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  Domain Name: PMI_typeI
Phosphomannose isomerase type I. This is a family of Phosphomannose isomerase type I enzymes (EC 5.3.1.8).
No pairwise interactions found for the domain PMI_typeI

Total Mutations Found: 9
Total Disease Mutations Found: 9
This domain occurred 1 times on human genes (2 proteins).



  CONGENITAL DISORDER OF GLYCOSYLATION 1B (CDG1B)
  CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IB


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Range on the Protein:  

   Protein ID            Protein Position

Domain Position:  


No Conserved Features/Sites Found for PMI_typeI














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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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