Varaico: Literature-Extracted Genetic Variants

Gene:CYP2C8
Variant:p.R139K
Back to variants list

CYP2C8

NM_000770.3:p.R139K

Associated Papers

Natural Polymorphic Variants in the CYP450 Superfamily: A Review of Potential Structural Mechanisms and Functional Consequences.

Prost R et al.

International Journal of Molecular Sciences, 2025

Genetic and Non-genetic Correlates of Imatinib Pharmacokinetics and Side Effects of Imatinib in Palestinian Patients with Chronic Myeloid Leukemia.

Adawi DH et al.

Biochemical Genetics, 2025

SNP's use as a potential chemotoxicity stratification tool in breast cancer: from bench to clinic.

Moustafa HAM et al.

Functional & Integrative Genomics, 2025

Analgesic therapy failure in a COMT HPS/HPS diplotype carrier heterozygous for the CYP2D6 *4 allele with fibromyalgia-a case report.

Bollinger A et al.

Pain Reports, 2025

39995492 (PubMed )
Supplement: painreports-10-e1248-s001.pdf

Influence of CYP2C8*3 and ABCG2 C421A genetic polymorphisms on trough concentration and molecular response of imatinib in Egyptian patients with chronic myeloid leukemia.

Mangoura SA et al.

Cancer Chemotherapy and Pharmacology, 2024

The Cytochrome P450 2C8*3 Variant (rs11572080) Is Associated with Improved Asthma Symptom Control in Children and Altered Lipid Mediator Production and Inflammatory Response in Human Bronchial Epithelial Cells.

Almestica-Roberts M et al.

Drug Metabolism and Disposition: the Biological Fate of Chemicals, 2024

APF2: an improved ensemble method for pharmacogenomic variant effect prediction.

Zhou Y et al.

The Pharmacogenomics Journal, 2024

38802404 (PubMed )
Supplement: 41397_2024_338_MOESM2_ESM.xlsx › Sheet1

Meta-analysis of the global distribution of clinically relevant CYP2C8 alleles and their inferred functional consequences.

Camara MD et al.

Human Genomics, 2024

CYP2C8 rs11572080 and CYP3A4 rs2740574 risk genotypes in paclitaxel-treated premenopausal breast cancer patients.

Attia HRM et al.

Scientific Reports, 2024

Effect of donor GSTM3 rs7483 genetic variant on tacrolimus elimination in the early period after liver transplantation.

Zhang T et al.

Peerj, 2024

39465171 (PubMed )
Supplement: peerj-12-18360-s002.7z › drug-metabolizing_enzymes_and_transporter__DMET__microarray › markerlist.xlsx › markerlist.TXT

G-quadruplex forming sequences in the genes coding for cytochrome P450 enzymes and their potential roles in drug metabolism.

Saad M et al.

Biochimie, 2023

Functional Characterization of Allelic Variations of Human Cytochrome P450 2C8 (V181I, I244V, I331T, and L361F).

Lee YB et al.

International Journal of Molecular Sciences, 2023

The Influence of Cytochrome P450 Polymorphisms on Pharmacokinetic Profiles and Treatment Outcomes Among Malaria Patients in Sub-Saharan Africa: A Systematic Review.

Marwa KJ et al.

Pharmacogenomics and Personalized Medicine, 2023

Targeted haplotyping in pharmacogenomics using Oxford Nanopore Technologies' adaptive sampling.

Deserranno K et al.

Frontiers in Pharmacology, 2023

38026945 (PubMed )
Supplement: DataSheet1.ZIP › SupplementaryMaterials › SupplementaryMaterials_Tables_S4-S9.xlsx › HG00190_R10.4.1_AldyCalls

Variability of CYP2C8 Polymorphisms in Three Jordanian Populations: Circassians, Chechens and Jordanian-Arabs.

Abudahab S et al.

Journal of Immigrant and Minority Health, 2022

The clinically relevant CYP2C8*3 and CYP2C9*2 haplotype is inherited from Neandertals.

Haeggström S et al.

The Pharmacogenomics Journal, 2022

Diclofenac-induced adverse drug reactions and hyperbilirubinemia caused by a variant gene.

Chen ES et al.

The Kaohsiung Journal of Medical Sciences, 2022

Role of cytochrome P450 2C8 genetic polymorphism and epoxygenase uncoupling in periodontal remodelling affecting orthodontic treatment.

Yamoune S et al.

Basic & Clinical Pharmacology & Toxicology, 2022

Characterization of ADME Gene Variation in Colombian Population by Exome Sequencing.

Silgado-Guzmán DF et al.

Frontiers in Pharmacology, 2022

35846994 (PubMed )
Supplement: Table1.xlsx › Hoja1

Association between gene polymorphisms in the cyclophosphamide metabolism pathway with complications after haploidentical hematopoietic stem cell transplantation.

Muñiz P et al.

Frontiers in Immunology, 2022

36211438 (PubMed )
Supplement: Table_1.xlsx › Hoja1

The impact of IL-10 and CYP3A5 gene polymorphisms on dose-adjusted trough blood tacrolimus concentrations in early post-renal transplant recipients.

Chen Z et al.

Pharmacological Reports : Pr, 2021

Comprehensive analysis of important pharmacogenes in Koreans using the DMET™ platform.

Kim B et al.

Translational and Clinical Pharmacology, 2021

Frequency of Important CYP450 Enzyme Gene Polymorphisms in the Iranian Population in Comparison with Other Major Populations: A Comprehensive Review of the Human Data.

Neyshaburinezhad N et al.

Journal of Personalized Medicine, 2021

34442448 (PubMed )
Supplement: jpm-11-00804-s001.zip › jpm-1270394-supplementary.pdf

Pharmacogenetics of Carbamazepine and Valproate: Focus on Polymorphisms of Drug Metabolizing Enzymes and Transporters.

Iannaccone T et al.

Pharmaceuticals (basel, Switzerland), 2021

Influence of cytochrome P450 (CYP) 2C8 polymorphisms on the efficacy and tolerability of artesunate-amodiaquine treatment of uncomplicated Plasmodium falciparum malaria in Zanzibar.

Pernaute-Lau L et al.

Malaria Journal, 2021

Genetic polymorphisms associated with upper gastrointestinal bleeding: a systematic review.

Forgerini M et al.

The Pharmacogenomics Journal, 2021

Phase II study of eribulin in combination with gemcitabine for the treatment of patients with locally advanced or metastatic triple negative breast cancer (ERIGE trial). Clinical and pharmacogenetic results on behalf of the Gruppo Oncologico Italiano di Ricerca Clinica (GOIRC).

Pellegrino B et al.

Esmo Open, 2021

Exploring pharmacogenetics of paclitaxel- and docetaxel-induced peripheral neuropathy by evaluating the direct pharmacogenetic-pharmacokinetic and pharmacokinetic-neuropathy relationships.

Hertz DL

Expert Opinion on Drug Metabolism & Toxicology, 2021

Development and Analytical Validation of a 29 Gene Clinical Pharmacogenetic Genotyping Panel: Multi-Ethnic Allele and Copy Number Variant Detection.

Scott SA et al.

Clinical and Translational Science, 2021

32931151 (PubMed )
Supplement: CTS-14-204-s001.xlsx › Table_S1

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

Whole-Exome Sequencing in Patients Affected by Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis Reveals New Variants Potentially Contributing to the Phenotype.

Fonseca DJ et al.

Pharmacogenomics and Personalized Medicine, 2021

ABCB1 and ERCC1 gene polymorphisms are associated with nephro- and hepatotoxicity to carboplatin/paclitaxel-based chemotherapy in patients with gynecologic cancers.

da Costa Junior LC et al.

European Journal of Clinical Pharmacology, 2020

Genetic associations of docetaxel-based chemotherapy-induced myelosuppression in Chinese Han population.

Ren W et al.

Journal of Clinical Pharmacy and Therapeutics, 2020

CYP3A5*3 and CYP2C8*3 variants influence exposure and clinical outcomes of tacrolimus-based therapy.

Genvigir FDV et al.

Pharmacogenomics, 2020

Assessment of pharmacogenomic SLCO1B1 assay for prediction of neuromuscular pain in type 2 diabetes mellitus and cardiovascular patients: preliminary results.

Licito A et al.

European Review for Medical and Pharmacological Sciences, 2020

Prevalence of CYP2C8*2 and *3 among Eritreans and its Potential Impact on Artesunate/Amodiaquine Treatment.

Habtemikael L et al.

Pharmacogenomics and Personalized Medicine, 2020

Challenges to assess substrate-dependent allelic effects in CYP450 enzymes and the potential clinical implications.

Marcath LA et al.

The Pharmacogenomics Journal, 2019

Pharmacokinetics/pharmacodynamics of chloroquine and artemisinin-based combination therapy with primaquine.

Daher A et al.

Malaria Journal, 2019

Polymorphisms of CYP2C8 Alter First-Electron Transfer Kinetics and Increase Catalytic Uncoupling.

R Arnold W et al.

International Journal of Molecular Sciences, 2019

Enantiospecific Pharmacogenomics of Fluvastatin.

Hirvensalo P et al.

Clinical Pharmacology and Therapeutics, 2019

30989645 (PubMed )
Supplement: CPT-106-668-s002.pdf

A Variation in the ABCC8 Gene Is Associated with Type 2 Diabetes Mellitus and Repaglinide Efficacy in Chinese Type 2 Diabetes Mellitus Patients.

Zhou X et al.

Internal Medicine (tokyo, Japan), 2019

Impact of gene polymorphisms on the systemic toxicity to paclitaxel/carboplatin chemotherapy for treatment of gynecologic cancers.

de Castro CL et al.

Archives of Gynecology and Obstetrics, 2019

An optimized prediction framework to assess the functional impact of pharmacogenetic variants.

Zhou Y et al.

The Pharmacogenomics Journal, 2019

30206299 (PubMed )
Supplement: 41397_2018_44_MOESM5_ESM.xlsx › Sheet1

Assessment of coding region variants in Kuwaiti population: implications for medical genetics and population genomics.

John SE et al.

Scientific Reports, 2018

Points-to-consider documents: Scientific information on the evaluation of genetic polymorphisms during non-clinical studies and phase I clinical trials in the Japanese population.

Hiratsuka M et al.

Drug Metabolism and Pharmacokinetics, 2018

Pharmacogenomics in Papua New Guineans: unique profiles and implications for enhancing drug efficacy while improving drug safety.

Tucci JD et al.

Pharmacogenetics and Genomics, 2018

1–50 of 189 papers
Select a paper to view details
UCSC Genome Browser·Imprint·Privacy·Terms·Feedback·Email Updates·

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."