IDENTIFICATION & SCREENING OF NSSNP’S FOR HYPERTHYROIDISM & PERFORMING MODELLING & DOCKING STUDIES ON NSSNP’S CODING PROTEIN OF HYPERTHYROIDISM
Jyothi J S, Anitha P M, Kusum Paul
Abstract
Hyperthyroidism, commonly known as overactive thyroid, occurs
mainly because of the presence of thyroid hormone in the bloodstream
in an abnormal way. The thyroid hormones are found in the thyroid
gland, which is located in the neck. Graves disease, Toxic thyroid
adenoma and Toxic Multi nodular goiter are some of the other reasons
causing hyperthyroidism. Hyperthyroidism is characterized by the
symptoms such as nervousness, irritability, increased perspiration,
hand tremors, anxiety and muscular weakness. Genetic variation and
Single nucleotide polymorphisms (SNPs) analysis will be an effective
approach to understand the molecular mechanism involved in
hyperthyroidism in an enhanced way. In our work, we identified
genetic variations followed by SNPs to investigate the genes involved in hyperthyroidism, so
as to obtain the target genes. The genetic variation and SNPs identification fetched us
C1QTNF6 as a target gene. There was need to find the structural information for C1QTNF6
genes, Modeller tool was used to serve this purpose. Finally, modelled structure was
validated, followed by docking studies to analyze interaction between target protein and lead
molecules.
Keywords: Hyperthyroidism, Genetic variation, non-synonymous SNPs.
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