Identification of a novel variant of COL4A5 gene in a pedigree affected with Alport syndrome.
10.3760/cma.j.issn.1003-9406.2020.08.001
- Author:
Xiaowei LIU
1
;
Ming GAO
;
Yang ZOU
;
Lijuan WANG
;
Ranran KANG
;
Peiwen XU
;
Yuping NIU
;
Sexin HUANG
;
Jie LI
;
Hongqiang XIE
;
Yuan GAO
Author Information
1. Center for Reproductive Medicine, National Research Center for Assisted Reproductive Technology and Reproductive Genetics, Key Laboratory for Reproductive Endocrinology of the Ministry of Education, Shandong University, Jinan, Shandong 250001, China. gaoyuan@sduivf.com.
- Publication Type:Journal Article
- From:
Chinese Journal of Medical Genetics
2020;37(8):807-810
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVE:To explore the genetic basis for a pedigree affected with Alport syndrome.
METHODS:Next generation sequencing and Sanger sequencing was carried out to detect potential variant of the COL4A5 gene among members from the pedigree and 100 unrelated healthy controls.
RESULTS:A novel missense c.3293G>T (p.Gly1098Val) variant was found in the COL4A5 gene among 6 affected members but not the unaffected members of the pedigree or the 100 healthy controls. According to the American College of Medical Genetics and Genomics standards and guidelines, the c.3293G>T variant was classified as pathogenic (PP1-strong+PM1+PM2+PP3+PP4).
CONCLUSION:By destructing the Gly-X-Y structure of its protein product, the c.3293G>T variant of the COL4A5 gene probably underlies the Alport syndrome in this pedigree. Above finding has enriched the spectrum of COL4A5 variants.
