Publication for FARS2 and LYRM4

Species	Symbol	Function*	Entrez Gene ID*	Other ID	Gene coexpression	CoexViewer
hsa	FARS2	phenylalanyl-tRNA synthetase 2, mitochondrial	10667			[link]
hsa	LYRM4	LYR motif containing 4	57128

Pubmed ID	Priority	Text
24161539	0.97	LYRM4 and FARS2, 1both predicted to have a mitochondrial function.
	0.96	LYRM4 gene revealed no known or potentially pathogenic mutations, whilst a novel heterozygous c.973G > T transversion was identified in exon 5 of FARS2, predicting a p.Asp325Tyr amino acid substitution.
	0.92	LYRM4 and FARS2 genes.
	0.90	LYRM4 and FARS2 genes may be, at least in part, responsible for some of the dysmorphic features of the 6p25 deletion syndrome.
	0.89	LYRM4 and FARS2, both of which are partially deleted : the 3' exons of LYRM4 and the regulatory region of the FARS2 gene, including the promoter and untranslated exon 1 (Fig. 2A).
	0.52	LYRM4 encodes a protein required for nuclear and mitochondrial iron-sulphur protein biosynthesis, whilst FARS2 encodes the mitochondrial phenylalanyl-tRNA synthetase.
26174853	0.89	LYRM4, FARS2, NRN1, F13A1, LY86, RREB1, SSR1, CAGE1, DSP, BMP6, BLOC1S5, EEF1E1, SLC35B3, HULC and OFCC1) and 10 other genes (PPP1R3G, LY86-AS1, SNAPC5P1, CNN3P1, BTF3P7, RIOK1, SNRNP48, TXNDC5, BLOC1S5-TXNDC5 and PIP5K1P1).