Gene: KARS1 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 3735
Gene Symbol: KARS1
KARS1 		0.110 Biomarker phenotype BEFREE Mutations in the KARS gene, which encodes both the cytosolic and mitochondrial isoform of lysyl-tRNA synthetase, cause predominantly neurological diseases that often involve deafness, but have also been linked to cardiomyopathy, developmental delay, and lactic acidosis. 30252186 2018
Entrez Id: 3735
Gene Symbol: KARS1
KARS1 		0.110 CausalMutation phenotype CLINVAR