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A study of a single variant allele (rs1426654) of the pigmentation‐related gene SLC24A5 in Greek subjects

Gerasimos Dimisianos

Department of Medical Genetics, University of Athens, Agia Sophia Children’s Hospital, Athens, Greece

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Irene Stefanaki

Department of Dermatology, University of Athens, Andreas Sygros Hospital, Athens, Greece

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Vicky Nicolaou

Department of Dermatology, University of Athens, Andreas Sygros Hospital, Athens, Greece

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Vana Sypsa

Department of Hygiene and Epidemiology, University of Athens, Athens, Greece

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Christina Antoniou

Department of Dermatology, University of Athens, Andreas Sygros Hospital, Athens, Greece

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Myrto Poulou

Department of Medical Genetics, University of Athens, Agia Sophia Children’s Hospital, Athens, Greece

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Othon Papadopoulos

Department of Dermatology, University of Athens, Andreas Sygros Hospital, Athens, Greece

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Helen Gogas

Oncology Unit, Department of Medicine, University of Athens, Laikon Hospital, Athens, Greece

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Emmanouel Kanavakis

Department of Medical Genetics, University of Athens, Agia Sophia Children’s Hospital, Athens, Greece

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Electra Nicolaidou

Department of Dermatology, University of Athens, Andreas Sygros Hospital, Athens, Greece

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Andreas D. Katsambas

Department of Dermatology, University of Athens, Andreas Sygros Hospital, Athens, Greece

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Alexander J. Stratigos

Department of Dermatology, University of Athens, Andreas Sygros Hospital, Athens, Greece

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First published: 12 January 2009
Cited by: 6
Alexander J. Stratigos, MD, Department of Dermatology, University of Athens, Andreas Sygros Hospital, Athens, Greece, Tel.: (+30)2107258476, Fax: (+30)2107239965, e‐mail: alstrat@hol.gr

Abstract

Abstract: The SLC24A5 gene, the human orthologue of the zebrafish golden gene, has been shown to play a key role in human pigmentation. In this study, we investigate the prevalence of the variant allele rs1426654 in a selected sample of Greek subjects. Allele‐specific polymerase chain reaction was performed in peripheral blood samples from 158 attendants of a dermatology outpatient service. The results were correlated with pigmentary traits and MC1R genotype. The vast majority of subjects (99%) were homozygous for the Thr111 allele. Only two subjects from the control group (1.26%) were heterozygous for the alanine and threonine allele. Both of these Thr111/Ala111 heterozygotes carried a single polymorphism of MC1R (one with the V92M variant and another with the V60L variant). Following reports of the rs1426654 polymorphism reaching fixation in the European population, our study of Greek subjects showed a prevalence of the Thr111 allele, even among subjects with darker skin pigmentation or phototype.

Number of times cited: 6

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