Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis
0.370 GeneticVariation disease BEFREE Studies in mice followed by several extensive clinical studies have identified ALOX5 and ALOX5AP polymorphisms as strong risk factors for atherosclerosis and cerebrovascular pathologies. 16278051 2006
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis
0.370 Biomarker disease BEFREE Arachidonate 5-lipoxygenase activating protein (ALOX5AP) gene is involved in the pathogenesis of atherosclerotic cardiovascular disease (CVD). 16261187 2006
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis
0.370 Biomarker disease CTD_human Expression of 5-lipoxygenase and leukotriene A4 hydrolase in human atherosclerotic lesions correlates with symptoms of plaque instability. 16698924 2006
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis
0.370 Biomarker disease BEFREE Recently, leukotriene-based inflammation has also been shown to play an important role in atherosclerosis: ALOX5AP and LTA4H, both genes in the leukotriene biosynthesis pathway, have individually been shown to be associated with various cardiovascular disease (CVD) phenotypes. 19130089 2009
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis
0.370 GeneticVariation disease BEFREE The 5-lipoxygenase activating protein (FLAP), encoded by the activating 5-lipoxygenase (ALOX5AP) gene, is a crucial mediator of the biosynthesis of leukotrienes, which have been implicated in atherosclerosis. 22726381 2012
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis
0.370 GeneticVariation disease BEFREE This transcriptional activation was associated with the binding of HIF-1 to the FLAP promoter and was strongly associated with atherosclerosis lesion size. 29920371 2018
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis
0.370 Biomarker disease BEFREE Polymorphisms within ALOX12, ALOX5, and ALOX5AP are genetically associated with subclinical atherosclerosis and with biomarkers of disease in families with type 2 diabetes. 20592751 2010
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis
0.370 Biomarker disease BEFREE The eicosanoid genes ALOX5, ALOX5AP and LTA4H have been implicated in atherosclerosis. 25721704 2015
CUI: C0007785
Disease: Cerebral Infarction
Cerebral Infarction
0.370 GeneticVariation disease BEFREE The Chi-square test, multivariable logistic regression analysis with adjustment for age, sex, body mass index, and the prevalence of hypertension, hypercholesterolemia, and diabetes mellitus, as well as a stepwise forward selection procedure revealed that the 2445G-->A (Ala54Thr) polymorphism (rs1799883) of FABP2, the -108/3G-->4G polymorphism of IPF1 (S82168), the A-->G (rs2241883" genes_norm="2168">Thr94Ala) polymorphism (rs2241883) of FABP1, the G-->A (rs529038" genes_norm="6098">Asp2213Asn) polymorphism (rs529038) of ROS1, the -11377C-->G polymorphism (rs266729) of ADIPOQ, the 162A-->C polymorphism (rs4769055) of ALOX5AP, the -786T-->C polymorphism (rs2070744) of NOS3, and the 3279C-->T polymorphism (rs7291467) of LGALS2 were associated (P<0.05) with the prevalence of atherothrombotic cerebral infarction. 18506375 2008
CUI: C0007785
Disease: Cerebral Infarction
Cerebral Infarction
0.370 GeneticVariation disease BEFREE The results of the meta-analysis indicate that ALOX5AP rs10507391/SG13S114 A>T polymorphism is not associated with the risk of cerebral infarction in the Chinese population. 25242267 2015
CUI: C0007785
Disease: Cerebral Infarction
Cerebral Infarction
0.370 Biomarker disease BEFREE However, the interaction between ALOX5AP-SG13S114AA and COX-2-765CC apparently increases susceptibility to cerebral infarction. 23765972 2013
CUI: C0007785
Disease: Cerebral Infarction
Cerebral Infarction
0.370 GeneticVariation disease BEFREE The results indicate that the two genetic polymorphisms of ALOX5AP, SG13S114 and SG13S32, are not associated with cerebral infarction in Chinese Han population. 23546934 2013
CUI: C0007785
Disease: Cerebral Infarction
Cerebral Infarction
0.370 GeneticVariation disease BEFREE Interaction between ALOX5AP and CYP3A5 gene variants significantly increases the risk for cerebral infarctions in Chinese. 24368493 2014
CUI: C0007785
Disease: Cerebral Infarction
Cerebral Infarction
0.370 Biomarker disease CTD_human
CUI: C0007785
Disease: Cerebral Infarction
Cerebral Infarction
0.370 GeneticVariation disease BEFREE Synergistic effect of ALOX5AP polymorphisms and cigarette smoking on the risk of atherosclerotic cerebral infarction in a Northern Han Chinese population. 24411318 2014
CUI: C0007785
Disease: Cerebral Infarction
Cerebral Infarction
0.370 GeneticVariation disease BEFREE Association of ALOX5AP gene single nucleotide polymorphisms and cerebral infarction in the Han population of northern China. 22849376 2012
CUI: C0149504
Disease: Encephalopathy, Toxic
Encephalopathy, Toxic
0.300 Biomarker disease CTD_human Blood gene expression markers to detect and distinguish target organ toxicity. 19784758 2010
CUI: C0154659
Disease: Toxic Encephalitis
Toxic Encephalitis
0.300 Biomarker disease CTD_human Blood gene expression markers to detect and distinguish target organ toxicity. 19784758 2010
CUI: C0751014
Disease: Subcortical Infarction
Subcortical Infarction
0.300 Biomarker disease CTD_human
CUI: C0017658
Disease: Glomerulonephritis
Glomerulonephritis
0.200 ModifyingMutation disease RGD Increased 5-lipoxygenase activating protein in immune-mediated experimental nephritis. 14733414 2004
CUI: C0004096
Disease: Asthma
Asthma
0.100 GeneticVariation disease BEFREE Although the studied polymorphisms have been previously reported to constitute risk factors for the disease, we found no association between LTC4S -444 A/C, ALOX5 -176/-147, and ALOX5AP -169/-146 polymorphisms and bronchial asthma. 20128419 2009
CUI: C0004096
Disease: Asthma
Asthma
0.100 GeneticVariation disease BEFREE No ALOX5AP allele was associated with asthma or asthma-related phenotypes in case-control or TDT analyses. 12911785 2003
CUI: C0004096
Disease: Asthma
Asthma
0.100 GeneticVariation disease BEFREE We confirmed the presence of two polymorphisms in intron 2 and found no association between these polymorphisms and asthma or asthma severity, nor between a promoter polymorphism in the ALOX5AP gene and asthma or asthma severity. 15784112 2005
CUI: C0004096
Disease: Asthma
Asthma
0.100 AlteredExpression disease BEFREE These data suggest that up-regulation of 5-LO and FLAP mRNAs might be involved in the increased leukotriene synthesis and play an important role in the pathogenesis of asthma. 9642160 1998
CUI: C0004096
Disease: Asthma
Asthma
0.100 GeneticVariation disease BEFREE LTA4H and ALOX5AP gene polymorphisms modify the augmentation of bronchodilator responsiveness by leukotriene modifiers in Puerto Ricans but not Mexicans with asthma. 20810156 2010