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Histo-Blood Group A Variants, O Variants, and Their Alleles

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Handbook of Glycosyltransferases and Related Genes

Abstract

The allelic basis of the blood group ABO system was established in 1990 when the genes for human blood group A and B synthesizing glycosyltransferases were cloned (Yamamoto et al. 1990) and it was shown that there were only four amino acid differences between the blood group A and B synthesizing glycosyltransferases GTA and GTB (Arg/Gly176, Gly/Ser235, Leu/Met266 and Gly/Ala268). The O gene had a single-nucleotide deletion which resulted in a truncated inactive enzyme. Since the ABO system is based on red blood cell agglutination, it has been possible to identify many other alleles from routine blood typing carried out worldwide in blood banking centers (Storry and Olsson 2009; Yamamoto et al. 2012). Thus subgroups of A and B can be identified by weak and/or anomalous agglutination patterns in forward and reverse blood typing. DNA sequencing is carried out on any samples suspected of having alleles other than the original three. Currently (May 2013) 306 ABO alleles are tabulated in the blood group antigen mutation database (BGMUT) that is part of the dbRBC resource of the National Center for Biotechnology (Patnaik et al. 2012). However, new alleles are continually being identified. ABO is therefore considered to be one of the most genetically complex blood group systems.

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Correspondence to Sen-itiroh Hakomori .

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Hakomori, Si., Palcic, M. (2014). Histo-Blood Group A Variants, O Variants, and Their Alleles. In: Taniguchi, N., Honke, K., Fukuda, M., Narimatsu, H., Yamaguchi, Y., Angata, T. (eds) Handbook of Glycosyltransferases and Related Genes. Springer, Tokyo. https://doi.org/10.1007/978-4-431-54240-7_159

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