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  Domain Name: DCX
Domain in the Doublecortin (DCX) gene product. Tandemly-repeated domain in doublin, the Doublecortin gene product. Proposed to bind tubulin. Doublecortin (DCX) is mutated in human X-linked neuronal migration defects.
No pairwise interactions found for the domain DCX

Total Mutations Found: 49
Total Disease Mutations Found: 8
This domain occurred 9 times on human genes (20 proteins).



  LISSENCEPHALY, X-LINKED, 1
  OCCULT MACULAR DYSTROPHY (OCMD)
  OCCULT MACULAR DYSTROPHY, SUSCEPTIBILITY TO
  SUBCORTICAL LAMINAR HETEROTOPIA, X-LINKED, INCLUDED


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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 DCX







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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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