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COL4A3 mutations cause focal segmental glomerulosclerosis Free
Jingyuan Xie1,†, Xiaoxi Wu2,†, Hong Ren1, Weiming Wang1, Zhaohui Wang1, Xiaoxia Pan1, Xu Hao1, Jun Tong1, Jun Ma1, Zhibin Ye3, Guoyu Meng4, Yufei Zhu2, Krzysztof Kiryluk5, Xiangyin Kong2, Landian Hu2,*, and Nan Chen1,*
1 Department of Nephrology, Shanghai Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China
2 State Key Laboratory for Medical Genomics, Institute of Health Sciences, Shanghai Jiao Tong University School of Medicine (SJTUSM) and Shanghai Institutes for Biological Sciences (SIBS), Chinese Academy of Sciences (CAS), Shanghai, China
3 Nephrology Department, Huadong Hospital Affiliated to Fudan University, Shanghai, China
4 State Key Laboratory for Medical Genomics, Shanghai Institute of Hematology, Rui Jin Hospital Affiliated to Shanghai Jiao Tong University School of Medicine, Shanghai, China
5 Division of Nephrology, Department of Medicine, College of Physicians and Surgeons, Columbia University, New York, USA *Correspondence to:Nan Chen, E-mail: cnrj100@126.com; Landian Hu, E-mail: ldhu@sibs.ac.cn
J Mol Cell Biol, Volume 7, Issue 2, April 2015, 184-184,  https://doi.org/10.1093/jmcb/mjv023

In this article, there were two annotation mistakes about the precise deletion position in COL4A3 and COL4A4 mutations in ARAS patients (summarized in Figure 2E). This was caused by a bug in the old version (v3.4) of Variant Caller for Ion Torrent. The variant in family AP5 should be described as ‘chr2:227942771delG’, instead of ‘chr:227942770delG’, in the COL4A4 gene. The variant identified in family AP1 should be described as ‘chr2:228172490delA’, instead of ‘chr:228172489delA’, in the COL4A3 gene.


Volume 7, Issue 2
April 2015