等位基因
单倍型
遗传学
载脂蛋白E
GenBank公司
生物
等位基因频率
单核苷酸多态性
基因
基因型
疾病
医学
病理
作者
Davide Seripa,Maria G. Matera,Antonio Daniele,Alessandra Bizzarro,Monica Rinaldi,Carolina Gravina,Luigi Bisceglia,Rosa Maria Corbo,Francesco Panza,Vincenzo Solfrizzi,Vito Michele Fazio,Gloria Dal Forno,Carlo Masullo,Bruno Dallapiccola,Alberto Pilotto
标识
DOI:10.1111/j.1469-1809.2006.00344.x
摘要
Summary The human apoE gene ( APOE , GenBank accession AF261279) shows a common polymorphism, with the three ɛ2, ɛ3 and ɛ4 alleles resulting from the haplotypes of two C→T SNPs. However, whereas the three common T‐T, T‐C and C‐C haplotypes corresponding to the ɛ2, ɛ3 and ɛ4 alleles are well known, the last C‐T haplotype (GenBank accession AY077451), encoding a fourth apoE allele, has rarely been reported. We detected this fourth allele in a Caucasian patient with motor neuron disease (MND). According to the literature we refer to this allele as ɛ3r. Although several explanations may be proposed for its formation, the existence of this fourth allele is consistent with the evolutionary hypothesis generally accepted for the apoE alleles. The rarity and physiological role of ɛ3r remains to be explained, and requires further investigation.
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