EDN2, endothelin 2, 1907

N. diseases: 32; N. variants: 1
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.200 Biomarker disease RGD Myocardial expression of endothelin-2 is altered reciprocally to that of endothelin-1 during ischemia of cardiomyocytes in vitro and during heart failure in vivo. 10573185 1999
CUI: C0035126
Disease: Reperfusion Injury
Reperfusion Injury
0.200 Biomarker disease RGD The influence of endothelin on vascular and myocardial reperfusion damage was studied with exogenous endothelin-2. 1479622 1992
CUI: C0004096
Disease: Asthma
Asthma
0.010 Biomarker disease BEFREE Tobacco smoking aggravates airway inflammation by upregulating endothelin-2 and activating the c-Jun amino terminal kinase pathway in asthma. 31629215 2019
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation
0.010 GeneticVariation disease BEFREE The EDN2 A985 allele, which is considered to be protective in cardiovascular disease, may be a risk factor for AF in patients with HCM. 18037749 2007
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation
0.010 GeneticVariation disease LHGDN The EDN2 A985 allele, which is considered to be protective in cardiovascular disease, may be a risk factor for AF in patients with HCM. 18037749 2007
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon
0.010 PosttranslationalModification disease BEFREE Mechanistic studies revealed hypermethylation of EDN2 and EDN3 genes in human primary colon cancers and in a panel of human colon cancer cell lines. 22865632 2013
CUI: C0007134
Disease: Renal Cell Carcinoma
Renal Cell Carcinoma
0.010 Biomarker disease BEFREE Cloning and sequencing of a human endothelin converting enzyme in renal adenocarcinoma (ACHN) cells producing endothelin-2. 7695628 1995
CUI: C0007194
Disease: Hypertrophic Cardiomyopathy
Hypertrophic Cardiomyopathy
0.010 GeneticVariation disease LHGDN A985G polymorphism of the endothelin-2 gene and atrial fibrillation in patients with hypertrophic cardiomyopathy. 18037749 2007
CUI: C0007194
Disease: Hypertrophic Cardiomyopathy
Hypertrophic Cardiomyopathy
0.010 GeneticVariation disease BEFREE The EDN2 A985 allele, which is considered to be protective in cardiovascular disease, may be a risk factor for AF in patients with HCM. 18037749 2007
CUI: C0008497
Disease: Choriocarcinoma
Choriocarcinoma
0.010 AlteredExpression disease BEFREE Endothelin-2 down-regulation occurs in parallel with the anti-proliferative effect of dimethylsulfoxide in BeWO human choriocarcinoma cell line. 15619356 2004
CUI: C0013537
Disease: Eclampsia
Eclampsia
0.010 GeneticVariation disease BEFREE The polymorphisms of eNOS G894T and ET-2 A985G genes are correlated with the occurrence of eclampsia. 31486478 2019
CUI: C0017601
Disease: Glaucoma
Glaucoma
0.010 Biomarker disease BEFREE Since endothelin 2 is potently vasoconstrictive and was produced by microglia/macrophages, our data provide what we believe to be a novel link between these cell types and vascular dysfunction in glaucoma. 21383504 2011
CUI: C0032460
Disease: Polycystic Ovary Syndrome
Polycystic Ovary Syndrome
0.010 AlteredExpression disease BEFREE In GLCs from women with PCOS, Endothelin-1 mRNA expression was elevated (2.2-fold) as compared with normally ovulating women, whereas endothelin-2 mRNA was reduced (1.8-fold). 22727793 2012
CUI: C0035372
Disease: Rett Syndrome
Rett Syndrome
0.010 Biomarker disease BEFREE The expression levels of exocytosis-related genes (Stx5a, Syt6), genes encoding secretory (Fgf2, Fgf4, Edn2) and synaptic proteins (Grin2b, Gabbr1), neurotrophin signaling-associated genes (Sos1, Shc1, Traf6, Psen2), and a gene for Rett syndrome (Mecp2) were significantly changed. 28041965 2017
CUI: C0085580
Disease: Essential Hypertension
Essential Hypertension
0.010 Biomarker disease BEFREE Recent work has incriminated endothelin-2 (ET2) as a candidate gene for human essential hypertension. 10489105 1999
CUI: C0699790
Disease: Colon Carcinoma
Colon Carcinoma
0.010 PosttranslationalModification disease BEFREE Epigenetic inactivation of endothelin-2 and endothelin-3 in colon cancer. 22865632 2013
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke
0.010 Biomarker disease BEFREE Our study aims to find out whether mRNA expressions and plasma concentrations of endothelin-1 (ET-l), endothelin-2 (ET-2) and endothelin-3 (ET-3) remain different in IS sufferers with low HcT and Hb levels in comparison with those whose HcT i Hb levels during a severe IS episode remain within the norm. 30047329 2018
CUI: C1998028
Disease: Photoreceptor degeneration
Photoreceptor degeneration
0.010 GeneticVariation disease BEFREE Endothelin-2-mediated protection of mutant photoreceptors in inherited photoreceptor degeneration. 23469133 2013
Hypertrophic obstructive cardiomyopathy
0.010 GeneticVariation disease BEFREE A985G polymorphism of the endothelin-2 gene and atrial fibrillation in patients with hypertrophic cardiomyopathy. 18037749 2007
CUI: C0020649
Disease: Hypotension
Hypotension
0.300 Therapeutic phenotype CTD_human Evidence for antagonistic activity of endothelin for clonidine induced hypotension and bradycardia. 1309933 1992
CUI: C0428977
Disease: Bradycardia
Bradycardia
0.300 Therapeutic phenotype CTD_human Evidence for antagonistic activity of endothelin for clonidine induced hypotension and bradycardia. 1309933 1992
Low density lipoprotein cholesterol measurement
0.100 GeneticVariation phenotype GWASDB Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. 23063622 2012
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.100 GeneticVariation phenotype GWASDB Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. 23063622 2012
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement
0.100 GeneticVariation phenotype GWASDB Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. 23063622 2012
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.100 GeneticVariation phenotype GWASDB Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. 23063622 2012