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  Domain Name: Chromo
Chromo (CHRromatin Organisation MOdifier) domain.
No pairwise interactions found for the domain Chromo

Total Mutations Found: 3
Total Disease Mutations Found: 2
This domain occurred 23 times on human genes (37 proteins).



  CHARGE SYNDROME
  EPILEPTIC ENCEPHALOPATHY, CHILDHOOD-ONSET
  HYPOGONADOTROPIC HYPOGONADISM 5 WITHOUT ANOSMIA, INCLUDED


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 The histograms below the weblogo indicate mutations found on the domain. Red is for disease (OMIM) and blue is for SNPs.

 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 Chromo







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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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