SLC6A5, solute carrier family 6 member 5, 9152

N. diseases: 64; N. variants: 15
Disease: Brain Diseases ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0006111
Disease: Brain Diseases
Brain Diseases 		0.300 Biomarker group CTD_human Molecular basis of the dominant negative effect of a glycine transporter 2 mutation associated with hyperekplexia. 25480793 2015