Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 10943
Gene Symbol: MSL3
MSL3 		0.300 Biomarker phenotype CTD_human De novo mutations in MSL3 cause an X-linked syndrome marked by impaired histone H4 lysine 16 acetylation. 30224647 2018
Entrez Id: 6647
Gene Symbol: SOD1
SOD1 		0.300 Biomarker phenotype CTD_human Bromocriptine methylate suppresses glial inflammation and moderates disease progression in a mouse model of amyotrophic lateral sclerosis. 21867702 2011
Entrez Id: 54902
Gene Symbol: TTC19
TTC19 		0.300 Biomarker phenotype CTD_human Mutations in TTC19 cause mitochondrial complex III deficiency and neurological impairment in humans and flies. 21278747 2011
Entrez Id: 3897
Gene Symbol: L1CAM
L1CAM 		0.300 Biomarker phenotype CTD_human MASA syndrome is due to mutations in the neural cell adhesion gene L1CAM. 7920660 1994