Gene-drug interactions (data source: DGIdb)
Gene Name Entrez ID Drug Name Chembl ID Interaction Types Sources publications
SLC22A5 6584 LEVOCARNITINE CHEMBL1149 DrugBank 12181285, 12183691, 12644265, 12175785, 12635840

Variant-drug associations (data source: PharmGKB)
Gene Name Variant Alleles Chemical Phenotype Category Significance Notes Sentence Publications Annotation ID
SLC22A5 rs2631372 CG + GG imatinib efficacy yes Carriers of the G allele had prolonged time to progression, which was calculated from the start of therapy to the date of disease progression as documented by a CT scan performed every 3-4 months. Genotypes CG + GG are associated with increased response to imatinib in people with Gastrointestinal Stromal Tumors as compared to genotype CC. 23127916 982046735
SLC22A5 rs2631367 CG + GG imatinib efficacy yes Carriers of the G allele had prolonged time to progression, which was calculated from the start of therapy to the date of disease progression as documented by a CT scan performed every 3-4 months. Genotypes CG + GG are associated with increased response to imatinib in people with Gastrointestinal Stromal Tumors as compared to genotype CC. 23127916 982046731
SLC22A5 rs2631372 G imatinib dosage no No significant association between genotype and chance of requiring an imatinib dose reduction. Allele G is not associated with dose of imatinib in people with Gastrointestinal Stromal Tumors as compared to allele C. 30713339 1450933302
SLC22A5 rs2631367 C imatinib dosage no No significant association between genotype and chance of requiring an imatinib dose reduction. Allele C is not associated with dose of imatinib in people with Gastrointestinal Stromal Tumors as compared to allele G. 30713339 1450933253
SLC22A5 rs2631370 C imatinib dosage no No significant association between genotype and chance of requiring an imatinib dose reduction. Allele C is not associated with dose of imatinib in people with Gastrointestinal Stromal Tumors as compared to allele T. 30713339 1450933294