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  Domain Name: TPR_1
Tetratricopeptide repeat.

Total Mutations Found: 13
Total Disease Mutations Found: 5
This domain occurred 75 times on human genes (150 proteins).



  BARDET-BIEDL SYNDROME 4
  CILIARY DYSKINESIA, PRIMARY, 28, WITH SITUS INVERSUS
  GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME B-POSITIVE,
  TYPE II


Tips:
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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 TPR_1





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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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