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HGVTB: a comprehensive online resource on human genes and genetic variants associated with tuberculosis

机译:HGV&TB:有关结核病的人类基因和遗传变异的综合在线资源

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摘要

Tuberculosis (TB) is an infectious disease caused by fastidious pathogen Mycobacterium tuberculosis. TB has emerged as one of the major causes of mortality in the developing world. Role of host genetic factors that modulate disease susceptibility have not been studied widely. Recent studies have reported few genetic loci that provide impetus to this area of research. The availability of tools has enabled genome-wide scans for disease susceptibility loci associated with infectious diseases. Till now, information on human genetic variations and their associated genes that modulate TB susceptibility have not been systematically compiled. In this work, we have created a resource: HGV&TB, which hosts genetic variations reported to be associated with TB susceptibility in humans. It currently houses information on 307 variations in 98 genes. In total, 101 of these variations are exonic, whereas 78 fall in intronic regions. We also analysed the pathogenicity of the genetic variations, their phenotypic consequences and ethnic origin. Using various computational analyses, 30 variations of the 101 exonic variations were predicted to be pathogenic. The resource is freely available at . Using integrative analysis, we have shown that the disease associated variants are selectively enriched in the immune signalling pathways which are crucial in the pathophysiology of TB. >Database URL:
机译:结核病(TB)是由病原体结核分枝杆菌引起的传染病。结核病已成为发展中国家死亡的主要原因之一。宿主遗传因素调节疾病易感性的作用尚未得到广泛研究。最近的研究报道很少有基因位点可以推动这一领域的研究。工具的可用性使对与传染病相关的疾病易感基因座进行全基因组扫描。到目前为止,有关人类遗传变异及其调节结核易感性的相关基因的信息尚未得到系统地汇编。在这项工作中,我们创建了一个资源:HGV&TB,该基因承载着与人类结核病易感性相关的遗传变异。它目前包含有关98个基因的307个变异的信息。总体而言,这些变异中有101个是外显子,而78个落入内含子区域。我们还分析了遗传变异的致病性,它们的表型后果和种族血统。使用各种计算分析,预测101种外显子变异中的30种变异是致病的。该资源可从以下网址免费获得。使用综合分析,我们已经表明,与疾病相关的变异体选择性地丰富了在结核病病理生理中至关重要的免疫信号通路。 >数据库网址:

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