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Distribution of OCA2∗481Thr and OCA2∗615Arg, associated with hypopigmentation, in several additional populations

Authors :
Isao Yuasa
Yasuo Fukumori
Junko Fujihara
Feng Jin
Kazuo Umetsu
Haruo Takeshita
Hiroaki Nishimukai
Shinji Harihara
Naruya Saitou
Source :
Legal Medicine. 13:215-217
Publication Year :
2011
Publisher :
Elsevier BV, 2011.

Abstract

Two mutants, OCA2*481Thr (c.1441G > A, p.Ala481Thr) and OCA2*615Arg (c.1844A > G, p.His615Arg), in the OCA2 (oculocutaneous albinism type II) gene are associated with hypopigmentation in East Asians. Here, these two alleles were studied to assess the frequencies in five different populations. In addition, the allele frequency of OCA2*615Arg was investigated in seven populations. Among a total of 24 global populations investigated, Oroqens in Heihe showed the highest frequency for OCA2*481Thr (0.519), and among 26 populations, Han Chinese in Changsha showed the highest frequency for OCA2*615Arg (0.673). This study confirmed that these two East Asian-specific alleles are characteristic of northern and central-southern East Asian populations. (C) 2011 Elsevier Ireland Ltd. All rights reserved.

Details

ISSN :
13446223
Volume :
13
Database :
OpenAIRE
Journal :
Legal Medicine
Accession number :
edsair.doi.dedup.....27ac2462d98869b3f3b3514162cef36c