rs2139666763
This variant is located in the CARS2 gene.
▶ClinVar annotation
Combined oxidative phosphorylation defect type 27
View on ClinVar →About CARS2
This gene encodes a putative member of the class I family of aminoacyl-tRNA synthetases. These enzymes play a critical role in protein biosynthesis by charging tRNAs with their cognate amino acids. This protein is encoded by the nuclear genome but is likely to be imported to the mitochondrion where it is thought to catalyze the ligation of cysteine to tRNA molecules. A splice-site mutation in this gene has been associated with a novel progressive myoclonic epilepsy disease with similar symptoms to MERRF syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jun 2017]
View all CARS2 variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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