{"count":3,"next":null,"previous":null,"results":[{"gene_data":{"alias":["FLJ12528"],"biotype":"protein_coding","hgnc_id":"HGNC:30740","gene_name":"threonyl-tRNA synthetase 2, mitochondrial (putative)","omim_gene":["612805"],"alias_name":["threonine tRNA ligase 2, mitochondrial"],"gene_symbol":"TARS2","hgnc_symbol":"TARS2","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"1:150459887-150480078","ensembl_id":"ENSG00000143374"}},"GRch38":{"90":{"location":"1:150487364-150507609","ensembl_id":"ENSG00000143374"}}},"hgnc_date_symbol_changed":"2007-02-23"},"entity_type":"gene","entity_name":"TARS2","confidence_level":"2","penetrance":null,"mode_of_pathogenicity":"","publications":["PMID: 24827421 - Compound heterozygous variants in TARS2 were reported in the proband and his affected sister - a missense mutation (c.845C>T,  p.Pro282Leu) and a nucleotide change in position +3 of intron 6 (g.4255A>G, c.695+3A>G). 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