Abstract
The ABO system is the most important of all blood group systems in transfusion practice. The subgroup gives a weak reaction when treated with anti-A or anti-B. The most common subgroup found in Thai blood donors is subgroup A3, which is characterized by mixed-field agglutination when reacted with anti-A and anti-A,B, was caused by mutation in the ABO gene, especially in the exon 7. In the present study mutation in A3 were charactered in exon 7 of the ABO gene in 10 A3 phenotype Thai blood donors from the National Blood Centre, Thai Red Cross Society by PCR amplification and DNA sequencing. Mutations in exon 7 were identified in the A allele of six cases. In four cases, mutations were detected at positions 646T>A, 681G>A, 771C>T and 829G>A. One case showed a double mutations at positions 467C>T and 745C>T and one case showed a mutation at position 467C>T. Four cases showed wild type exon 7 as A101 allele. These mutations were previously reported in BGMUT database and no novel mutation was identified. These data suggest genetic heterogeneity in A3 phenotype in Thai blood donors.
| Original language | English |
|---|---|
| Pages (from-to) | 379-385 |
| Number of pages | 7 |
| Journal | Journal of the Medical Association of Thailand |
| Volume | 94 |
| Issue number | 3 |
| Publication status | Published - Mar 2011 |
Keywords
- A phenotype
- ABO gene
- Blood group
- Genetic mutation
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