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  Domain Name: WcaG
Nucleoside-diphosphate-sugar epimerases [Cell envelope biogenesis, outer membrane / Carbohydrate transport and metabolism]
No pairwise interactions found for the domain WcaG

Total Mutations Found: 57
Total Disease Mutations Found: 43
This domain occurred 15 times on human genes (26 proteins).



  3-@BETA-HYDROXYSTEROID DEHYDROGENASE, TYPE II, DEFICIENCY OF
  ADRENAL HYPERPLASIA 2 (AH2)
  BILE ACID SYNTHESIS DEFECT, CONGENITAL, 1
  CHILD SYNDROME
  EPIMERASE-DEFICIENCY GALACTOSEMIA (EDG)
  GALACTOSE EPIMERASE DEFICIENCY
  GALACTOSE EPIMERASE DEFICIENCY, SEVERE
  LEIGH SYNDROME DUE TO MITOCHONDRIAL COMPLEX I DEFICIENCY


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Range on the Protein:  

   Protein ID            Protein Position

Domain Position:  


No Conserved Features/Sites Found for WcaG




















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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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