(Tyrosyl-tRNA Synthetase 2, Mitochondrial (YARS2))
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Latest Publications for our YARS2 products: "Phenotypic variability and identification of novel YARS2 mutations in YARS2 mitochondrial myopathy, lactic acidosis and sideroblastic anaemia." in: Orphanet journal of rare diseases, Vol. 8, pp. 193, (2014) (PubMed).
: "Mutation of the mitochondrial tyrosyl-tRNA synthetase gene, YARS2, causes myopathy, lactic acidosis, and sideroblastic anemia--MLASA syndrome." in: American journal of human genetics, Vol. 87, Issue 1, pp. 52-9, (2010) (PubMed).
: "Crystal structure of human mitochondrial tyrosyl-tRNA synthetase reveals common and idiosyncratic features." in: Structure (London, England : 1993), Vol. 15, Issue 11, pp. 1505-16, (2007) (PubMed).
: "Toward the full set of human mitochondrial aminoacyl-tRNA synthetases: characterization of AspRS and TyrRS." in: Biochemistry, Vol. 44, Issue 12, pp. 4805-16, (2005) (PubMed).
: "Human mitochondrial TyrRS disobeys the tyrosine identity rules." in: RNA (New York, N.Y.), Vol. 11, Issue 5, pp. 558-62, (2005) (PubMed).
Synonyms and alternative names related to YARS2tyrosyl-tRNA synthetase 2 (mitochondrial) (Yars2), tyrosyl-tRNA synthetase 2 (Yars2), tyrosyl-tRNA synthetase 2 (YARS2), 2210023C10Rik, CGI-04, MLASA2, MT-TYRRS, RGD1311696, tyrRS, TYRRS
Protein level used designations for YARS2
- tyrosine--tRNA ligase, mitochondrial
- tyrosyl-tRNA synthetase, mitochondrial
- tyrosine tRNA ligase 2, mitochondrial