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  Domain Name: Transglut_N
Transglutaminase family.

Total Mutations Found: 27
Total Disease Mutations Found: 14
This domain occurred 9 times on human genes (12 proteins).



  FACTOR XIII, A SUBUNIT, DEFICIENCY OF
  ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 1
  ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 1, WITH BATHING SUIT DISTRIBUTION
  ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 1, WITH OR WITHOUT BATHING
  PEELING SKIN SYNDROME, ACRAL TYPE
  SPHEROCYTOSIS 5 (SPH5)
  SPHEROCYTOSIS, TYPE 5, DUE TO PROTEIN 4.2-NIPPON
  SPINOCEREBELLAR ATAXIA 35 (SCA35)
  SUIT DISTRIBUTION


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Range on the Protein:  

   Protein ID            Protein Position

Domain Position:  


No Conserved Features/Sites Found for Transglut_N









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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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