Homo sapiens phenylalanyl-tRNA synthetase 2, mitochondrial (FARS2), tr - Nucleotide

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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.
Clinical and molecular characterization of novel FARS2 variants causing neonatal mitochondrial disease. [Mol Genet Metab. 2023]
Clinical and molecular characterization of novel FARS2 variants causing neonatal mitochondrial disease.
Chen W, Rehsi P, Thompson K, Yeo M, Stals K, He L, Schimmel P, Chrzanowska-Lightowlers ZMA, Wakeling E, Taylor RW, et al. Mol Genet Metab. 2023 Nov; 140(3):107657. Epub 2023 Jul 24.
TRIM67 drives tumorigenesis in oligodendrogliomas through Rho GTPase-dependent membrane blebbing. [Neuro Oncol. 2023]
TRIM67 drives tumorigenesis in oligodendrogliomas through Rho GTPase-dependent membrane blebbing.
Demirdizen E, Al-Ali R, Narayanan A, Sun X, Varga JP, Steffl B, Brom M, Krunic D, Schmidt C, Schmidt G, et al. Neuro Oncol. 2023 Jun 2; 25(6):1031-1043.

RefSeq alternative splicing
See 25 reference mRNA sequence splice variants for the FARS2 gene.
RefSeq protein product
See the reference protein sequence for phenylalanine--tRNA ligase, mitochondrial isoform 1 (NP_001305801.1).

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Nucleotide