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  Domain Name: JmjC
A domain family that is part of the cupin metalloenzyme superfamily. Probable enzymes, but of unknown functions, that regulate chromatin reorganisation processes (Clissold and Ponting, in press).
No pairwise interactions found for the domain JmjC

Total Mutations Found: 6
Total Disease Mutations Found: 3
This domain occurred 30 times on human genes (88 proteins).



  ALOPECIA UNIVERSALIS CONGENITA
  SIDERIUS X-LINKED MENTAL RETARDATION SYNDROME


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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 JmjC







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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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