SCAP, SREBF chaperone, 22937

N. diseases: 35; N. variants: 3
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C2712907
Disease: obsolete Combined hyperlipidemia
obsolete Combined hyperlipidemia
0.010 GeneticVariation disease BEFREE We also report additional common single-nucleotide polymorphisms in the SCAP promoter and coding sequence that were identified by using direct sequencing to screen the genomic DNA of subjects with combined hyperlipidemia. 12202990 2002
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
0.310 Biomarker disease CTD_human Dietary alpha-linolenic acid reduces COX-2 expression and induces apoptosis of hepatoma cells. 14563831 2004
CUI: C0003850
Disease: Arteriosclerosis
Arteriosclerosis
0.030 Biomarker disease BEFREE Both SREBP-2 and SCAP are candidates to contribute to the development of atherosclerosis. 16466730 2006
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis
0.030 Biomarker disease BEFREE Both SREBP-2 and SCAP are candidates to contribute to the development of atherosclerosis. 16466730 2006
CUI: C0020443
Disease: Hypercholesterolemia
Hypercholesterolemia
0.200 Biomarker disease RGD Modified HMG-CoA reductase and LDLr regulation is deeply involved in age-related hypercholesterolemia. 16741953 2006
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.010 GeneticVariation disease LHGDN SREBP-2 and SCAP isoforms and risk of early onset myocardial infarction. 17383658 2008
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.010 GeneticVariation disease BEFREE SREBP-2 and SCAP isoforms and risk of early onset myocardial infarction. 17383658 2008
CUI: C1561643
Disease: Chronic Kidney Diseases
Chronic Kidney Diseases
0.010 GeneticVariation group BEFREE The Chi-square test, multivariable logistic regression analysis with adjustment for covariates, as well as a stepwise forward selection procedure revealed that ten different polymorphisms were associated (P<0.05) with the prevalence of CKD in high- or low-risk subjects: the -519Aright curved arrow G polymorphism of MMP1, the 1061Aright curved arrow G (Ile405Val) polymorphism of CETP, the Aright curved arrow G (Lys45Glu) polymorphism of MMP3, the -219Gright curved arrow T polymorphism of APOE, the Aright curved arrow G (Ile1205Val) polymorphism of COL3A1, the -863Cright curved arrow A polymorphism of TNF, and the 1454Cright curved arrow G (Leu125Val) polymorphism of PECAM1 in high-risk subjects; and the 1167Cright curved arrow T (Asn389Asn) polymorphism of TGFBR2, the 2386Aright curved arrow G (Ile796Val) polymorphism of SCAP, and the TAAAright curved arrow del polymorphism of PDE4D in low-risk subjects. 19424605 2009
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.010 GeneticVariation disease BEFREE We conducted a case-control study to investigate whether the common variants of genes from the SREBP2 activating-related pathway, involving SREBP2, SCAP, INSIG1 and INSIG2 genes, were associated with coronary heart disease (CHD) of Chinese Han population individually or interactively. 19740467 2010
CUI: C0011853
Disease: Diabetes Mellitus, Experimental
Diabetes Mellitus, Experimental
0.200 Biomarker disease RGD Differential gene expression pattern of diabetic rat retinas after intravitreal injection of erythropoietin. 20973890 2011
CUI: C0162309
Disease: Adrenoleukodystrophy
Adrenoleukodystrophy
0.010 Biomarker disease BEFREE We used fish which harbor a mutation in the gene encoding the membrane bound transcription factor protease 1 (mbtps1; also called site-1 protease) and embryos in which the Srebp cleavage activating protein (scap) is knocked down to determine the requirement of this pathway in acute ALD. 21284674 2011
CUI: C0010823
Disease: Cytomegalovirus Infections
Cytomegalovirus Infections
0.010 AlteredExpression group BEFREE Our data demonstrate that the induction of PERK during HCMV infection is necessary for full activation of lipogenesis; this effect appears to be mediated by limiting the levels of Insig1 thus freeing SREBP1-SCAP complexes for SREBP1 processing. 23592989 2013
CUI: C0021831
Disease: Intestinal Diseases
Intestinal Diseases
0.010 Biomarker group BEFREE After 4 days of tamoxifen, Vil-Scap(-) mice succumb with a severe enteropathy and near-complete collapse of intestinal mucosa. 25896350 2015
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.020 Biomarker group BEFREE Targeting SCAP N-glycosylation may provide a promising means of treating malignancies and metabolic diseases. 26555173 2015
CUI: C0017636
Disease: Glioblastoma
Glioblastoma
0.020 Biomarker disease BEFREE Xenograft studies reveal that blocking SCAP N-glycosylation ameliorates EGFRvIII-driven glioblastoma growth. 26555173 2015
CUI: C0025517
Disease: Metabolic Diseases
Metabolic Diseases
0.020 Biomarker group BEFREE Targeting SCAP N-glycosylation may provide a promising means of treating malignancies and metabolic diseases. 26555173 2015
CUI: C1621958
Disease: Glioblastoma Multiforme
Glioblastoma Multiforme
0.020 Biomarker disease BEFREE Xenograft studies reveal that blocking SCAP N-glycosylation ameliorates EGFRvIII-driven glioblastoma growth. 26555173 2015
CUI: C0278878
Disease: Adult Glioblastoma
Adult Glioblastoma
0.010 Biomarker disease BEFREE Xenograft studies reveal that blocking SCAP N-glycosylation ameliorates EGFRvIII-driven glioblastoma growth. 26555173 2015
CUI: C0280474
Disease: Childhood Glioblastoma
Childhood Glioblastoma
0.010 Biomarker disease BEFREE Xenograft studies reveal that blocking SCAP N-glycosylation ameliorates EGFRvIII-driven glioblastoma growth. 26555173 2015
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.020 Biomarker disease BEFREE We explored the association between the variants of the sterol-regulatory element-binding transcription factor-1 (SREBF1) gene and the SREBP cleavage-activation protein (SCAP) gene with AAP-induced MetS in a genetic case-control study. 26982812 2016
CUI: C0017636
Disease: Glioblastoma
Glioblastoma
0.020 Biomarker disease BEFREE Our study reveals a previously unrecognized negative feedback loop in SCAP/SREBP-1 signaling mediated by miR-29 and suggests that miR-29 treatment may represent an effective means to target GBM. 27477273 2016
CUI: C1621958
Disease: Glioblastoma Multiforme
Glioblastoma Multiforme
0.020 Biomarker disease BEFREE Our study reveals a previously unrecognized negative feedback loop in SCAP/SREBP-1 signaling mediated by miR-29 and suggests that miR-29 treatment may represent an effective means to target GBM. 27477273 2016
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.020 GeneticVariation disease BEFREE Effect of an SNP in SCAP gene on lipid-lowering response to rosuvastatin in Indian patients with metabolic syndrome. 27885915 2016
CUI: C0011407
Disease: Dental Pulp Necrosis
Dental Pulp Necrosis
0.010 Biomarker disease BEFREE Apical papilla represents a source of an enriched mesenchymal stem cell (MSC) population (stem cells of the apical papilla [SCAPs]) that modulates root development and may participate in regenerative endodontic procedures in immature teeth with pulp necrosis. 28190588 2017
CUI: C0003850
Disease: Arteriosclerosis
Arteriosclerosis
0.030 Biomarker disease BEFREE Effect of Tetramethylpyrazine on Atherosclerosis and SCAP/SREBP-1c Signaling Pathway in ApoE<sup>-/-</sup> Mice Fed with a High-Fat Diet. 28491104 2017