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Method for predicting susceptibility to cardiovascular disease using SNP of klotho genes

机译:用klotho基因的SNP预测心血管疾病易感性的方法

摘要

PURPOSE: A cardiovascular disease prediction method using the single nucleotide polymorphism of Klotho gene is provided to be practically used for the prevention and the early diagnosis of the cardio vascular disease as it verifies genetic factors which causes cardiovascular disease. CONSTITUTION: A marker for prediction of the degree of the cardiovascular disease outbreak danger is selected from rs3631726 with the base rank in a rank number 3 and composed of a polynucleotide or a supplementary polynucleotide thereof with 20-100 continuous DNA rank in which 27th base (744th base from the transcription starting point of the klotho gene) is A or lacked. The cardiovascular disease is selected from the myocardial infarction, angina, atherosclerosis, hypertension, cardiac failure, blood tumor, artery scleroma, embolism, stroke and thrombosis. A probe or a primer is included which can detect the cardiovascular disease pathogenic risk marker for prediction. The kit is the RT-PCR kit or the DNA chip kit. Polynucleotide or its supplementary polynucleotide with 20-100 of continuous DNA rank is included that is selected from rs36217263 with the base rank of the rank number 3 and in which 27th base (744th base from the transcription starting point of the klotho gene) is A or lacked.
机译:目的:提供一种利用Klotho基因单核苷酸多态性预测心血管疾病的方法,因为它可以验证导致心血管疾病的遗传因素,因此可用于预防和早期诊断心血管疾病。组成:用于预测心血管疾病暴发危险程度的标志物选自rs3631726,其碱基排名在3位,由具有20-100个连续DNA等级的多核苷酸或其补充多核苷酸组成,其中第27个碱基(从klotho基因的转录起点算起第744个碱基为A或缺少。心血管疾病选自心肌梗塞,心绞痛,动脉粥样硬化,高血压,心力衰竭,血液肿瘤,动脉硬化,栓塞,中风和血栓形成。包括可以检测心血管疾病致病风险标记以进行预测的探针或引物。该试剂盒是RT-PCR试剂盒或DNA芯片试剂盒。包括具有连续DNA等级20-100的多核苷酸或其补充多核苷酸,其选自具有等级编号3的碱基等级的rs36217263,并且其中第27个碱基(从klotho基因的转录起始点起第744个碱基)是A或缺乏。

著录项

  • 公开/公告号KR101304535B1

    专利类型

  • 公开/公告日2013-09-09

    原文格式PDF

  • 申请/专利权人

    申请/专利号KR20110088722

  • 申请日2011-09-01

  • 分类号C12N15/11;C12Q1/68;

  • 国家 KR

  • 入库时间 2022-08-21 16:24:29

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