Varaico: Literature-Extracted Genetic Variants

Gene:SLC22A1
Variant:p.G465R
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SLC22A1

NM_003057.3:p.G465R

Associated Papers

The divergent roles of tryptophans W354 and W217 in OCT1 transport: Similar localization, distinct functions.

Römer S et al.

The Journal of Biological Chemistry, 2025

Characterisation of pharmacogenomic variation in the Shetland and Orkney Isles in Scotland.

Twesigomwe D et al.

Scientific Reports, 2025

Genetic Variants of SLC22A1 rs628031 and rs622342 and Glycemic Control in T2DM Patients from Northern Mexico.

Moreno-González JG et al.

Genes, 2025

Sex-Dependent Effects of CYP2D6 on the Pharmacokinetics of Berberine in Humans.

Blöcher JA et al.

Clinical Pharmacology and Therapeutics, 2025

Insights Into Genetic Variations of the OCT1 Gene in Metformin Poor Responders Among Bangladeshi Type 2 Diabetic Patients.

Begum R et al.

Advances in Pharmacological and Pharmaceutical Sciences, 2025

Metformin efficacy and tolerance according to genetic polymorphisms of organic cation transporter 1 in Tunisian patients with type 2 diabetes.

Chaker F et al.

Frontiers in Endocrinology, 2025

Effect of SLC22A1 polymorphism on the pharmacokinetics of proguanil in Korean: A semi-physiologic population pharmacokinetic approach.

Khwarg J et al.

Clinical and Translational Science, 2024

Effects of genetic variants of organic cation transporters on metformin response in newly diagnosed patients with type 2 diabetes.

AlKreathy HM et al.

Medicine, 2024

The full spectrum of SLC22 OCT1 mutations illuminates the bridge between drug transporter biophysics and pharmacogenomics.

Yee SW et al.

Molecular Cell, 2024

Structural insights into human organic cation transporter 1 transport and inhibition.

Zhang S et al.

Cell Discovery, 2024

Landscape of pharmacogenetic variants associated with non-insulin antidiabetic drugs in the Indian population.

Sivadas A et al.

Bmj Open Diabetes Research & Care, 2024

38471670 (PubMed )
Supplement: bmjdrc-2023-003769supp001.pdf

Influence of Solute Carrier Family 22 Member 1 (SLC22A1) Gene Polymorphism on Metformin Pharmacokinetics and HbA1c Levels: A Systematic Review.

Pradana AD et al.

Current Diabetes Reviews, 2024

The polygenic implication of clopidogrel responsiveness: Insights from platelet reactivity analysis and next-generation sequencing.

Echeverría O et al.

Plos One, 2024

38991024 (PubMed )
Supplement: pone.0306445.s008.xlsx › Supplementary_Table_6

Association of SLC22A1, SLC47A1, and KCNJ11 polymorphisms with efficacy and safety of metformin and sulfonylurea combination therapy in Egyptian patients with type 2 diabetes.

Ahmed A et al.

Research in Pharmaceutical Sciences, 2023

The full spectrum of OCT1 (SLC22A1) mutations bridges transporter biophysics to drug pharmacogenomics.

Yee SW et al.

Biorxiv : the Preprint Server for Biology, 2023

The Role of Organic Cation Transporters in the Pharmacokinetics, Pharmacodynamics and Drug-Drug Interactions of Tyrosine Kinase Inhibitors.

Xiu F et al.

International Journal of Molecular Sciences, 2023

Rescue of Misfolded Organic Cation Transporter 3 Variants.

Angenoorth TJF et al.

Cells, 2022

Hepatic solute carrier transporters and drug therapy: Regulation of expression and impact of genetic variation.

Nies AT et al.

Pharmacology & Therapeutics, 2022

Activated leukocyte cell adhesion molecule/cluster of differentiation 166 rs10933819 (G>A) variant is associated with familial intracranial aneurysms.

Aitkulova A et al.

Biomedical Reports, 2022

35815187 (PubMed )
Supplement: Supplementary_Data.xlsx › 713_shortlisted_variants

Population pharmacogenomics: an update on ethnogeographic differences and opportunities for precision public health.

Zhou Y et al.

Human Genetics, 2022

Genetic Variant ABCC1 rs45511401 Is Associated with Increased Response to Statins in Patients with Familial Hypercholesterolemia.

Dagli-Hernandez C et al.

Pharmaceutics, 2022

35631530 (PubMed )
Supplement: pharmaceutics-14-00944-s001.zip › pharmaceutics-1634615-supplementary.pdf

No significant influence of OCT1 genotypes on the pharmacokinetics of morphine in adult surgical patients.

Kuhlmann I et al.

Basic & Clinical Pharmacology & Toxicology, 2022

Emerging Roles of the Human Solute Carrier 22 Family.

Yee SW et al.

Drug Metabolism and Disposition: the Biological Fate of Chemicals, 2021

Characterization of cytochrome P450 (CYP) 2D6 drugs as substrates of human organic cation transporters and multidrug and toxin extrusion proteins.

Neul C et al.

British Journal of Pharmacology, 2021

Decoding variants in drug-metabolizing enzymes and transporters in solid tumor patients by whole-exome sequencing.

Aboul-Soud MAM et al.

Saudi Journal of Biological Sciences, 2021

33424349 (PubMed )
Supplement: mmc1.xlsx › Sheet1

Diabetes and Genetics: A Relationship Between Genetic Risk Alleles, Clinical Phenotypes and Therapeutic Approaches.

Sayed S et al.

Advances in Experimental Medicine and Biology, 2021

Expansion of Knowledge on OCT1 Variant Activity In Vitro and In Vivo Using Oct1/2-/- Mice.

Morse BL et al.

Frontiers in Pharmacology, 2021

Effects of a Common Eight Base Pairs Duplication at the Exon 7-Intron 7 Junction on Splicing, Expression, and Function of OCT1.

Römer S et al.

Frontiers in Pharmacology, 2021

Isobutyrylcarnitine as a Biomarker of OCT1 Activity and Interspecies Differences in its Membrane Transport.

Jensen O et al.

Frontiers in Pharmacology, 2021

Effects of Genetic Polymorphism in CYP2D6, CYP2C19, and the Organic Cation Transporter OCT1 on Amitriptyline Pharmacokinetics in Healthy Volunteers and Depressive Disorder Patients.

Matthaei J et al.

Frontiers in Pharmacology, 2021

The Genetics of Adverse Drug Outcomes in Type 2 Diabetes: A Systematic Review.

Baye AM et al.

Frontiers in Genetics, 2021

The Impact of Genetic Polymorphisms in Organic Cation Transporters on Renal Drug Disposition.

Zazuli Z et al.

International Journal of Molecular Sciences, 2020

Genetic Diversity in Drug Transporters: Impact in African Populations.

Rajman I et al.

Clinical and Translational Science, 2020

Influence of MRP3 Genetics and Hepatic Expression Ontogeny for Morphine Disposition in Neonatal and Pediatric Patients.

Hahn D et al.

Journal of Clinical Pharmacology, 2020

Sorafenib Resistance in Hepatocellular Carcinoma: The Relevance of Genetic Heterogeneity.

Cabral LKD et al.

Cancers, 2020

Role of Genetic Variations in the Hepatic Handling of Drugs.

Marin JJG et al.

International Journal of Molecular Sciences, 2020

Variability and Heritability of Thiamine Pharmacokinetics With Focus on OCT1 Effects on Membrane Transport and Pharmacokinetics in Humans.

Jensen O et al.

Clinical Pharmacology and Therapeutics, 2020

Oncology and Pharmacogenomics Insights in Polycystic Ovary Syndrome: An Integrative Analysis.

Yumiceba V et al.

Frontiers in Endocrinology, 2020

Cellular Uptake of Psychostimulants - Are High- and Low-Affinity Organic Cation Transporters Drug Traffickers?

Jensen O et al.

Frontiers in Pharmacology, 2020

Diffusion Mechanism Modeling of Metformin in Human Organic Cationic Amino Acid Transporter one and Functional Impact of S189L, R206C, and G401S Mutation.

Cano L et al.

Frontiers in Pharmacology, 2020

The genetic landscape of the human solute carrier (SLC) transporter superfamily.

Schaller L et al.

Human Genetics, 2019

Opioids as Substrates and Inhibitors of the Genetically Highly Variable Organic Cation Transporter OCT1.

Meyer MJ et al.

Journal of Medicinal Chemistry, 2019

Targeted next generation sequencing as a tool for precision medicine.

Gulilat M et al.

Bmc Medical Genomics, 2019

31159795 (PubMed )
Supplement: 12920_2019_527_MOESM1_ESM.xlsx › Table_S6
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Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."