首页> 外国专利> NEW GENE BEING IN DOMAIN IN WHICH CAUSATIVE GENE OF WERNER SYNDROME EXISTS, WS-2 AND PROTEIN CODED BY THE SAME GENE

NEW GENE BEING IN DOMAIN IN WHICH CAUSATIVE GENE OF WERNER SYNDROME EXISTS, WS-2 AND PROTEIN CODED BY THE SAME GENE

机译:Werner综合征的致病基因,WS-2和由相同基因编码的蛋白质中的新基因正在领域中

摘要

PROBLEM TO BE SOLVED: To obtain the subject new gene as a causative gene of Werner diseases useful for manufacturing a medicine for detecting the cause of a disease such as sterilitas and remitting the disease. ;SOLUTION: Gene WS-2 codes a polypeptide substantially containing an amino acid sequence of formula I or an amino acid sequence of formula II as its variant sequence. A coding map of a gene domain (WS domain) is formed by a position cloning method and detection of cDNA and determination of a base sequence is carried out by using a cloned PI/PAC DNA constituting the map to obtain a new gene WS-2.;COPYRIGHT: (C)1997,JPO
机译:解决的问题:获得作为Werner疾病的致病基因的主题新基因,该新基因可用于制造用于检测诸如雄性不育之类的疾病的病因并传播该疾病的药物。 ;解决方案:基因WS-2编码的多肽中基本上含有式I的氨基酸序列或式II的氨基酸序列作为其变异序列。通过位置克隆方法形成基因结构域(WS结构域)的编码图谱,检测cDNA,并使用构成该图谱的克隆的PI / PAC DNA进行碱基序列的确定,从而获得新的基因WS-2 。;版权:(C)1997,日本特许厅

著录项

  • 公开/公告号JPH09206080A

    专利类型

  • 公开/公告日1997-08-12

    原文格式PDF

  • 申请/专利权人 EIJIIN KENKYUSHO:KK;

    申请/专利号JP19960016236

  • 申请日1996-01-31

  • 分类号C12N15/09;A01K67/027;C07H21/04;C07K7/08;C07K14/47;C07K16/18;C12N1/21;C12N5/10;C12P21/02;C12P21/08;C12Q1/68;G01N33/53;G01N33/577;

  • 国家 JP

  • 入库时间 2022-08-22 03:37:36

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