tryptophan--tRNA ligase, mitochondrial isoform 7 [Homo sapiens]

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WARS2 Deficiency. [GeneReviews(®). 1993]
WARS2 Deficiency.
Mroczek M, Busra A, Houlden H, Efthymiou S, Nagy S. GeneReviews(®). 1993-2024. 2023 Oct 12
The Expanding Phenotypical Spectrum of WARS2-Related Disorder: Four Novel Cases with a Common Recurrent Variant. [Genes (Basel). 2023]
The Expanding Phenotypical Spectrum of WARS2-Related Disorder: Four Novel Cases with a Common Recurrent Variant.
Pauly MG, Korenke GC, Diaw SH, Grözinger A, Cazurro-Gutiérrez A, Pérez-Dueñas B, González V, Macaya A, Serrano Antón AT, Peterlin B, et al. Genes (Basel). 2023 Mar 29; 14(4). Epub 2023 Mar 29.
A relatively common hypomorphic variant in WARS2 causes monogenic disease. [Parkinsonism Relat Disord. 2022]
A relatively common hypomorphic variant in WARS2 causes monogenic disease.
Ilinca A, Kafantari E, Puschmann A. Parkinsonism Relat Disord. 2022 Jan; 94:129-131. Epub 2022 Jan 19.

RefSeq genomic sequence
See the genomic reference sequence for the WARS2 gene (NG_050658.1).
RefSeq mRNA
See reference mRNA sequence for the WARS2 gene (NM_001378231.1).

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Protein