假基因
打字
遗传学
人类白细胞抗原
生物
等位基因
外显子
序列(生物学)
底漆(化妆品)
内含子
分子生物学
基因
抗原
化学
基因组
有机化学
作者
Sanghwan Ko,Heung‐Bum Oh,Yong–Hak Sohn,J. H. Jun,O.‐J. Kwon
标识
DOI:10.1111/j.1399-0039.2010.01605.x
摘要
We encountered a case that exhibited a discrepancy in human leukocyte antigen-A (HLA-A) type determined by sequence-based typing (SBT) and sequence-specific primer (SSP) molecular typing. The child of this case was identified as A* 02:01 homozygote and A* 02, A* 24, respectively. The HLA-A type of his father was A* 02:01, 26:01, but low-resolution SSP also showed unexpected amplification with A* 24 primers as with the child. Serologic typing of the child and the father was A2/blank and A2/A26, respectively. Sequencing analysis of the A* 24 variant in the child and the father showed a complete deletion of all introns of the A* 24:02 allele. Though rare, this type of processed pseudogene variant can be one of the causes of discrepancies between high- and low-resolution HLA typing.
科研通智能强力驱动
Strongly Powered by AbleSci AI