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Identification of a novel FUT1 allele of para-Bombay phenotype / 中华医学遗传学杂志
Chinese Journal of Medical Genetics ; (6): 636-638, 2019.
Artículo en Chino | WPRIM | ID: wpr-771949
ABSTRACT
OBJECTIVE@#To explore the molecular basis for an individual with para-Bombay phenotype of the H blood group.@*METHODS@#Intron 5 to 3'-UTR of the ABO gene and exon 4 of the FUT1 gene were amplified with PCR and subjected to direct sequencing. Mutations of the FUT1 gene were identified by TOPO cloning sequencing.@*RESULTS@#Direct sequencing showed that her ABO genotype was B101/O01. TOPO cloning sequencing found that this individual had three mutations of the FUT1 gene, including an heterozygous AG deletion (CAGAGAG→CAGAG) at position 547 to 552, and two C→T mutations at positions 35 (C35T) and 293 (C293T) on the other homologous chromosome. The two alleles comprised a new recombination of mutations c.35T>C and c.293C>T, and the sequence has been submitted to NCBI (No. MG597611).@*CONCLUSION@#A novel combination of FUT1 alleles with c.35 C>T and c.293C>T has been identified in an individual with para-Bombay phenotype.
Asunto(s)
Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: Fenotipo / Sistema del Grupo Sanguíneo ABO / Alelos / Fucosiltransferasas / Genética / Genotipo Tipo de estudio: Estudio diagnóstico / Estudio pronóstico Límite: Femenino / Humanos Idioma: Chino Revista: Chinese Journal of Medical Genetics Año: 2019 Tipo del documento: Artículo

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Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: Fenotipo / Sistema del Grupo Sanguíneo ABO / Alelos / Fucosiltransferasas / Genética / Genotipo Tipo de estudio: Estudio diagnóstico / Estudio pronóstico Límite: Femenino / Humanos Idioma: Chino Revista: Chinese Journal of Medical Genetics Año: 2019 Tipo del documento: Artículo