Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Hypertension, Diastolic, Resistance to
0.300 Biomarker disease CTD_human
CUI: C1840375
Disease: Elevated diastolic blood pressure
Elevated diastolic blood pressure
0.100 Biomarker phenotype HPO
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.550 Biomarker group CTD_human KCNMB1 is involved in calcium sensitivity and hypertension. 17700361 2007
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.550 Biomarker group BEFREE KCNMB1 is involved in calcium sensitivity and hypertension. 17700361 2007
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.550 GeneticVariation group BEFREE KCNMB1 gain-of-function variant Glu65Lys results in generalized vasorelaxation and thus protection against systemic hypertension. 20861615 2010
CUI: C0235222
Disease: Diastolic hypertension
Diastolic hypertension
0.040 GeneticVariation disease BEFREE A recent study reported a new polymorphism (E65 K) in the beta(1) subunit (KCNMB1) gene of the Ca(2+)-dependent potassium channel with a protective effect against the severity of diastolic hypertension, but further data have lead to conflicting results. 16155733 2005
CUI: C0152171
Disease: Idiopathic pulmonary hypertension
Idiopathic pulmonary hypertension
0.010 AlteredExpression disease BEFREE Additionally, overexpression of miR-29b in normal PASMC decreased large-conductance Ca<sup>2+</sup>-activated K<sup>+</sup> (BK<sub>Ca</sub>) channel currents and downregulated BK<sub>Ca</sub> channel β1 subunit (BK<sub>Ca</sub>β1 or KCNMB1) expression, while inhibition of miR-29b in IPAH-PASMC increased BK<sub>Ca</sub> channel activity and BK<sub>Ca</sub>β1 levels. 31553627 2020
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.550 Biomarker group RGD Altered expression of BK channel beta1 subunit in vascular tissues from spontaneously hypertensive rats. 16814121 2006
CUI: C0001883
Disease: Airway Obstruction
Airway Obstruction
0.010 GeneticVariation group LHGDN An african-specific functional polymorphism in KCNMB1 shows sex-specific association with asthma severity. 18535015 2008
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.550 Biomarker group BEFREE Association analysis between hypertension and CYBA, CLCNKB, and KCNMB1 functional polymorphisms in the Japanese population--the Suita Study. 15671602 2005
CUI: C0035078
Disease: Kidney Failure
Kidney Failure
0.010 GeneticVariation disease 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
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
CUI: C0017638
Disease: Glioma
Glioma
0.010 AlteredExpression disease LHGDN Current transients associated with BK channels in human glioma cells. 12962281 2003
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: 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: 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: 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: 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
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
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
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
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: 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