Home News About DMDM Database Statistics Research Publications Contact  

 
Click for a Larger Image
  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


Tips:
 If you've navigated here from a protein, hovering over a position on the weblogo will display the corresponding protein position for that domain position.

 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 WcaG




















Weblogos are Copyright (c) 2002 Regents of the University of California




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.

   |   1000 Hilltop Circle, Baltimore, MD 21250   |   Department of Biological Sciences   |   Phone: 410-455-2258