Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 84466
Gene Symbol: MEGF10
MEGF10 		0.300 Biomarker disease CTD_human Mutations in MEGF10, a regulator of satellite cell myogenesis, cause early onset myopathy, areflexia, respiratory distress and dysphagia (EMARDD). 22101682 2011
Entrez Id: 283989
Gene Symbol: TSEN54
TSEN54 		0.300 Biomarker disease CTD_human tRNA splicing endonuclease mutations cause pontocerebellar hypoplasia. 18711368 2008
Entrez Id: 79042
Gene Symbol: TSEN34
TSEN34 		0.300 Biomarker disease CTD_human tRNA splicing endonuclease mutations cause pontocerebellar hypoplasia. 18711368 2008
Entrez Id: 80746
Gene Symbol: TSEN2
TSEN2 		0.300 Biomarker disease CTD_human tRNA splicing endonuclease mutations cause pontocerebellar hypoplasia. 18711368 2008