Analysis of ANK1 gene mutation in a family with hereditary spherocytosis type Ⅰ.
10.3760/cma.j.issn.1003-9406.2019.10.012
- Author:
Dongliang LI
1
;
Bolun LI
;
Suxin LI
;
Wenjing LI
;
Youjun WANG
;
Xiao GUO
Author Information
1. Bethune International Peace Hospital of PLA, Shijiazhuang, Hebei 050082, China. ldle2008@sina.com.
- Publication Type:Journal Article
- MeSH:
Ankyrins;
genetics;
High-Throughput Nucleotide Sequencing;
Humans;
Male;
Mutation;
Open Reading Frames;
Spherocytosis, Hereditary;
genetics
- From:
Chinese Journal of Medical Genetics
2019;36(10):999-1001
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVE:To detect the disease-causing mutation in a family with hereditary spherocytosis type Ⅰ.
METHODS:Genomic DNA was extracted from peripheral blood samples of the proband and his relatives. Next-generation sequencing was used to detect the mutations of relevant genes. Suspected pathogenic mutation was verified by Sanger sequencing.
RESULTS:The proband was found to harbor a novel frameshifting mutation in the coding region of ANK1 gene, which has resulted in abnormal structure or function of the protein. The mutation was confirmed by Sanger sequencing, with both his father and brother found to have carried the same mutation.
CONCLUSION:The c.247delG mutation of proband hereditary spherocytosis typeⅠin this family due to mutation of the ANK1 gene．.
