6.1.1.9 Brain Diseases http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=30755602&form=6&db=m Biallelic mutations in valyl-tRNA synthetase gene VARS are associated with a progressive neurodevelopmental epileptic encephalopathy. causal interaction,unassigned 3,0 6.1.1.9 Brain Diseases http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=30755616&form=6&db=m Biallelic VARS variants cause developmental encephalopathy with microcephaly that is recapitulated in vars knockout zebrafish. ongoing research,therapeutic application,unassigned 1,1,0 6.1.1.9 Cardiomyopathy, Hypertrophic http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=33937156&form=6&db=m Case Report and Review of the Literature: A New and a Recurrent Variant in the VARS2 Gene Are Associated With Isolated Lethal Hypertrophic Cardiomyopathy, Hyperlactatemia, and Pulmonary Hypertension in Early Infancy. causal interaction,unassigned 4,0 6.1.1.9 Epilepsy http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=30755616&form=6&db=m Biallelic VARS variants cause developmental encephalopathy with microcephaly that is recapitulated in vars knockout zebrafish. ongoing research,therapeutic application,unassigned 1,1,0 6.1.1.9 Epilepsy http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=33937156&form=6&db=m Case Report and Review of the Literature: A New and a Recurrent Variant in the VARS2 Gene Are Associated With Isolated Lethal Hypertrophic Cardiomyopathy, Hyperlactatemia, and Pulmonary Hypertension in Early Infancy. causal interaction,unassigned 4,0 6.1.1.9 Infections http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=330535&form=6&db=m Analysis of the structure of T4 bacteriophage-modified valyl-tRNA synthetase by limited proteolysis and isoelectric focusing. therapeutic application,unassigned 2,0 6.1.1.9 Infections http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=3881597&form=6&db=m Response of a phage modification factor to enhanced production of its target molecule. unassigned - 6.1.1.9 Infections http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=20668681&form=6&db=m C. elegans germline-deficient mutants respond to pathogen infection using shared and distinct mechanisms. causal interaction,diagnostic usage,therapeutic application,unassigned 1,3,2,0 6.1.1.9 Leukemia http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=837925&form=6&db=m Subcellular distribution of aminoacyl-tRNA synthetases in various eukaryotic cells. diagnostic usage,unassigned 1,0 6.1.1.9 Leukemia http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=9461376&form=6&db=m Evolutionary significance of intra-genome duplications on human chromosomes. unassigned - 6.1.1.9 Liver Neoplasms, Experimental http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=4373889&form=6&db=m [Effects of ionizing radiations on the activity of valyl-tRNA synthetase isolated from rat liver and Morris hepatoma 7777 (author's transl)] ongoing research,unassigned 4,0 6.1.1.9 Microcephaly http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=29691655&form=6&db=m Loss of function mutations in VARS encoding cytoplasmic valyl-tRNA synthetase cause microcephaly, seizures, and progressive cerebral atrophy. causal interaction,unassigned 4,0 6.1.1.9 Microcephaly http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=30755616&form=6&db=m Biallelic VARS variants cause developmental encephalopathy with microcephaly that is recapitulated in vars knockout zebrafish. ongoing research,therapeutic application,unassigned 1,1,0 6.1.1.9 Muscle Hypotonia http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=33937156&form=6&db=m Case Report and Review of the Literature: A New and a Recurrent Variant in the VARS2 Gene Are Associated With Isolated Lethal Hypertrophic Cardiomyopathy, Hyperlactatemia, and Pulmonary Hypertension in Early Infancy. causal interaction,unassigned 4,0 6.1.1.9 Neoplasms http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=30381327&form=6&db=m Identification of a Specific Translational Machinery via TCTP-EF1A2 Interaction Regulating NF1-associated Tumor Growth by Affinity Purification and Data-independent Mass Spectrometry Acquisition (AP-DIA). unassigned - 6.1.1.9 Seizures http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=29691655&form=6&db=m Loss of function mutations in VARS encoding cytoplasmic valyl-tRNA synthetase cause microcephaly, seizures, and progressive cerebral atrophy. causal interaction,unassigned 4,0 6.1.1.9 Sjogren's Syndrome http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=9218536&form=6&db=m Short-range linkage relationships of the valyl-tRNA synthetase gene in Fugu rubripes. therapeutic application,unassigned 1,0 6.1.1.9 Tuberculosis http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=6788678&form=6&db=m Purification & properties of valyl-tRNA synthetase from Mycobacterium tuberculosis H37Rv. ongoing research,unassigned 3,0