Source: LHGDN

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 1401
Gene Symbol: CRP
CRP
CUI: C0021368
Disease: Inflammation
Inflammation
0.600 GeneticVariation LHGDN Genetic polymorphisms and the risk of stroke after cardiac surgery. 16051899

2005

Entrez Id: 3569
Gene Symbol: IL6
IL6
CUI: C0021368
Disease: Inflammation
Inflammation
0.570 GeneticVariation LHGDN In conclusion, although COX-2 -765G>C and IL-6 -174G>C polymorphisms were associated with inflammation, consuming a MD (either supplemented with virgin olive oil or nuts) reduced the concentration of inflammation markers regardless of these polymorphisms. 19056642

2009

Entrez Id: 3553
Gene Symbol: IL1B
IL1B
CUI: C0021368
Disease: Inflammation
Inflammation
0.570 GeneticVariation LHGDN In order to further define the clinical impact of genetic variation in this potent proinflammatory pathway we investigated the joint effects of two single nucleotide polymorphisms in the interleukin-1 beta gene [IL-1B(-511) and IL-1B(+3954)] and a variable number tandem repeat polymorphism in intron 2 of the interleukin 1 receptor antagonist gene (IL-1RN VNTR) on postintervention inflammation and occurrence of restenosis in 183 consecutive patients who underwent successful femoropopliteal PTA. 12958619

2003

Entrez Id: 5743
Gene Symbol: PTGS2
PTGS2
CUI: C0021368
Disease: Inflammation
Inflammation
0.570 GeneticVariation LHGDN In conclusion, although COX-2 -765G>C and IL-6 -174G>C polymorphisms were associated with inflammation, consuming a MD (either supplemented with virgin olive oil or nuts) reduced the concentration of inflammation markers regardless of these polymorphisms. 19056642

2009

Entrez Id: 3569
Gene Symbol: IL6
IL6
CUI: C0021368
Disease: Inflammation
Inflammation
0.570 GeneticVariation LHGDN We demonstrate that common genetic variants of CRP (3'UTR 1846C/T) and IL-6 (-174G/C) are significantly associated with the risk of stroke after cardiac surgery, suggesting a pivotal role of inflammation in post-cardiac surgery stroke. 16051899

2005

Entrez Id: 4282
Gene Symbol: MIF
MIF
CUI: C0021368
Disease: Inflammation
Inflammation
0.560 GeneticVariation LHGDN Functional promoter polymorphisms of the macrophage migration inhibitory factor gene in gastric carcinogenesis. 18097599

2008

Entrez Id: 4282
Gene Symbol: MIF
MIF
CUI: C0021368
Disease: Inflammation
Inflammation
0.560 GeneticVariation LHGDN Functional polymorphisms in the promoter region of macrophage migration inhibitory factor and chronic gastritis. 17786285

2007

Entrez Id: 6347
Gene Symbol: CCL2
CCL2
CUI: C0021368
Disease: Inflammation
Inflammation
0.540 GeneticVariation LHGDN Inheritance of the -2518 MCP-1 G allele, which appears to affect hepatic MCP-1 expression, may predispose HCV patients to more severe hepatic inflammation and fibrosis. 14517792

2003

Entrez Id: 3557
Gene Symbol: IL1RN
IL1RN
CUI: C0021368
Disease: Inflammation
Inflammation
0.520 GeneticVariation LHGDN Interleukin-1 receptor antagonist haplotype associated with prostate cancer risk. 16106254

2005

Entrez Id: 3557
Gene Symbol: IL1RN
IL1RN
CUI: C0021368
Disease: Inflammation
Inflammation
0.520 GeneticVariation LHGDN In order to further define the clinical impact of genetic variation in this potent proinflammatory pathway we investigated the joint effects of two single nucleotide polymorphisms in the interleukin-1 beta gene [IL-1B(-511) and IL-1B(+3954)] and a variable number tandem repeat polymorphism in intron 2 of the interleukin 1 receptor antagonist gene (IL-1RN VNTR) on postintervention inflammation and occurrence of restenosis in 183 consecutive patients who underwent successful femoropopliteal PTA. 12958619

2003

Entrez Id: 7040
Gene Symbol: TGFB1
TGFB1
CUI: C0021368
Disease: Inflammation
Inflammation
0.380 GeneticVariation LHGDN Is low-frequency distribution of TGF-beta genotype associated with increased risk for end-stage renal disease? 17417945

2007

Entrez Id: 4843
Gene Symbol: NOS2
NOS2
CUI: C0021368
Disease: Inflammation
Inflammation
0.310 GeneticVariation LHGDN Inducible nitric oxide synthase, nitrotyrosine and p53 mutations in the molecular pathogenesis of Barrett's esophagus and esophageal adenocarcinoma. 17849424

2008

Entrez Id: 6352
Gene Symbol: CCL5
CCL5
CUI: C0021368
Disease: Inflammation
Inflammation
0.220 GeneticVariation LHGDN Hepatitis C virus-seropositive whites with the RANTES -403-A allele were less likely to have severe hepatic inflammation compared with those without (odds ratio, 0.34; P = 0.03). 12557141

2003

Entrez Id: 4314
Gene Symbol: MMP3
MMP3
CUI: C0021368
Disease: Inflammation
Inflammation
0.030 GeneticVariation LHGDN In conclusion, the common MMP-3 5A/6A promoter polymorphism appears to be functional only during specific environmental conditions involving inflammation. 16904077

2006

Entrez Id: 7157
Gene Symbol: TP53
TP53
CUI: C0021368
Disease: Inflammation
Inflammation
0.020 GeneticVariation LHGDN These results indicate that mutations and consequent dysfunction of P53 gene may result in chronic inflammation and hyperplasia in RA patients. 17977211

2005

Entrez Id: 4153
Gene Symbol: MBL2
MBL2
CUI: C0021368
Disease: Inflammation
Inflammation
0.020 GeneticVariation LHGDN Mannose-binding lectin MBL2 gene polymorphisms and outcome of hepatitis C virus-infected patients. 18592362

2008

Entrez Id: 7157
Gene Symbol: TP53
TP53
CUI: C0021368
Disease: Inflammation
Inflammation
0.020 GeneticVariation LHGDN The highly significant association between NTS, reflecting chronic NO-induced cellular protein damage, and endogenous p53 mutations at CpG dinucleotides, provides further evidence for a molecular link between chronic inflammation and esophageal malignancy. 17849424

2008

Entrez Id: 103
Gene Symbol: ADAR
ADAR
CUI: C0021368
Disease: Inflammation
Inflammation
0.010 GeneticVariation LHGDN Since the ADAR1 variants are differentially regulated during acute inflammation, it suggests that the localization of these variants and of A-to-I RNA editing in the cytoplasm, nucleus, and nucleolus is intracellularly reorganized in response to inflammatory stimulation. 12954622

2003

Entrez Id: 51284
Gene Symbol: TLR7
TLR7
CUI: C0021368
Disease: Inflammation
Inflammation
0.010 GeneticVariation LHGDN We analyzed the effect of TLR7 SNPs on grade of inflammation and stage of fibrosis as determined by liver biopsy. 17512627

2007

Entrez Id: 1238
Gene Symbol: ACKR2
ACKR2
CUI: C0021368
Disease: Inflammation
Inflammation
0.010 GeneticVariation LHGDN Genetic variations of the chemokine scavenger receptor D6 are associated with liver inflammation in chronic hepatitis C. 18822328

2008

Entrez Id: 5354
Gene Symbol: PLP1
PLP1
CUI: C0021368
Disease: Inflammation
Inflammation
0.010 GeneticVariation LHGDN This case raises questions about the role of inflammation in PLP1-related disorders and, conversely, PLP1 mutations in MS. 17438221

2007

Entrez Id: 2957
Gene Symbol: GTF2A1
GTF2A1
CUI: C0021368
Disease: Inflammation
Inflammation
0.010 GeneticVariation LHGDN Human genome search in celiac disease: mutated gliadin T-cell-like epitope in two human proteins promotes T-cell activation. 12054857

2002

Entrez Id: 1401
Gene Symbol: CRP
CRP
CUI: C0021368
Disease: Inflammation
Inflammation
0.600 Biomarker LHGDN The acute-phase reactant C-reactive protein (CRP) has been shown to reflect systemic and, perhaps, vascular inflammation and to predict future cardiovascular events in asymptomatic individuals. 12213988

2001

Entrez Id: 1401
Gene Symbol: CRP
CRP
CUI: C0021368
Disease: Inflammation
Inflammation
0.600 Biomarker LHGDN High-sensitivity C-reactive protein is independently associated with early carotid artery progression in women but not in men: the INVADE Study. 17885262

2007

Entrez Id: 7124
Gene Symbol: TNF
TNF
CUI: C0021368
Disease: Inflammation
Inflammation
0.600 Biomarker LHGDN These results are in agreement with the hypothesis that the synthesis of adipose tissue TNFalpha and leptin could induce the production of interleukin-6, CRP, and other acute-phase reactants, thus contributing to the maintenance of chronic low-grade inflammation state involved in the progression of obesity and its associated comorbidities. 12690081

2003