Abstract
The amelogenin (AMEL) is widely used in many multiplex PCR kits for gender determination. However, the null of amelogenin Y (AMELY) can result in the incorrect genotyping of male samples as females. In this study, we report the deletion of AMELY in two cases with a deletion frequency of 0.019% (2/10526) in our laboratory. The deletion region with AMELY was mapped by using other twelve loci, which shows the class I deletion pattern. Further, the Y chromosome short tandem repeat (Y-STR) typing shows that these two cases share the same haplotype with other two cases from previous reports. The haplogroup of the two cases was predicted as O3 haplogroup with a 100% probability. Altogether, this study will provide evidence to further demonstrate the deletion of AMELY in Chinese population.
Original language | English (US) |
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Pages (from-to) | 290-292 |
Number of pages | 3 |
Journal | Legal Medicine |
Volume | 16 |
Issue number | 5 |
DOIs | |
State | Published - 2014 |
Externally published | Yes |
Keywords
- AMEL
- Chinese population
- Deletion
- DYS458
- Haplogroup
ASJC Scopus subject areas
- Pathology and Forensic Medicine
- Issues, ethics and legal aspects
- Medicine(all)