Analysis of C2ORF71 gene variant in a Chinese patient with retinitis pigmentosa.
10.3760/cma.j.cn511374-20201223-00902
- VernacularTitle:一例视网膜色素变性患者
C2ORF71基因的变异分析
- Author:
Man LIU
1
;
Yilu LU
;
Yongxin MA
Author Information
1. Department of Medical Genetics, West China Hospital, Sichuan University, Chengdu, Sichuan 610041, China. mayongxin@gmail.com.
- Publication Type:Journal Article
- MeSH:
Asians/genetics*;
China;
Humans;
Mutation;
Pedigree;
Retinitis Pigmentosa/genetics*;
Whole Exome Sequencing
- From:
Chinese Journal of Medical Genetics
2022;39(1):52-55
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVE:To explore the genetic basis for a Chinese patient with retinitis pigmentosa (RP).
METHODS:Whole exome sequencing (WES) was carried out to screen potential variant in the proband. Candidate variants were determined by taking consideration of clinical phenotype. Sanger sequencing was used to verify the variant in the proband and his parents.
RESULTS:The proband was found to harbor compound heterozygous variants of c.8G>A (p.Cys3Tyr) and c.958_959insA (p.Arg320Glnfs*29) in the C2ORF71 gene, which has derived from his father and mother, respectively. Both variants were unreported previously. Based on the ACMG guidelines, they were predicted to be likely pathogenic and pathogenic, respectively.
CONCLUSION:The novel compound heterozygous variants of the C2ORF71 gene probably underlay the pathogenesis of RP in the proband. Above finding has enriched the spectrum of C2ORF71 gene mutations and facilitated genetic counseling for the family.
