Identification of two novel variants, c.-35A>T and c.[-35A>T, 725T>G], in the FUT1 gene in a patient exhibiting the para-Bombay phenotype.

Background: Reduced or absent H antigens on red cells with the (para-)Bombay phenotype can arise from FUT1 gene mutations, impacting the structure and function of 1,2-L-fucosyltransferase 1 (1,2-L-FucT1). Here, we identified the novel mutations in one patient displaying the para-Bombay phenotype and examined the potential molecular mechanisms underlying this phenotype.

Materials And Methods: ABH antigens and antibodies were detected in patient's blood and saliva using serological methods.

Characterization of GYP(B-A-B) hybrid glycophorins among Thai blood donors with Mi-positive phenotypes.

Background: GYPA and GYPB genes encode the antigens of the MNS blood group system carried on glycophorin A (GPA) and glycophorin B (GPB), or on a hybrid molecule of GPA and GPB. GP hybrid variants are created through unequal crossing over and gene conversion, typically from the parent genes GYPA and GYPB. In the present study, we characterized the GYP(B-A-B) hybrid variants among Thai blood donors with Mi-positive phenotypes using PCR-based coupled to DNA sequencing techniques.

Identification of Lutheran Blood Groups and Genetic Variants within among Thai Blood Donors.

Background: Lu and Lu are inherited as codominant allelic characters resulting from a single nucleotide variant (SNV) of the basal cell adhesion molecule () gene. Red cells of the dominantly inherited suppressor of the Lutheran antigens In(Lu) phenotypically appear as Lu(a-b-) by the haemagglutination test. In(Lu) resulted from heterozygosity for mutations within the erythroid-specific Krüppel-like factor 1 () gene.