Variant analysis of SEC23B gene in 4 families with congenital dyserythropoietic anemia.
10.3760/cma.j.cn511374-20200327-00211
- VernacularTitle:四个先天性红细胞生成异常性贫血家系的
SEC23B基因变异分析
- Author:
Yin FENG
1
;
Panlai SHI
;
Ning LIU
;
Xiangdong KONG
Author Information
1. Center of Genetic and Prenatal Diagnosis, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan 450002, China. kongxd@263.net.
- Publication Type:Journal Article
- MeSH:
Anemia, Dyserythropoietic, Congenital/genetics*;
Exons/genetics*;
High-Throughput Nucleotide Sequencing;
Humans;
Mutation;
Vesicular Transport Proteins/genetics*
- From:
Chinese Journal of Medical Genetics
2021;38(8):727-730
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVE:To identify the pathogenic variants of 4 patients with hemolytic anemia of unknown cause.
METHODS:Peripheral blood samples of the patients and their family members were collected to extract DNA. The coding region and splice region in all exons of gene of erythrocyte related diseases were analyzed by using target sequence capture and high-throughput sequencing technology. Suspected pathogenic variants were verified by PCR combined Sanger sequencing technology.
RESULTS:Each of the probands was detected two compound heterozygous variants, and CDA II was diagnosed. Six variants were detected in the 4 probands, four variants were reported and the other two were first reported.
CONCLUSION:By high-throughput sequencing, gene variant of CDA II be analyzed fast and accurately. It is an effective supplement to convenional diagnostic methods. Furthermore, the novel variant sites have enriched the variant database of the SEC23B gene.
