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 		0.420 Biomarker phenotype 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 		0.420 GeneticVariation phenotype BEFREE Patients with SLC6A5 mutations were significantly more likely to have had recurrent infantile apnoeas (RR1.9; P < 0.005) than those with GLRA1 mutations. 24030948 2013
Entrez Id: 9152
Gene Symbol: SLC6A5
SLC6A5 		0.420 GeneticVariation phenotype BEFREE Genotype-phenotype analysis revealed a high rate of neonatal apneas and learning difficulties associated with SLC6A5 mutations. 22700964 2012
Entrez Id: 9152
Gene Symbol: SLC6A5
SLC6A5 		0.420 Biomarker phenotype HPO