桑格测序
遗传学
生物
基因
候选基因
外显子
DNA测序
遗传变异
计算生物学
基因检测
基因组学
外显子组测序
2型糖尿病
突变
基因组
糖尿病
内分泌学
作者
Yue Luo,Jiahui Jin,Liyi Li,Huiping Wu,Xiaoou Shan
出处
期刊:Chinese journal of medical genetics
日期:2021-09-10
卷期号:38 (9): 891-894
被引量:1
标识
DOI:10.3760/cma.j.cn511374-20200626-00476
摘要
Objective To explore the genetic basis for a juvenile with maturity-onset diabetes of the young type 12(MODY12). Methods High-throughput sequencing was carried out to screen for the variants. Candidate variant was verified by Sanger sequencing. Pathogenity of the variant was predicted by searching the genetic databases and analysis by using bioinformatic software. Results Genetic testing indicated that the patient and his mother have both carried a heterozygous c.3976G>A variant (p.Glu1326Lys) in exon 32 of the ABCC8 gene. Prediction of the protein structure suggested the variant to be deleterious. Based on the guidelines of the American College of Medical Genetics and Genomics, the variant was predicted to be uncertain significance. Conclusion Whether the c.3976G>A variant of the ABCC8 gene is the cause of the disease in this patient or not depends on the functional studies and more case data. Above finding has enriched the spectrum of ABCC8 gene variants.
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