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Concurrency of Mutations, Microsatellites and Predicted Domains in kcnq1, kcnh2 and scn5a Genes Causing Long qt Syndrome Disease

DOI: 10.4172/jpb.s1000003

Keywords: Allam Appa Rao, G Venkata Swamy, B L V Vinay Kumar, Ch S U Ravi Kumar

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Abstract:

Bioinformatics is the field of science in which biology, computer science, and information technology merge to form a single discipline. The revolutionary growth in the computation speed and memory storage capability has fueled a new era in the analysis of biological data. The ultimate goal of the field is to enable the discovery of new biological insights as well as to create a global perspective from which unifying principles in biology can be discerned. Bioinformatics, also known as genomics, computational genomics, or computational molecular biology is a rate.We have used the analogy of genome analysis and VIRUS (vital information recourse under siege) and analyzed KCNQ1, KCNH2 and SCN5A genes, which are playing an important role in LQTS disease. We tried to find out whether the presence of microsatellites or simple sequence repeats in the KCNQ1, KCNH2 and SCN5A genes, are having any significance in the generation of these mutations and checked whether these mutations are fallen in the regions of those microsatillites and if so, is there any significance of these microsatillites in the functional domains of the each gene?.Our analysis revealed that 24 of the 26 mutations of the KCNQ1 gene, 19 of the 21 mutations of the KCNH2 gene and 3 of the 7 mutations of the SCN5A gene, which are existing in the microsatellite regions are fallen in the domain regions of the respective genes and thus indicating a positive role of microsatellites in mutagenesis

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