Gene: TRNE ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4556
Gene Symbol: TRNE
TRNE 		0.110 GeneticVariation phenotype BEFREE Early-onset cataracts, spastic paraparesis, and ataxia caused by a novel mitochondrial tRNAGlu (MT-TE) gene mutation causing severe complex I deficiency: a clinical, molecular, and neuropathologic study. 23334599 2013
Entrez Id: 4556
Gene Symbol: TRNE
TRNE 		0.110 Biomarker phenotype HPO