首页> 外国专利> UGT1A6 GENE SNP MARKERS ASSOCIATED WITH SERUM BILIRUBIN CONCENTRATION AND USES THEREOF

UGT1A6 GENE SNP MARKERS ASSOCIATED WITH SERUM BILIRUBIN CONCENTRATION AND USES THEREOF

机译:与血清胆红素浓度有关的UGT1A6基因SNP标记及其用途

摘要

PURPOSE: A kit for predicting blood bilirubin concentration of a test sample and a method for detecting a bilirubin marker are provided to easily diagnose hyperbilirubinemia. CONSTITUTION: A kit for predicting blood bilirubin concentration of a test sample contains: 8-100 sequential nucleotide sequences having single nucleotide polymorphism(SNP) positioned at 301th nucleotide of sequence number 1-4, 8-11 and 13, 314th nucleotide of sequence number 5, 201th nucleotide of sequence number 6, 234th nucleotide of sequence number 7, 308th nucleotide of sequence number 12, 307th nucleotide of sequence number 14, and 136th nucleotide of sequence number 15; and a complementary nucleotide thereof. The prediction of bilirubin concentration is used for diagnosing hyperbilirubinemia, jaundice, Gilbert syndrome, Dubin-Johnson syndrome, Rotor syndrome, or Crigler-najjar syndrome.
机译:目的:提供一种用于预测测试样品的血液胆红素浓度的试剂盒和一种检测胆红素标记的方法,以轻松诊断高胆红素血症。构成:一种用于预测测试样品的血液胆红素浓度的试剂盒,其包含:8-100个具有单核苷酸多态性(SNP)的连续核苷酸序列,分别位于序列号1-4、8-11和13的第301个核苷酸,序列号的第314个核苷酸5,序列号6的201个核苷酸,序列号7的234个核苷酸,序列号12的308个核苷酸,序列号14的307个核苷酸,序列号15的136个核苷酸;及其互补核苷酸。胆红素浓度的预测可用于诊断高胆红素血症,黄疸,吉尔伯特综合征,杜宾-约翰逊综合征,转子综合征或Crigler-najjar综合征。

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