Yuasa I, Suenaga K, Umetsu K, Ito K, Robinet-Levy M
Department of Legal Medicine, Tottori University School of Medicine, Yonago, Japan.
Hum Genet. 1987 Nov;77(3):255-8. doi: 10.1007/BF00284480.
It has been demonstrated that the genetic polymorphism of human serum orosomucoid (ORM) is controlled by polymorphic ORM1 and monomorphic ORM2 loci. In this study a Japanese family was encountered in which several members had puzzling electrophoretic patterns consisting of four bands. The ORM patterns were due to the products of a duplicated ORM1 locus haplotype (ORM1 2.1) or the products of new variant alleles at the ORM2 locus. The ORM1 2.1 haplotype is very common in the Japanese population, occurring at an allele frequency of 0.16. The increased occurrence of ORM12-1 and the heterogeneity in band intensity among ORM12-1 phenotypes could be explained in terms of a duplicated gene ORM1 2.1. The ORM2 locus proved to be polymorphic, with six alleles in the Japanese population.
已经证明,人血清类粘蛋白(ORM)的遗传多态性由多态性ORM1和单态性ORM2位点控制。在本研究中,遇到一个日本家庭,其中几个成员具有由四条带组成的令人困惑的电泳图谱。ORM模式是由于重复的ORM1位点单倍型(ORM1 2.1)的产物或ORM2位点新变异等位基因的产物。ORM1 2.1单倍型在日本人群中非常常见,等位基因频率为0.16。ORM12 - 1的发生率增加以及ORM12 - 1表型之间条带强度的异质性可以用重复基因ORM1 2.1来解释。事实证明,ORM2位点具有多态性,在日本人群中有六个等位基因。