occurred 19 times on human genes (33 proteins).



  FUHRMANN SYNDROME
  MULLERIAN APLASIA AND HYPERANDROGENISM
  ODONTOONYCHODERMAL DYSPLASIA
  OSTEOGENESIS IMPERFECTA, TYPE XV
  OSTEOPOROSIS, EARLY-ONSET, SUSCEPTIBILITY TO
  ROBINOW SYNDROME, AUTOSOMAL DOMINANT
  SCHOPF-SCHULZ-PASSARGE SYNDROME, INCLUDED;;
  SERKAL SYNDROME
  SPLIT-HAND/FOOT MALFORMATION 6
  TETRAAMELIA, AUTOSOMAL RECESSIVE
  TOOTH AGENESIS, SELECTIVE 4, INCLUDED
  TOOTH AGENESIS, SELECTIVE, 4
  TOOTH AGENESIS, SELECTIVE, 4, INCLUDED
  ULNA AND FIBULA, ABSENCE OF, WITH SEVERE LIMB DEFICIENCY


Tips:
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 The histograms below the weblogo indicate mutations found on the domain. Red is for disease (OMIM) and blue is for SNPs.

 Functional Features are displayed as orange boxes under the histograms. You can choose which features are displayed in the box below.



Range on the Protein:  

   Protein ID            Protein Position

Domain Position:  


No Conserved Features/Sites Found for WNT1















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Please Cite: Peterson, T.A., Adadey, A., Santana-Cruz ,I., Sun, Y., Winder A, Kann, M.G., (2010) DMDM: Domain Mapping of Disease Mutations. Bioinformatics 26 (19), 2458-2459.

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