Source: CLINGEN

Gene Gene Full Name DSI g DPI g pLI Disease Type Score gda EL gda EI gda N. PMIDs N. SNPs gda First Ref. Last Ref.
Entrez Id: 10667
Gene Symbol: FARS2
FARS2
phenylalanyl-tRNA synthetase 2, mitochondrial 0.615 0.731 9.3E-09
CUI: C0023264
Disease: Leigh Disease
Leigh Disease
disease 0.300 moderate 1.000 7 0 2012 2017
Entrez Id: 10667
Gene Symbol: FARS2
FARS2
phenylalanyl-tRNA synthetase 2, mitochondrial 0.615 0.731 9.3E-09
LEIGH SYNDROME DUE TO MITOCHONDRIAL COMPLEX I DEFICIENCY
disease 0.300 moderate 1.000 7 0 2012 2017
Entrez Id: 10667
Gene Symbol: FARS2
FARS2
phenylalanyl-tRNA synthetase 2, mitochondrial 0.615 0.731 9.3E-09
Leigh Syndrome Due To Mitochondrial Complex II Deficiency
disease 0.300 moderate 1.000 7 0 2012 2017
Entrez Id: 10667
Gene Symbol: FARS2
FARS2
phenylalanyl-tRNA synthetase 2, mitochondrial 0.615 0.731 9.3E-09
Leigh Syndrome due to Mitochondrial Complex III Deficiency
disease 0.300 moderate 1.000 7 0 2012 2017
Entrez Id: 10667
Gene Symbol: FARS2
FARS2
phenylalanyl-tRNA synthetase 2, mitochondrial 0.615 0.731 9.3E-09
Leigh Syndrome due to Mitochondrial Complex IV Deficiency
disease 0.300 moderate 1.000 7 0 2012 2017
Entrez Id: 10667
Gene Symbol: FARS2
FARS2
phenylalanyl-tRNA synthetase 2, mitochondrial 0.615 0.731 9.3E-09
Leigh Syndrome due to Mitochondrial Complex V Deficiency
disease 0.300 moderate 1.000 7 0 2012 2017
Entrez Id: 10667
Gene Symbol: FARS2
FARS2
phenylalanyl-tRNA synthetase 2, mitochondrial 0.615 0.731 9.3E-09
Necrotizing encephalopathy, infantile subacute, of Leigh
disease 0.300 moderate 1.000 7 0 2012 2017