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  Domain Name: LRR
Leucine-rich repeats, outliers.
No pairwise interactions found for the domain LRR

Total Mutations Found: 42
Total Disease Mutations Found: 16
This domain occurred 118 times on human genes (200 proteins).



  BERNARD-SOULIER SYNDROME, TYPE A1
  BERNARD-SOULIER SYNDROME, TYPE A2, AUTOSOMAL DOMINANT, INCLUDED
  BONE MINERAL DENSITY QUANTITATIVE TRAIT LOCUS 17
  DEAFNESS AND MYOPIA
  EPILEPSY, LATERAL TEMPORAL LOBE, AUTOSOMAL DOMINANT
  NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1A
  POLYCYSTIC KIDNEY DISEASE 1 (PKD1)


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Range on the Protein:  

   Protein ID            Protein Position

Domain Position:  


No Conserved Features/Sites Found for LRR





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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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