Gene: SCYL1 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 57410
Gene Symbol: SCYL1
SCYL1 		0.110 GeneticVariation phenotype BEFREE Previously, we discovered the disruption of Scyl1 as the molecular basis of the mouse mutant mdf, which is affected by neurogenic muscular atrophy, progressive gait ataxia with tremor, cerebellar vermis atrophy, and optic-nerve thinning. 26581903 2015
Entrez Id: 57410
Gene Symbol: SCYL1
SCYL1 		0.110 Biomarker phenotype HPO