CD14, CD14 molecule, 929

N. diseases: 551; N. variants: 8
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2569190
rs2569190
Entrez Id: 929;55374
Gene Symbol: CD14;TMCO6
CD14;TMCO6
CUI: C0566602
Disease:
Primary sclerosing cholangitis
0.010 GeneticVariation BEFREE PSC and LTx cohort patients and primary biliary cirrhosis (PBC) control patients were genotyped for the CD14 -260C>T (rs2569190) polymorphism, and genotypes were correlated with long-term clinical outcome. 26970220 2016
dbSNP: rs2569190
rs2569190
Entrez Id: 929;55374
Gene Symbol: CD14;TMCO6
CD14;TMCO6
CUI: C0858617
Disease:
Posterior subcapsular cataract
0.010 GeneticVariation BEFREE PSC and LTx cohort patients and primary biliary cirrhosis (PBC) control patients were genotyped for the CD14 -260C>T (rs2569190) polymorphism, and genotypes were correlated with long-term clinical outcome. 26970220 2016
dbSNP: rs2569190
rs2569190
Entrez Id: 929;55374
Gene Symbol: CD14;TMCO6
CD14;TMCO6
CUI: C3662483
Disease:
Allergic sensitization
0.010 GeneticVariation BEFREE A borderline significant multiplicative interaction was found between E coli and the rs2569190 (CD14/-159) SNP regarding allergic sensitization. 20109750 2010
dbSNP: rs2569190
rs2569190
Entrez Id: 929;55374
Gene Symbol: CD14;TMCO6
CD14;TMCO6
CUI: C0010054
Disease:
Coronary Arteriosclerosis
0.010 GeneticVariation BEFREE Association of COL4A1 (rs605143, rs565470) and CD14 (rs2569190) genes polymorphism with coronary artery disease. 29299748 2018
dbSNP: rs2569190
rs2569190
Entrez Id: 929;55374
Gene Symbol: CD14;TMCO6
CD14;TMCO6
CUI: C0010068
Disease:
Coronary heart disease
0.010 GeneticVariation BEFREE Association of COL4A1 (rs605143, rs565470) and CD14 (rs2569190) genes polymorphism with coronary artery disease. 29299748 2018
dbSNP: rs2569190
rs2569190
Entrez Id: 929;55374
Gene Symbol: CD14;TMCO6
CD14;TMCO6
CUI: C4554344
Disease:
IgE-mediated food allergy
0.010 GeneticVariation BEFREE Development of FA was associated with longer periods of breastfeeding (adjusted OR = 1.792, P = .03), and this dietary pattern was more significantly related to the development of FA in infants with the homozygous TT genotype of CD14 (rs2569190) and more than 1 copy of GSTM1 and GSTT1. 30930272 2019
dbSNP: rs2569191
rs2569191
Entrez Id: 929;55374
Gene Symbol: CD14;TMCO6
CD14;TMCO6
CUI: C0264408
Disease:
Childhood asthma
0.010 GeneticVariation BEFREE Four SNPs, rs2569191 (-1145GA), rs5744455 (-550CT or -651CT), rs2569190 (-159CT or -260CT), and rs4914 in CD14 were genotyped in 762 children from the Environmental and Childhood Asthma study. 20398919 2010
dbSNP: rs5744455
rs5744455
Entrez Id: 929;55374
Gene Symbol: CD14;TMCO6
CD14;TMCO6
CUI: C0264408
Disease:
Childhood asthma
0.010 GeneticVariation BEFREE Four SNPs, rs2569191 (-1145GA), rs5744455 (-550CT or -651CT), rs2569190 (-159CT or -260CT), and rs4914 in CD14 were genotyped in 762 children from the Environmental and Childhood Asthma study. 20398919 2010
dbSNP: rs2569190
rs2569190
Entrez Id: 929;55374
Gene Symbol: CD14;TMCO6
CD14;TMCO6
CUI: C0264408
Disease:
Childhood asthma
0.010 GeneticVariation BEFREE Four SNPs, rs2569191 (-1145GA), rs5744455 (-550CT or -651CT), rs2569190 (-159CT or -260CT), and rs4914 in CD14 were genotyped in 762 children from the Environmental and Childhood Asthma study. 20398919 2010
dbSNP: rs4914
rs4914
Entrez Id: 929;55374
Gene Symbol: CD14;TMCO6
CD14;TMCO6
CUI: C0264408
Disease:
Childhood asthma
0.010 GeneticVariation BEFREE Four SNPs, rs2569191 (-1145GA), rs5744455 (-550CT or -651CT), rs2569190 (-159CT or -260CT), and rs4914 in CD14 were genotyped in 762 children from the Environmental and Childhood Asthma study. 20398919 2010
dbSNP: rs2569190
rs2569190
Entrez Id: 929;55374
Gene Symbol: CD14;TMCO6
CD14;TMCO6
CUI: C1719672
Disease:
Severe Sepsis
0.010 GeneticVariation BEFREE Genotypes GG of rs2569190 (the CD14 gene) and AT of rs4073 (the IL8 gene) were associated with a significantly increased risk of developing severe sepsis (p = 0.05 and p = 0.01). 25000179 2014
dbSNP: rs2569190
rs2569190
Entrez Id: 929;55374
Gene Symbol: CD14;TMCO6
CD14;TMCO6
CUI: C2607914
Disease:
Allergic rhinitis (disorder)
0.010 GeneticVariation BEFREE However, the accumulating evidence does not support an association of IL-13 SNP rs1800925 and CD14 SNP rs2569190 with AR risk. 29687183 2018
dbSNP: rs2569190
rs2569190
Entrez Id: 929;55374
Gene Symbol: CD14;TMCO6
CD14;TMCO6
CUI: C0035243
Disease:
Respiratory Tract Infections
0.010 GeneticVariation BEFREE In children with TT genotype at rs2569190, a higher prenatal intake of vitamins A and C, fruits, and total FV decreased RTI risk (P-trend <0.05), while in infants with TC+CC genotype, a higher prenatal intake of fruit increased RTI risk (P-trend <0.05). 27830580 2017
dbSNP: rs2569190
rs2569190
Entrez Id: 929;55374
Gene Symbol: CD14;TMCO6
CD14;TMCO6
CUI: C0036690
Disease:
Septicemia
0.020 GeneticVariation BEFREE In conclusion, CD14 rs2569190 may act as a prognostic variable for the short-term outcome (30-day survival) in patients with sepsis. 26020644 2015
dbSNP: rs2569190
rs2569190
Entrez Id: 929;55374
Gene Symbol: CD14;TMCO6
CD14;TMCO6
CUI: C0243026
Disease:
Sepsis
0.020 GeneticVariation BEFREE In conclusion, CD14 rs2569190 may act as a prognostic variable for the short-term outcome (30-day survival) in patients with sepsis. 26020644 2015
dbSNP: rs2569190
rs2569190
Entrez Id: 929;55374
Gene Symbol: CD14;TMCO6
CD14;TMCO6
CUI: C0013595
Disease:
Eczema
0.010 GeneticVariation BEFREE In dominant models adjusted for potential confounders, SNP rs2569193 was associated with significantly decreased risk for eczema (odds ratio [OR] for CT/TT vs CC, 0.5; 95% CI, 0.3-0.8), whereas SNP rs2569190 (also reported as the C-159T) was associated with significantly increased risk for eczema (OR for CT/TT vs CC, 2.3; 95% CI, 1.4-3.8). 15867866 2005
dbSNP: rs2569190
rs2569190
Entrez Id: 929;55374
Gene Symbol: CD14;TMCO6
CD14;TMCO6
CUI: C0018213
Disease:
Graves Disease
0.010 GeneticVariation BEFREE In genetic model analysis, the allele model, recessive model, and homozygous model of rs2569190 and rs2915863 embodied strong correlations with GD after the adjusting of age and gender (<i>P</i> = 0.014, <i>P</i> = 0.015, <i>P</i> = 0.009, and <i>P</i> = 0.014, <i>P</i> = 0.001, <i>P</i> = 0.006, respectively). 30700980 2018
dbSNP: rs2915863
rs2915863
Entrez Id: 929;55374
Gene Symbol: CD14;TMCO6
CD14;TMCO6
CUI: C0018213
Disease:
Graves Disease
0.010 GeneticVariation BEFREE In genetic model analysis, the allele model, recessive model, and homozygous model of rs2569190 and rs2915863 embodied strong correlations with GD after the adjusting of age and gender (<i>P</i> = 0.014, <i>P</i> = 0.015, <i>P</i> = 0.009, and <i>P</i> = 0.014, <i>P</i> = 0.001, <i>P</i> = 0.006, respectively). 30700980 2018
dbSNP: rs2569190
rs2569190
Entrez Id: 929;55374
Gene Symbol: CD14;TMCO6
CD14;TMCO6
CUI: C0041296
Disease:
Tuberculosis
0.010 GeneticVariation BEFREE In the past few years, the relationship between CD14 -159 C>T (rs2569190) polymorphism and risk of TB has been reported in various ethnic populations; however, those studies have yielded contradictory results. 23741383 2013
dbSNP: rs2569190
rs2569190
Entrez Id: 929;55374
Gene Symbol: CD14;TMCO6
CD14;TMCO6
CUI: C1956346
Disease:
Coronary Artery Disease
0.010 GeneticVariation BEFREE In this study, CD14 (rs2569190), CC (P = 0.008) genotypes, and C allele (P = 0.007) were found to be a positive risk factor, while TT genotype (P = 0.045) and T allele (P = 0.007) as negative risk factor for CAD. 29299748 2018
dbSNP: rs2569190
rs2569190
Entrez Id: 929;55374
Gene Symbol: CD14;TMCO6
CD14;TMCO6
CUI: C1827849
Disease:
IgE-mediated allergic asthma
0.010 GeneticVariation BEFREE Individuals carrying the TT genotypes for rs2569190 were significantly associated with an increased risk of atopic asthma compared with those carrying the wild-type homozygous CC genotypes [adjusted odds ratio (OR) by gender and age, from 1.075-2.398, P = 0.025]. 25966203 2015
dbSNP: rs2569190
rs2569190
Entrez Id: 929;55374
Gene Symbol: CD14;TMCO6
CD14;TMCO6
CUI: C0155877
Disease:
Allergic asthma
0.010 GeneticVariation BEFREE Individuals carrying the TT genotypes for rs2569190 were significantly associated with an increased risk of atopic asthma compared with those carrying the wild-type homozygous CC genotypes [adjusted odds ratio (OR) by gender and age, from 1.075-2.398, P = 0.025]. 25966203 2015
dbSNP: rs2569190
rs2569190
Entrez Id: 929;55374
Gene Symbol: CD14;TMCO6
CD14;TMCO6
CUI: C0010346
Disease:
Crohn Disease
0.010 GeneticVariation BEFREE Nineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05). 24776844 2014
dbSNP: rs2569190
rs2569190
Entrez Id: 929;55374
Gene Symbol: CD14;TMCO6
CD14;TMCO6
CUI: C0009324
Disease:
Ulcerative Colitis
0.010 GeneticVariation BEFREE Nineteen functional polymorphisms that alter the NFκB-mediated inflammatory response (TLR2 (rs3804099, rs11938228, rs1816702, rs4696480), TLR4 (rs5030728, rs1554973), TLR9 (rs187084, rs352139), LY96 (MD-2) (rs11465996), CD14 (rs2569190), MAP3K14 (NIK) (rs7222094)), TNF-α signaling (TNFA (TNF-α) (rs361525), TNFRSF1A (TNFR1) (rs4149570), TNFAIP3(A20) (rs6927172)) and other cytokines regulated by NFκB (IL1B (rs4848306), IL1RN (rs4251961), IL6 (rs10499563), IL17A (rs2275913), IFNG (rs2430561)) were associated with response to anti-TNF therapy among patients with CD, UC or both CD and UC (P ⩽ 0.05). 24776844 2014
dbSNP: rs2569190
rs2569190
Entrez Id: 929;55374
Gene Symbol: CD14;TMCO6
CD14;TMCO6
CUI: C0027051
Disease:
Myocardial Infarction
0.010 GeneticVariation BEFREE Numerous published studies have investigated the relationship between the CD14-260C>T (rs2569190) polymorphism and the risk of myocardial infarction (MI). 31183977 2019