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• W3025611196 abstract "Background The low‐incidence antigen St a of the MNS system is usually associated with the GP(B‐A) hybrid molecule, which carries the ‘N’ antigen at the N terminus. The GP(A‐A) molecule with trypsin‐resistant M antigen has been found in a few St(a+) individuals. Materials and Methods Among Japanese blood donors, we screened 24 292 individuals for the presence of St(a+) with trypsin‐resistant ‘N’ antigen and 193 009 individuals for the presence of St(a+) with trypsin‐resistant M antigen. The breakpoints responsible for the St a antigen were analysed by sequencing the genomic DNAs. Results A total of 1001 (4·1%) individuals were identified as St(a+) with trypsin‐resistant ‘N’ antigen. Out of 1001 individuals, 115 were selected randomly for sequencing. Two novel GYP*Sch ( GYP*401 ) variants with new intron 3 breakpoints of GYPA were detected in three cases. Twenty‐five (0·013%) individuals were identified as St(a+) with trypsin‐resistant M antigen. Five individuals had the GYP(A‐ψB‐A) hybrid allele; two of these five individuals were GYP*Zan ( GYP*101.01 ), and the remaining three had a novel GYP(A‐ψB‐A) allele with the first breakpoint in GYPA exon A3 between c.178 and c.203. Nine individuals had a novel GYP(A‐E‐A) allele with GYPE exon E2 and pseudoexon E3 instead of GYPA exon A2 and A3. The 11 remaining individuals had a novel GYP(A‐A) allele with a 9‐bp deletion that included the donor splice site of intron 3 of GYPA . Conclusion Our finding on diversity of glycophorin genes responsible for St a antigen provides evidence for further complexity in the MNS system." @default.
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• W3025611196 date "2020-05-11" @default.
• W3025611196 modified "2023-09-26" @default.
• W3025611196 title "Novel hybrid genes and a splice site mutation encoding the St^aantigen among Japanese blood donors" @default.
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• W3025611196 doi "https://doi.org/10.1111/vox.12921" @default.
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