Home News About DMDM Database Statistics Research Publications Contact  

 
  Domain Name: S_TK_X
Extension to Ser/Thr-type protein kinases.
No pairwise interactions found for the domain S_TK_X

Total Mutations Found: 11
Total Disease Mutations Found: 4
This domain occurred 45 times on human genes (111 proteins).



  COWDEN DISEASE 6
  MEGALENCEPHALY-POLYMICROGYRIA-POLYDACTYLY-HYDROCEPHALUS SYNDROME
  MENTAL RETARDATION, X-LINKED 19
  SPINOCEREBELLAR ATAXIA 14


Tips:
 If you've navigated here from a protein, hovering over a position on the weblogo will display the corresponding protein position for that domain position.

 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 S_TK_X








Weblogos are Copyright (c) 2002 Regents of the University of California




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.

   |   1000 Hilltop Circle, Baltimore, MD 21250   |   Department of Biological Sciences   |   Phone: 410-455-2258