{"symbol":"FARS2","synonyms":["SPG77","FARS1","HSPC320","COXPD14","DJ520B18.2"],"name":"phenylalanyl-tRNA synthetase 2, mitochondrial","description":"This gene encodes a protein that transfers phenylalanine to its cognate tRNA. This protein localizes to the mitochondrion and plays a role in mitochondrial protein translation. Mutations in this gene can cause combined oxidative phosphorylation deficiency 14 (Alpers encephalopathy). Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]","ncbiEntrezGeneId":10667,"ncbiEntrezGeneUrl":"http://www.ncbi.nlm.nih.gov/gene/10667","proteins":[{"symbol":"SYFM_HUMAN","href":"/api/1.0/protein/SYFM_HUMAN"}],"hgncRootFamilies":[{"name":"Aminoacyl tRNA synthetases","href":"/api/1.0/gene_family/Aminoacyl+tRNA+synthetases"}]}