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  Domain Name: LRRCT
Leucine rich repeat C-terminal domain.
No pairwise interactions found for the domain LRRCT

Total Mutations Found: 21
Total Disease Mutations Found: 6
This domain occurred 85 times on human genes (145 proteins).



  HYPOGONADOTROPIC HYPOGONADISM 21 WITH ANOSMIA
  LEGIONNAIRE DISEASE, SUSCEPTIBILITY TO
  MACROTHROMBOCYTOPENIA, FAMILIAL, BERNARD-SOULIER TYPE
  NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1A
  VON WILLEBRAND DISEASE, PLATELET-TYPE


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Range on the Protein:  

   Protein ID            Protein Position

Domain Position:  


No Conserved Features/Sites Found for LRRCT






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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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