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Distribution of OCA2∗481Thr and OCA2∗615Arg, associated with hypopigmentation, in several additional populations
- 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.
- Subjects :
- Veterinary medicine
Han chinese
Asia
Genotype
genetic structures
Biology
Polymorphism, Single Nucleotide
Pathology and Forensic Medicine
Asian People
Gene Frequency
Population specific
Ethnicity
medicine
Humans
Allele
Allele frequency
Hypopigmentation
Genetics
OCA2
Membrane Transport Proteins
medicine.disease
Oculocutaneous albinism
Issues, ethics and legal aspects
Genetics, Population
Albinism, Oculocutaneous
Population study
medicine.symptom
Subjects
Details
- ISSN :
- 13446223
- Volume :
- 13
- Database :
- OpenAIRE
- Journal :
- Legal Medicine
- Accession number :
- edsair.doi.dedup.....27ac2462d98869b3f3b3514162cef36c