Gene: SLC6A5 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 9152
Gene Symbol: SLC6A5
SLC6A5 		0.500 Biomarker disease CTD_human Molecular basis of the dominant negative effect of a glycine transporter 2 mutation associated with hyperekplexia. 25480793 2015
Entrez Id: 9152
Gene Symbol: SLC6A5
SLC6A5 		0.500 Biomarker disease MGD Deletion of the mouse glycine transporter 2 results in a hyperekplexia phenotype and postnatal lethality. 14622583 2003