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  Domain Name: PX
PhoX homologous domain, present in p47phox and p40phox. Eukaryotic domain of unknown function present in phox proteins, PLD isoforms, a PI3K isoform.
No pairwise interactions found for the domain PX

Total Mutations Found: 20
Total Disease Mutations Found: 7
This domain occurred 46 times on human genes (91 proteins).



  FRANK-TER HAAR SYNDROME
  GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME B-POSITIVE,
  OSTEOPETROSIS, AUTOSOMAL RECESSIVE 8
  TYPE I
  TYPE III


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 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 PX














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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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