Gene: TRNL2 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4568
Gene Symbol: TRNL2
TRNL2 		0.100 CausalMutation disease CLINVAR Pathogenic mitochondrial tRNA mutations--which mutations are inherited and why? 19718780 2009
Entrez Id: 4568
Gene Symbol: TRNL2
TRNL2 		0.100 CausalMutation disease CLINVAR Identification of novel mutations in five patients with mitochondrial encephalomyopathy. 18977334 2009
Entrez Id: 4568
Gene Symbol: TRNL2
TRNL2 		0.100 CausalMutation disease CLINVAR Mitochondrial myopathy and ophthalmoplegia in a sporadic patient with the G12315A mutation in mitochondrial DNA. 12398839 2002
Entrez Id: 4568
Gene Symbol: TRNL2
TRNL2 		0.100 CausalMutation disease CLINVAR Complete restoration of a wild-type mtDNA genotype in regenerating muscle fibres in a patient with a tRNA point mutation and mitochondrial encephalomyopathy. 9361028 1997
Entrez Id: 4568
Gene Symbol: TRNL2
TRNL2 		0.100 CausalMutation disease CLINVAR A novel heteroplasmic tRNAleu(CUN) mtDNA point mutation in a sporadic patient with mitochondrial encephalomyopathy segregates rapidly in skeletal muscle and suggests an approach to therapy. 8923013 1996