phenylalanine--tRNA ligase, mitochondrial isoform X1 [Rattus norvegicu - Protein

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A Newly Identified Missense Mutation in FARS2 Causes Autosomal-Recessive Spastic Paraplegia. [Hum Mutat. 2016]
A Newly Identified Missense Mutation in FARS2 Causes Autosomal-Recessive Spastic Paraplegia.
Yang Y, Liu W, Fang Z, Shi J, Che F, He C, Yao L, Wang E, Wu Y. Hum Mutat. 2016 Feb; 37(2):165-9. Epub 2015 Dec 10.
Expression and characterization of a human mitochondrial phenylalanyl-tRNA synthetase. [J Mol Biol. 1999]
Expression and characterization of a human mitochondrial phenylalanyl-tRNA synthetase.
Bullard JM, Cai YC, Demeler B, Spremulli LL. J Mol Biol. 1999 May 14; 288(4):567-77.
FARS2 Deficiency Causes Cardiomyopathy by Disrupting Mitochondrial Homeostasis and the Mitochondrial Quality Control System. [Circulation. 2024]
FARS2 Deficiency Causes Cardiomyopathy by Disrupting Mitochondrial Homeostasis and the Mitochondrial Quality Control System.
Li B, Liu F, Chen X, Chen T, Zhang J, Liu Y, Yao Y, Hu W, Zhang M, Wang B, et al. Circulation. 2024 Apr 16; 149(16):1268-1284. Epub 2024 Feb 16.

RefSeq mRNA
See reference mRNA sequence for the Fars2 gene (XM_006253823.5).
RefSeq protein isoforms
See 21 reference sequence protein isoforms for the Fars2 gene.

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Protein