Literature DB >> 11045762

Novel mutations, including a novel G659A missense mutation, of the FUT1 gene are responsible for the para-Bombay phenotype.

C F Sun1, M D Lo, C H Lee, D C Chu.   

Abstract

Para-Bombay phenotype, with an estimated incidence of 1 in 8000 in Taiwanese residents based on serological analysis, is caused by aberrant alpha(1,2)-fucosyltransferase function and hence diminished H-antigen synthesis. In an individual with para-Bombay phenotype, DNA sequencing revealed two missense mutations previously reported C658T mutation and a novel G659A mutation. Haplotype analysis with restriction enzyme digestion showed that the two mutations are located on opposing alleles of the H (FUT1) gene and lead to compound heterozygosity. Since no other known genetic changes were evident, it appears that the new missense mutation, G659A, is deleterious to the alpha(1,2)-fucosyltransferase function encoded by the H (FUT1) gene.

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Year:  2000        PMID: 11045762

Source DB:  PubMed          Journal:  Ann Clin Lab Sci        ISSN: 0091-7370            Impact factor:   1.256


  2 in total

1.  Two Novel α 1,2-Fucosyltransferase Alleles in an H-Deficient Phenotype Individual.

Authors:  Ziyi He; Fuping Liu
Journal:  Transfus Med Hemother       Date:  2014-08-17       Impact factor: 3.747

2.  A Very Rare Case with Particular H-deficient Phenotypes.

Authors:  Min Song; Shuming Zhao; Tianlun Jiang; Hua Lu
Journal:  Indian J Hematol Blood Transfus       Date:  2018-01-11       Impact factor: 0.900

  2 in total

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