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  Domain Name: COG3186
Phenylalanine-4-hydroxylase [Amino acid transport and metabolism]
No pairwise interactions found for the domain COG3186

Total Mutations Found: 56
Total Disease Mutations Found: 56
This domain occurred 4 times on human genes (9 proteins).



  ATTENTION DEFICIT-HYPERACTIVITY DISORDER, SUSCEPTIBILITY TO, 7
  BIPOLAR AFFECTIVE DISORDER, SUSCEPTIBILITY TO
  HYPERPHENYLALANINEMIA, NON-PKU
  HYPERPHENYLALANINEMIA, NON-PKU MILD
  PHENYLKETONURIA
  PHENYLKETONURIA, INCLUDED
  SEGAWA SYNDROME, AUTOSOMAL RECESSIVE
  UNIPOLAR DEPRESSION, SUSCEPTIBILITY TO


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Range on the Protein:  

   Protein ID            Protein Position

Domain Position:  


No Conserved Features/Sites Found for COG3186













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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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