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  Domain Name: Lectin_C
Lectin C-type domain. This family includes both long and short form C-type

Total Mutations Found: 102
Total Disease Mutations Found: 20
This domain occurred 77 times on human genes (161 proteins).



  3MC SYNDROME 2
  ASPERGILLOSIS, SUSCEPTIBILITY TO, INCLUDED
  BIRBECK GRANULE DEFICIENCY
  CANDIDIASIS, FAMILIAL, 4
  HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 6
  PULMONARY FIBROSIS, IDIOPATHIC
  PULMONARY FIBROSIS, IDIOPATHIC, SUSCEPTIBILITY TO
  SUSCEPTIBILITY TO LEPROSY AND MULTIBACILLARY LEPROSY


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 Lectin_C








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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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