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SLCO2B1 Novel SLCO2B1 Single Nucleotide Polymorphism Markers and Uses Thereof

机译:SLCO2B1新型SLCO2B1单核苷酸多态性标记及其用途

摘要

The invention SLCO2B1 (Solute carrier organic anion transporter family member 2B1) the novel single nucleotide polymorphism present in the gene (single nucleotide polymorphism; SNP) and relates to the marker uses for its drug response prediction, and more particularly, SLCO2B1 polymorphism using drug response prediction or diagnostic composition, drug response prediction or diagnosis kit, method of providing information for drug selection decision, a method provides information for a single nucleotide polymorphism of a gene mutant genotype detection method and SLCO2B1 genes associated with drug response to will be. SLCO2B1 novel single nucleotide polymorphism marker presented in this invention may be useful as a biological marker associated with at least a drug transporter function. In other words, it is possible to use the novel SLCO2B1 polymorphism of the invention in a biological marker to predict or diagnose a symptom caused by differences of the sample and a drug transporter deficient individual drug transporter activity. In particular, SLCO2B1 genetic polymorphism of the present invention may contribute to the development of genetic diagnostics for Koreans by providing critical information in the development of Korean-based personalized drug therapies as a novel mutant gene discovery targeting Koreans.;
机译:SLCO2B1(溶质载体有机阴离子转运蛋白家族成员2B1)存在于基因中的新型单核苷酸多态性(单核苷酸多态性; SNP),并且涉及用于其药物应答预测的标志物用途,更具体地,涉及使用药物应答的SLCO2B1多态性预测或诊断组成,药物反应预测或诊断试剂盒,为药物选择决策提供信息的方法,为基因突变基因型检测方法的单核苷酸多态性和与药物反应相关的SLCO2B1基因提供信息的方法。本发明提出的SLCO2B1新型单核苷酸多态性标记物可用作与至少一种药物转运蛋白功能相关的生物标记物。换句话说,有可能在生物学标志物中使用本发明的新型SLCO2B1多态性,以预测或诊断由样品和药物转运蛋白缺乏的个体药物转运蛋白活性的差异引起的症状。特别地,本发明的SLCO2B1遗传多态性可通过在基于韩国人的个性化药物疗法的开发中提供关键信息作为针对韩国人的新型突变基因发现,来促进针对韩国人的遗传诊断的发展。

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