Gene-drug interactions (data source: DGIdb)
Gene Name Entrez ID Drug Name Chembl ID Interaction Types Sources publications
TLR4 7099 ALCOHOL CHEMBL545 NCI 11431739
TLR4 7099 SAQUINAVIR CHEMBL114 NCI 15388451
TLR4 7099 DODECANOATE CHEMBL108766 DrugBank 10592235
TLR4 7099 MYRISTIC ACID CHEMBL111077 DrugBank 10592235
TLR4 7099 CHEMBL225157 CHEMBL225157 antagonist GuideToPharmacologyInteractions, TTD
TLR4 7099 ERITORAN TETRASODIUM (CHEMBL3301672) CHEMBL3301672 antagonist ChemblInteractions
TLR4 7099 CHEMBL1232858 CHEMBL1232858 DrugBank 10592235
TLR4 7099 GOLOTIMOD CHEMBL2103812 DrugBank
TLR4 7099 NELFINAVIR CHEMBL584 NCI 15388451
TLR4 7099 RITONAVIR CHEMBL163 NCI 15388451
TLR4 7099 FOLIC ACID CHEMBL1622 PharmGKB
TLR4 7099 INFLIXIMAB CHEMBL1201581 NCI 12847679
TLR4 7099 ERITORAN (CHEMBL501259) CHEMBL501259 TdgClinicalTrial, DrugBank 17803912, 16820585

Variant-drug associations (data source: PharmGKB)
Gene Name Variant Alleles Chemical Phenotype Category Significance Notes Sentence Publications Annotation ID
TLR4 rs4986790 AA Pertussis vaccines efficacy yes 10-year follow-up for a booster dose of acellular pertussis vaccine. Original vaccine given at 3, 4, 5 and 24 months old. No pertussis had occurred in any patients at this 10-year point. The fold increase in antibody response to pertussis toxin after vaccination was significantly lower in subjects with the AG or GG genotypes as compared to those with the AA genotype (wild-type); 55% vs 86%, respectively. Genotype AA is associated with increased response to Pertussis vaccines in children as compared to genotypes AG + GG. 22383676 1444702987
TLR4 TLR4 haplotype tacrolimus metabolism/PK yes The poor metabolizer group consisted of 1) recipients with genotype CC at rs776746 (CYP3A5) with livers from 2) donors with a genotype of CC at rs776746 (CYP3A5) and a genotype of CC at rs1927907 (TLR4). The extensive metabolizer group consisted of 1) recipients with a rs776746 (CYP3A4) TT/CT genotype with livers from 2) donors with a genotype of TT/CT at rs776746 (CYP3A5) and a genotype of TT/CT at rs1927907 (TLR4). The intermediate metabolizer groups consisted of other genotype combinations at rs776746 and rs1927907. TLR4 poor metabolizer genotype is associated with increased concentrations of tacrolimus in people with liver transplantation as compared to TLR4 intermediate metabolizer and normal metabolizer. 24820765 1184754633
TLR4 rs2770150 GG Pertussis vaccines efficacy yes Patients with the GG genotype had a lower pertussis toxin-specific immunoglobulin G (PT-IgG) titer following whole-cell pertussis vaccination as compared to those with the AG genotype. The IgG antibody titer against PT correlates with protection against disease. Please note alleles have been complemented to the plus chromosomal strand. Genotype GG is associated with decreased response to Pertussis vaccines in children as compared to genotype AG. 17699831 1444702155
TLR4 rs5030728 AA + AG Tumor necrosis factor alpha efficacy yes Cohort with inflammatory bowel disease (IBD). Subcohorts with Crohn's disease (CD) and ulcerative colitis (UC) were also analyzed. Significant results for this genotype seen for all cohorts. Treatment efficacy was defined using the three-step scale (failure, response, or remission) and reflected the maximum response within 22 weeks after treatment initiation. Genotypes AA + AG is associated with increased response to Tumor necrosis factor alpha (TNF-alpha) inhibitors in people with Inflammatory Bowel Diseases as compared to genotype GG. 24776844 1296666768
TLR4 rs1927907 T tacrolimus metabolism/PK no This study was attempting to validate reported variants and tacrolimus trough concentration in a large population of African American and European American kidney transplant patients. Allele T is not associated with trough concentration of tacrolimus in people with Kidney Transplantation and Transplantation as compared to allele C. 29318894 1449163120
TLR4 rs1927907 CC tacrolimus metabolism/PK yes The genotype of liver transplant donors as well as the genotype of liver transplant recipients was evaluated for its effect on dose adjusted trough concentration of tacrolimus on recipients. The CT+TT genotype of donors was associated with significantly lower dose adjusted trough concentrations of tacrolimus as compared to the CC genotype. The genotype of the donor was not associated with dose adjusted trough concentration of tacrolimus in the recipient. Genotype CC is associated with increased concentrations of tacrolimus in people with liver transplantation as compared to genotypes CT + TT. 24820765 1184754606