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Polymorphic analysis of the human phosphoglucomutase-3 gene based on mismatched PCR-RFLP technique.

机译:基于错配PCR-RFLP技术的人类磷酸葡萄糖突变酶3基因的多态性分析。

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Polymorphic analysis of human phosphoglucomutase-3 (PGM(3)) has been carried out from the level of the gene product. Due to a weak zymogram, leading to ambiguity in phenotyping, information on the PGM(3) locus has rarely been reported. In this study, the missense mutation G1396A, confirmed to underlie common phenotypes of PGM(3), was identified by performing mismatched PCR-RFLP. Population data on the PGM(3) locus was also obtained for the first time in China. The allele frequency distribution was PGM(3)*1 = 0.625, PGM(3)*2 = 0.375, and no deviation from Hardy-Weinberg equilibrium was observed. The application of the information in both genetics and forensic medicine demonstrated that the polymorphism information content was 0.5163, heterozygosity 0.4872, power of discrimination 0.5986, and probability of paternity exclusion 0.1794. Polymorphic analysis of the locus at the DNA level will also provide significant data for disease susceptibility and linkage analysis.
机译:从基因产物的水平进行了人类磷酸葡萄糖突变酶3(PGM(3))的多态性分析。由于弱的酶谱图,导致表型不明确,有关PGM(3)基因座的信息鲜有报道。在这项研究中,通过执行错配的PCR-RFLP鉴定了错义突变G1396A,证实其是PGM(3)常见表型的基础。在中国也首次获得了PGM(3)基因座的人口数据。等位基因频率分布为PGM(3)* 1 = 0.625,PGM(3)* 2 = 0.375,并且未观察到与Hardy-Weinberg平衡的偏差。该信息在遗传学和法医学中的应用表明,多态性信息含量为0.5163,杂合度为0.4872,判别力为0.5986,父子排除概率为0.1794。 DNA水平的基因座多态性分析也将为疾病易感性和连锁分析提供重要数据。

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