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  Domain Name: Aminotran_1_2
Aminotransferase class I and II.
No pairwise interactions found for the domain Aminotran_1_2

Total Mutations Found: 42
Total Disease Mutations Found: 35
This domain occurred 15 times on human genes (33 proteins).



  ANEMIA, HEREDITARY SIDEROBLASTIC
  ANEMIA, HEREDITARY SIDEROBLASTIC, LATE-ONSET
  ANEMIA, HEREDITARY SIDEROBLASTIC, PYRIDOXINE REFRACTORY
  NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IC, SEVERE
  NEUROPATHY, HEREDITARY SENSORY, TYPE IC
  TYROSINEMIA, TYPE II


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Range on the Protein:  

   Protein ID            Protein Position

Domain Position:  


No Conserved Features/Sites Found for Aminotran_1_2


















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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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