Literature DB >> 24772942

Identification of a GJA3 mutation in a Chinese family with congenital nuclear cataract using exome sequencing.

Yi Guo, Lamei Yuan, Junhui Yi, Jingjing Xiao, Hongbo Xu, Hongwei Lv, Wei Xiong, Wen Zheng, Liping Guan, Jianguo Zhang, Hong Xiang, Yong Qi, Hao Deng.   

Abstract

Congenital cataract, a clinically and genetically heterogeneous lens disorder is defined as any opacity of the lens presented from birth and is responsible for approximately 10% of worldwide childhood poor vision or blindness. To identify the genetic defect responsible for congenital nuclear cataract in a four-generation Chinese Han family, exome and direct Sanger sequencings were conducted and a missense variant c.139G>A (p.D47N) in the gap junction protein-alpha 3 gene (GJA3) was identified. The variant co-segregated with patients of the family and was not observed in unaffected family members or normal controls. The above findings indicated that the variant was a pathogenic mutation. The mutation p.D47N was found in the first extracellular loop (El) domain of GJA3 protein. Our data suggest that exome sequencing is a powerful tool to discover mutation(s) in cataract, a disorder with high genetic heterogeneity. Our findings may also provide new insights into the cause and diagnosis of congenital nuclear cataract and have implications for genetic counseling.

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Year:  2013        PMID: 24772942

Source DB:  PubMed          Journal:  Indian J Biochem Biophys        ISSN: 0301-1208            Impact factor:   1.918


  7 in total

Review 1.  Inherited Congenital Cataract: A Guide to Suspect the Genetic Etiology in the Cataract Genesis.

Authors:  Olga Messina-Baas; Sergio A Cuevas-Covarrubias
Journal:  Mol Syndromol       Date:  2017-02-07

2.  Use of high-throughput targeted exome sequencing in genetic diagnosis of Chinese family with congenital cataract.

Authors:  Ming-Fu Ma; Lian-Bing Li; Yun-Qi Pei; Zhi Cheng
Journal:  Int J Ophthalmol       Date:  2016-05-18       Impact factor: 1.779

3.  A novel COL4A5 mutation identified in a Chinese Han family using exome sequencing.

Authors:  Xiaofei Xiu; Jinzhong Yuan; Xiong Deng; Jingjing Xiao; Hongbo Xu; Zhaoyang Zeng; Liping Guan; Fengping Xu; Sheng Deng
Journal:  Biomed Res Int       Date:  2014-07-06       Impact factor: 3.411

4.  Identification of novel pathogenic ABCA4 variants in a Han Chinese family with Stargardt disease.

Authors:  Qin Xiang; Yanna Cao; Hongbo Xu; Yi Guo; Zhijian Yang; Lu Xu; Lamei Yuan; Hao Deng
Journal:  Biosci Rep       Date:  2019-01-15       Impact factor: 3.840

5.  Identification of a novel EVC variant in a Han-Chinese family with Ellis-van Creveld syndrome.

Authors:  Xiangjun Huang; Yi Guo; Hongbo Xu; Zhijian Yang; Xiong Deng; Hao Deng; Lamei Yuan
Journal:  Mol Genet Genomic Med       Date:  2019-07-23       Impact factor: 2.183

6.  Identification of a Novel Missense FBN2 Mutation in a Chinese Family with Congenital Contractural Arachnodactyly Using Exome Sequencing.

Authors:  Hao Deng; Qian Lu; Hongbo Xu; Xiong Deng; Lamei Yuan; Zhijian Yang; Yi Guo; Qiongfen Lin; Jingjing Xiao; Liping Guan; Zhi Song
Journal:  PLoS One       Date:  2016-05-19       Impact factor: 3.240

7.  Novel 6-bp deletion in MEF2A linked to premature coronary artery disease in a large Chinese family.

Authors:  Dong-Ling Xu; Hong-Liang Tian; Wei-Li Cai; Jie Zheng; Min Gao; Ming-Xiang Zhang; Zhao-Tong Zheng; Qing-Hua Lu
Journal:  Mol Med Rep       Date:  2016-05-18       Impact factor: 2.952

  7 in total

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