Gene: SLC38A8 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 146167
Gene Symbol: SLC38A8
SLC38A8 		0.010 GeneticVariation disease BEFREE Isolated foveal hypoplasia with secondary nystagmus and low vision is associated with a homozygous SLC38A8 mutation. 24045842 2014