VNN1, vanin 1, 8876

N. diseases: 40; N. variants: 2
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases
0.310 AlteredExpression group BEFREE VNN1 is expressed by enterocytes and is upregulated in IBD. 23949622 2013
CUI: C0033860
Disease: Psoriasis
Psoriasis
0.310 AlteredExpression disease BEFREE We hypothesize that increased levels of pantetheinase activity are part of the inflammatory-regenerative epidermal differentiation program, and may contribute to the phenotype observed in psoriasis. 19322213 2009
CUI: C0033860
Disease: Psoriasis
Psoriasis
0.310 Biomarker disease CTD_human We hypothesize that increased levels of pantetheinase activity are part of the inflammatory-regenerative epidermal differentiation program, and may contribute to the phenotype observed in psoriasis. 19322213 2009
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases
0.310 Therapeutic group CTD_human Thus, the Vanin-1/pantetheinase activity might be a new target for therapeutic intervention in inflammatory bowel disease. 17145956 2006
CUI: C0007570
Disease: Celiac Disease
Celiac Disease
0.300 Biomarker disease CTD_human Celiac disease biomarkers identified by transcriptome analysis of small intestinal biopsies. 30097691 2018
CUI: C0011615
Disease: Dermatitis, Atopic
Dermatitis, Atopic
0.300 Biomarker disease CTD_human Expression of the vanin gene family in normal and inflamed human skin: induction by proinflammatory cytokines. 19322213 2009
CUI: C0030246
Disease: Pustulosis of Palms and Soles
Pustulosis of Palms and Soles
0.300 Biomarker disease CTD_human Expression of the vanin gene family in normal and inflamed human skin: induction by proinflammatory cytokines. 19322213 2009
CUI: C0086196
Disease: Eczema, Infantile
Eczema, Infantile
0.300 Biomarker disease CTD_human Expression of the vanin gene family in normal and inflamed human skin: induction by proinflammatory cytokines. 19322213 2009
CUI: C0242339
Disease: Dyslipidemias
Dyslipidemias
0.300 Biomarker group CTD_human Discovery of expression QTLs using large-scale transcriptional profiling in human lymphocytes. 17873875 2007
CUI: C0598784
Disease: Dyslipoproteinemias
Dyslipoproteinemias
0.300 Biomarker phenotype CTD_human Discovery of expression QTLs using large-scale transcriptional profiling in human lymphocytes. 17873875 2007
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.030 Biomarker group BEFREE In conclusion, these results suggest that urinary vanin-1 is a potentially sensitive biomarker for ameliorating renal tubular damage in salt-sensitive hypertension. 31514290 2019
CUI: C4324374
Disease: Renal tubular injury
Renal tubular injury
0.030 Biomarker disease BEFREE We have previously demonstrated that urinary vanin-1 is an early biomarker of oxidative renal tubular injury. 31514290 2019
CUI: C4324374
Disease: Renal tubular injury
Renal tubular injury
0.030 Biomarker disease BEFREE Urinary vanin-1 may serve as a candidate biomarker of renal tubular injury due to hydronephrosis. 30332759 2018
CUI: C0009319
Disease: Colitis
Colitis
0.030 Biomarker disease BEFREE Taken together, our studies suggest that GPRC5a is a potential biomarker for colon cancer and promotes tumorigenesis through stimulation of Vanin-1 expression and oxidative stress in colitis associated cancer. 28316092 2017
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.030 AlteredExpression disease BEFREE Elevation of GPRC5A expression in colorectal cancer promotes tumor progression through VNN-1 induced oxidative stress. 28316092 2017
CUI: C4324374
Disease: Renal tubular injury
Renal tubular injury
0.030 Biomarker disease BEFREE Previously, we found a novel renal biomarker, urinary vanin-1, in several animal models with renal tubular injury. 28973979 2017
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.030 Biomarker disease BEFREE A novel transcript, VNN1-AB, as a biomarker for colorectal cancer. 24687856 2014
CUI: C0009319
Disease: Colitis
Colitis
0.030 AlteredExpression disease BEFREE In mouse, we examined Vanin-1 expression in gut and feces during dextran sulfate sodium-induced colitis and assayed the effect of PPARg on Vanin-1 regulation. 23949622 2013
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.030 GeneticVariation group BEFREE We tested the hypothesis that the rs2294757 VNN1 T26I polymorphism could affect blood pressure (BP) levels, hypertension prevalence, and risk of incident cardiovascular events. 21550219 2013
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.030 Biomarker disease BEFREE A 7-gene panel (ANXA3, CLEC4D, LMNB1, PRRG4, TNFAIP6, VNN1 and IL2RB) discriminated CRC in the training set (area under the receiver-operating-characteristic curve (ROC AUC), 0.80; accuracy, 73%; sensitivity, 82%; specificity 64%). 19795455 2010
CUI: C0009319
Disease: Colitis
Colitis
0.030 AlteredExpression disease BEFREE Recent studies in a mouse colitis model indicated that vanin-1 has proinflammatory activity and suggest that pantetheinases are potential therapeutic targets in inflammatory diseases. 19322213 2009
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.030 GeneticVariation group BEFREE Further analyses demonstrated that the missense SNP rs2272996 (or N131S) in the VNN1 gene was significantly associated with hypertension in African Americans and the association was replicated in Mexican Americans; a non-significant opposite association was observed in European Americans. 18043751 2007
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.030 GeneticVariation group LHGDN Further analyses demonstrated that the missense SNP rs2272996 (or N131S) in the VNN1 gene was significantly associated with hypertension in African Americans and the association was replicated in Mexican Americans; a non-significant opposite association was observed in European Americans. 18043751 2007
CUI: C0020295
Disease: Hydronephrosis
Hydronephrosis
0.020 Biomarker disease BEFREE In multivariate analyses, BL vanin-1 and N-acetyl-β-D-glucosaminidase (NAG), but not kidney injury molecule-1 (KIM-1) or neutrophil gelatinase-associated lipocalin (NGAL), were independent factors for predicting the presence of HN. 30791405 2019
CUI: C0178664
Disease: Glomerulosclerosis (disorder)
Glomerulosclerosis (disorder)
0.020 AlteredExpression disease BEFREE Fr-STZ DN rats exhibited obvious tubular renal damage and glomerular podocyte injury as confirmed by renal kidney -injury molecule-1 (KIM-1), neutrophil gelatinase-associated lipocalin (NGAL), and vanin-1 mRNA, as well as urinary N-acetyl-β-D-glucosaminidase elevation and nephrin mRNA suppression, associated with the appearance of marked renal interstitial fibrosis and glomerulosclerosis despite the absence of microalbuminuria. 30699409 2019