Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0011853
Disease: Diabetes Mellitus, Experimental
Diabetes Mellitus, Experimental
0.200 Biomarker disease RGD [Ca(2+)-activated K(+) channel switching in smooth muscle participates in atherosclerosis development in diabetic rats]. 24589593 2014
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.550 GeneticVariation group BEFREE We also found that the carriers of minor T allele of KCNMB1-rs11739136 had a significantly decreased risk for hypertension (TT+CT vs. CC; odds ratio=0.83; 95% confidence interval, 0.72-0.95; P value after the Bonferroni correction=0.008 x 5=0.040). 18496125 2008
CUI: C0003850
Disease: Arteriosclerosis
Arteriosclerosis
0.010 Biomarker disease BEFREE To determine the relationship between atherosclerosis and KCNMB1, we studied some atherogenic factors affecting vascular tone. 25576871 2015
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis
0.010 Biomarker disease BEFREE To determine the relationship between atherosclerosis and KCNMB1, we studied some atherogenic factors affecting vascular tone. 25576871 2015
CUI: C0004610
Disease: Bacteremia
Bacteremia
0.010 Biomarker disease BEFREE These results demonstrate that GAS infection preferentially induces ineffective LAP to evade xenophagic killing in endothelial cells through the SLO/β1 integrin/NOX2/ROS pathway.<b>IMPORTANCE</b> Our previous reports showed that the LC3-associated GAS-containing single membrane vacuoles are inefficient for bacterial clearance in endothelial cells, which may result in bacteremia. 31575768 2019
CUI: C0034069
Disease: Pulmonary Fibrosis
Pulmonary Fibrosis
0.010 Biomarker disease BEFREE The Role of KCNMB1 and BK Channels in Myofibroblast Differentiation and Pulmonary Fibrosis. 31486669 2020
CUI: C0085580
Disease: Essential Hypertension
Essential Hypertension
0.020 GeneticVariation disease BEFREE The dominant model of KCNJ11 E23K and KCNMB1 E65K might be susceptible factors for essential hypertension. 31169684 2019
CUI: C0004096
Disease: Asthma
Asthma
0.010 GeneticVariation disease LHGDN The C818T SNP and four other KCNMB1 variants were genotyped in two independent groups of African American asthmatics (n = 509) and tested for association with the pulmonary function measure--forced expiratory volume (FEV(1)) % of predicted value. 18535015 2008
CUI: C0004096
Disease: Asthma
Asthma
0.010 GeneticVariation disease BEFREE The C818T SNP and four other KCNMB1 variants were genotyped in two independent groups of African American asthmatics (n = 509) and tested for association with the pulmonary function measure--forced expiratory volume (FEV(1)) % of predicted value. 18535015 2008
CUI: C0235222
Disease: Diastolic hypertension
Diastolic hypertension
0.040 GeneticVariation disease BEFREE The rs11739136 KCNMB1 Glu65Lys polymorphism in the beta1 subunit of the Ca2+ and voltage-dependent potassium channel has, in some studies, been reported to associate with a protective effect on diastolic hypertension. 18854753 2008
CUI: C0021655
Disease: Insulin Resistance
Insulin Resistance
0.200 Biomarker phenotype RGD Reduction of large-conductance Ca²(+) -activated K(+) channel with compensatory increase of nitric oxide in insulin resistant rats. 21425425 2011
CUI: C0235222
Disease: Diastolic hypertension
Diastolic hypertension
0.040 GeneticVariation disease BEFREE Protective effect of the KCNMB1 E65K genetic polymorphism against diastolic hypertension in aging women and its relevance to cardiovascular risk. 16293791 2005
CUI: C0003130
Disease: Anoxia
Anoxia
0.010 AlteredExpression phenotype LHGDN Post-transcriptional control of human maxiK potassium channel activity and acute oxygen sensitivity by chronic hypoxia. 14522958 2003
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.550 AlteredExpression group LHGDN Maxi-K+ channel beta1 expression in sleep apnea patients and its modulation by CPAP treatment. 19057512 2009
CUI: C0520679
Disease: Sleep Apnea, Obstructive
Sleep Apnea, Obstructive
0.010 Biomarker disease LHGDN Maxi-K+ channel beta1 expression in sleep apnea patients and its modulation by CPAP treatment. 19057512 2009
Ventricular Fibrillation, Paroxysmal Familial, 1
0.010 GeneticVariation disease BEFREE It is suggested that coexpression of hbeta(1) exposes a more severe functional defect that results in a greater overlap in the relationship between channel inactivation and activation (window current) in T1620M, which is proposed to be a potential pathophysiological mechanism of IVF in vivo. 10618304 2000
Diabetes Mellitus, Non-Insulin-Dependent
0.200 Biomarker disease RGD Impaired Ca2+-dependent activation of large-conductance Ca2+-activated K+ channels in the coronary artery smooth muscle cells of Zucker Diabetic Fatty rats. 18790848 2008
CUI: C0043094
Disease: Weight Gain
Weight Gain
0.300 Biomarker phenotype CTD_human High-fat diet-induced obesity alters nitric oxide-mediated neuromuscular transmission and smooth muscle excitability in the mouse distal colon. 27288421 2016
CUI: C0085580
Disease: Essential Hypertension
Essential Hypertension
0.020 GeneticVariation disease BEFREE Genotype and allele frequency analyses revealed that the frequency of genotypes KCNJ11-rs2285676 and KCNMB1-rs11739136 was not significantly different between the EH and NT groups. 28962116 2017
CUI: C0235222
Disease: Diastolic hypertension
Diastolic hypertension
0.040 GeneticVariation disease BEFREE Gain-of-function mutation in the KCNMB1 potassium channel subunit is associated with low prevalence of diastolic hypertension. 15057310 2004
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis
0.010 GeneticVariation disease BEFREE E65 K polymorphism in KCNMB1 gene is not associated with ischaemic heart disease in Spanish patients. 16155733 2005
CUI: C0151744
Disease: Myocardial Ischemia
Myocardial Ischemia
0.010 GeneticVariation disease BEFREE E65 K polymorphism in KCNMB1 gene is not associated with ischaemic heart disease in Spanish patients. 16155733 2005
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.550 Biomarker group RGD Downregulation of the BK channel beta1 subunit in genetic hypertension. 14551242 2003
CUI: C0017638
Disease: Glioma
Glioma
0.010 AlteredExpression disease LHGDN Current transients associated with BK channels in human glioma cells. 12962281 2003
CUI: C1561643
Disease: Chronic Kidney Diseases
Chronic Kidney Diseases
0.010 GeneticVariation group BEFREE Common KCNMB1 gain-of-function variant Glu65Lys influences GFR, and 65Lys carriers exhibit not only elevated baseline GFR, but also more rapid GFR decline (and consequent development of renal failure) in CKD. 20861615 2010