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BRCA1 and BRCA2 germline mutations useful for predicting or detecting breast cancer or ovarian cancer

机译:BRCA1和BRCA2种系突变可用于预测或检测乳腺癌或卵巢癌

摘要

A BRCA1 and BRCA2 gene mutation is provided to detect breast cancer or ovarian cancer with low costs and high efficiency by providing the type of the mutation specific in Korean existing in the nucleotide sequential of BRCA1 and BRCA2. A polynucleotide consists of the 20-100 continuous nucleotide sequence. The 20-100 continuous nucleotide sequence includes a BRCA1 gene mutation selected from a group consisting of: the insertion of GGG and the deletion of AT in 38th base and 39th base in the polynucleotide consisting of the sequence of the sequence number 1; the substitution of 154th base from C to T in the polynucleotide consisting of the sequence of the sequence number 1; the substitution of 390th base from C to A in the polynucleotide consisting of the sequence of the sequence number 1; the substitution of 527th base from C to T in the polynucleotide consisting of the sequence of the sequence number 1; and the insertion of A between 720th base and 721th base in the polynucleotide consisting of the sequence of the sequence number.
机译:通过提供存在于BRCA1和BRCA2核苷酸序列中的朝鲜族特有突变类型,可以提供BRCA1和BRCA2基因突变,以低成本和高效率检测乳腺癌或卵巢癌。多核苷酸由20-100个连续核苷酸序列组成。 20-100个连续核苷酸序列包括BRCA1基因突变,该突变选自:由序列号1的序列组成的多核苷酸中GGG的插入和AT的第38和39个碱基的缺失;和在由序列号1的序列组成的多核苷酸中,将第154个碱基从C取代为T;在由序列号1的序列组成的多核苷酸中,第390个碱基从C取代为A;在由序列号1的序列组成的多核苷酸中,第527个碱基从C取代为T;并且在由序列号的序列组成的多核苷酸中的第720个碱基和第721个碱基之间插入A。

著录项

  • 公开/公告号KR100886937B1

    专利类型

  • 公开/公告日2009-03-09

    原文格式PDF

  • 申请/专利权人

    申请/专利号KR20070061088

  • 申请日2007-06-21

  • 分类号C12N15/10;C12N15/09;C12N15/12;C12Q1/68;

  • 国家 KR

  • 入库时间 2022-08-21 19:12:08

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