EC Number |
Disease |
PubMed ID |
Title of Publication |
Category |
Confidence Level |
---|
6.1.1.9 | Brain Diseases |
30755602 |
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 |
30755616 |
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 |
33937156 |
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 |
30755616 |
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 |
33937156 |
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 |
330535 |
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 |
3881597 |
Response of a phage modification factor to enhanced production of its target molecule. |
unassigned |
0 |
6.1.1.9 | Infections |
20668681 |
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 |
837925 |
Subcellular distribution of aminoacyl-tRNA synthetases in various eukaryotic cells. |
diagnostic usage unassigned |
1 0 |
6.1.1.9 | Leukemia |
9461376 |
Evolutionary significance of intra-genome duplications on human chromosomes. |
unassigned |
0 |