Literature DB >> 12445310

A nonsense mutation in exon 3 results in the HLA-B null allele B*5127N.

J Y Hou1, E Luning Prak, J Kearns, J Wu, S Bassinger, S Birkos, T M Williams, M Kamoun.   

Abstract

A new HLA-B null allele has been identified within the B*51 group by combined serological and molecular typing of an Italian Caucasoid family. Serological data indicated that the proband typed homozygous for A2 and B60. Confirmatory typing using sequence specific oligonucleotide hybridization (SSPOH) detected a second B allele within the B*51 group. Allele specific typing (SSP) for B*51 subtypes, including the known B*5111N allele, was performed, and typing results were consistent with B*5101, suggesting the presence of a new null variant. Cloning and sequencing of this allele identified a B*5101 variant with a nonsense mutation in exon 3. This new null allele has been designated B*5127N. The combined use of serologic and DNA-based typing methods facilitates the identification of null and low-expression alleles. An overview of null alleles of class I HLA is presented.

Entities:  

Mesh:

Substances:

Year:  2002        PMID: 12445310     DOI: 10.1034/j.1399-0039.2002.600309.x

Source DB:  PubMed          Journal:  Tissue Antigens        ISSN: 0001-2815


  1 in total

1.  Cataloging coding sequence variations in human genome databases.

Authors:  Hong-Hee Won; Hee-Jin Kim; Kyung-A Lee; Jong-Won Kim
Journal:  PLoS One       Date:  2008-10-30       Impact factor: 3.240

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.