Gene: SLC22A5 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 6584
Gene Symbol: SLC22A5
SLC22A5 		0.010 GeneticVariation disease BEFREE DNA sequencing analysis disclosed a missense mutation from CTG (Leu) to CGG (Arg) at codon 352 located within the sixth transmembrane domain of octn2. 9837751 1998