VDAC1, voltage dependent anion channel 1, 7416

N. diseases: 116; N. variants: 2
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.300 Biomarker disease CTD_human Long-term oral resveratrol intake provides nutritional preconditioning against myocardial ischemia/reperfusion injury: involvement of VDAC1 downregulation. 25488258 2015
CUI: C0027055
Disease: Myocardial Reperfusion Injury
Myocardial Reperfusion Injury
0.300 Biomarker phenotype CTD_human Long-term oral resveratrol intake provides nutritional preconditioning against myocardial ischemia/reperfusion injury: involvement of VDAC1 downregulation. 25488258 2015
CUI: C0242698
Disease: Ventricular Dysfunction, Left
Ventricular Dysfunction, Left
0.300 Biomarker phenotype CTD_human Long-term oral resveratrol intake provides nutritional preconditioning against myocardial ischemia/reperfusion injury: involvement of VDAC1 downregulation. 25488258 2015
CUI: C0011881
Disease: Diabetic Nephropathy
Diabetic Nephropathy
0.300 Biomarker disease CTD_human Quantitative proteomic profiling identifies new renal targets of copper(II)-selective chelation in the reversal of diabetic nephropathy in rats. 19634143 2009
CUI: C0017667
Disease: Nodular glomerulosclerosis
Nodular glomerulosclerosis
0.300 Biomarker disease CTD_human Quantitative proteomic profiling identifies new renal targets of copper(II)-selective chelation in the reversal of diabetic nephropathy in rats. 19634143 2009
CUI: C0014544
Disease: Epilepsy
Epilepsy
0.300 Biomarker disease CTD_human Preliminary explorations of the role of mitochondrial proteins in refractory epilepsy: some findings from comparative proteomics. 17893921 2007
CUI: C0086237
Disease: Epilepsy, Cryptogenic
Epilepsy, Cryptogenic
0.300 Biomarker disease CTD_human Preliminary explorations of the role of mitochondrial proteins in refractory epilepsy: some findings from comparative proteomics. 17893921 2007
CUI: C0236018
Disease: Aura
Aura
0.300 Biomarker phenotype CTD_human Preliminary explorations of the role of mitochondrial proteins in refractory epilepsy: some findings from comparative proteomics. 17893921 2007
CUI: C0751111
Disease: Awakening Epilepsy
Awakening Epilepsy
0.300 Biomarker disease CTD_human Preliminary explorations of the role of mitochondrial proteins in refractory epilepsy: some findings from comparative proteomics. 17893921 2007
CUI: C0033922
Disease: Psychomotor Disorders
Psychomotor Disorders
0.300 Biomarker group CTD_human Deficiency of the voltage-dependent anion channel: a novel cause of mitochondriopathy. 8726225 1996
CUI: C0162668
Disease: Megaconial Myopathies
Megaconial Myopathies
0.300 Biomarker disease CTD_human Deficiency of the voltage-dependent anion channel: a novel cause of mitochondriopathy. 8726225 1996
CUI: C0162669
Disease: Pleoconial Myopathies
Pleoconial Myopathies
0.300 Biomarker disease CTD_human Deficiency of the voltage-dependent anion channel: a novel cause of mitochondriopathy. 8726225 1996
CUI: C0162670
Disease: Mitochondrial Myopathies
Mitochondrial Myopathies
0.300 Biomarker group CTD_human Deficiency of the voltage-dependent anion channel: a novel cause of mitochondriopathy. 8726225 1996
CUI: C0424230
Disease: Motor retardation
Motor retardation
0.300 Biomarker phenotype CTD_human Deficiency of the voltage-dependent anion channel: a novel cause of mitochondriopathy. 8726225 1996
CUI: C0751456
Disease: Developmental Psychomotor Disorders
Developmental Psychomotor Disorders
0.300 Biomarker group CTD_human Deficiency of the voltage-dependent anion channel: a novel cause of mitochondriopathy. 8726225 1996
CUI: C0949496
Disease: Luft Disease
Luft Disease
0.300 Biomarker disease CTD_human Deficiency of the voltage-dependent anion channel: a novel cause of mitochondriopathy. 8726225 1996
CUI: C0011853
Disease: Diabetes Mellitus, Experimental
Diabetes Mellitus, Experimental
0.200 Biomarker disease RGD Quantitative proteomic profiling identifies new renal targets of copper(II)-selective chelation in the reversal of diabetic nephropathy in rats. 19634143 2009
CUI: C0270824
Disease: Visual seizure
Visual seizure
0.200 Therapeutic disease RGD Preliminary explorations of the role of mitochondrial proteins in refractory epilepsy: some findings from comparative proteomics. 17893921 2007
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.100 Biomarker group BEFREE These data identify the MFF-VDAC1 complex as a novel regulator of mitochondrial cell death and an actionable therapeutic target in cancer. 31582380 2019
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.100 Biomarker group BEFREE The results thus show that VDAC1 depletion-mediated cancer cell metabolic reprograming involves a chain of events occurring in a sequential manner leading to a reversal of the unique properties of the tumor, indicative of the interplay between metabolism and oncogenic signaling networks. 31661894 2019
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.100 AlteredExpression group BEFREE VDAC1 is one of the most studied members of the VDAC protein family and is overexpressed in multiple types of cancer. 31452730 2019
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.100 Biomarker group BEFREE An MFF-VDAC1 complex is a novel regulator of mitochondrial integrity and actionable therapeutic target in cancer. 31542392 2019
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.100 Biomarker group BEFREE As depletion of CCP2 or inhibition of VDAC1 reverses the effects of RARRES1 depletion on energy balance and cell survival we conclude that RARRES1 modulation of CCP2-modulated tubulin-mitochondrial VDAC1 interactions is a fundamental regulator of cancer and stem cell metabolism and survival. 30899431 2019
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.100 Biomarker group BEFREE Although VDAC1 silencing occurred within a day, the cells underwent reprograming with respect to rewiring metabolism, elimination of cancer stem cells (CSCs), and alteration of transcription factor (TF) expression and proteins associated with differentiation, with maximal changes being observed after 3 weeks of silencing VDAC1 expression. 31195298 2019
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.100 AlteredExpression group BEFREE SIGNIFICANCE: These findings describe mitochondrial fission regulation using a peptidomimetic agent that disturbs the MFF-VDAC complex and displays anticancer activity in multiple tumor models.<i>See related commentary by Rao, p. 6074</i>. 31582380 2019