BRAP, BRCA1 associated protein, 8315

N. diseases: 82; N. variants: 10
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0013124
Disease: Drinking behavior processes
Drinking behavior processes
0.100 GeneticVariation disease GWASDB Common variants at 12q24 are associated with drinking behavior in Han Chinese. 23364009 2013
CUI: C0003962
Disease: Ascites
Ascites
0.010 Biomarker phenotype BEFREE Complete Genome Sequence of <i>bla</i><sub>IMP-6</sub>-Positive <i>Metakosakonia</i> sp. MRY16-398 Isolate From the Ascites of a Diverticulitis Patient. 30524415 2018
CUI: C0013124
Disease: Drinking behavior processes
Drinking behavior processes
0.100 GeneticVariation disease GWASDB Confirmation of ALDH2 as a Major locus of drinking behavior and of its variants regulating multiple metabolic phenotypes in a Japanese population. 21372407 2011
CUI: C0752347
Disease: Lewy Body Disease
Lewy Body Disease
0.030 Biomarker disease BEFREE Diagnosis of dementia with Lewy bodies: can <sup>123</sup>I-IMP and <sup>123</sup>I-MIBG scintigraphy yield new core features? 27897064 2017
CUI: C0028754
Disease: Obesity
Obesity
0.010 GeneticVariation disease BEFREE Effect of dietary energy and polymorphisms in BRAP and GHRL on obesity and metabolic traits. 27245511 2019
CUI: C0017926
Disease: Glycogen Storage Disease Type VII
Glycogen Storage Disease Type VII
0.010 AlteredExpression disease BEFREE Exposure to a calmodulin antagonist significantly slows IMP accumulation during experimental energy imbalance in patients' cells to levels that are similar to those in untreated controls, implying that Ca2+-calmodulin is involved in erythrocyte AMP deaminase activation in familial phosphofructokinase deficiency. 16670071 2006
CUI: C0546837
Disease: Malignant neoplasm of esophagus
Malignant neoplasm of esophagus
0.100 GeneticVariation disease GWASDB Genome-wide association study identifies three new susceptibility loci for esophageal squamous-cell carcinoma in Chinese populations. 21642993 2011
CUI: C0001973
Disease: Alcoholic Intoxication, Chronic
Alcoholic Intoxication, Chronic
0.120 GeneticVariation disease GWASCAT Genome-wide association study of alcohol dependence in male Han Chinese and cross-ethnic polygenic risk score comparison. 31591379 2019
CUI: C0236664
Disease: Alcohol-Related Disorders
Alcohol-Related Disorders
0.100 GeneticVariation group GWASCAT Genome-wide association study of alcohol dependence in male Han Chinese and cross-ethnic polygenic risk score comparison. 31591379 2019
CUI: C0236970
Disease: Alcohol-Induced Disorders
Alcohol-Induced Disorders
0.100 GeneticVariation group GWASCAT Genome-wide association study of alcohol dependence in male Han Chinese and cross-ethnic polygenic risk score comparison. 31591379 2019
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.120 GeneticVariation disease GWASDB Genome-wide association study of coronary artery disease in the Japanese. 21971053 2012
Alanine aminotransferase measurement
0.100 GeneticVariation phenotype GWASCAT Genome-wide association study of hematological and biochemical traits in a Japanese population. 20139978 2010
Serum Alanine Aminotransferase Measurement
0.100 GeneticVariation phenotype GWASCAT Genome-wide association study of hematological and biochemical traits in a Japanese population. 20139978 2010
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption
0.100 GeneticVariation phenotype GWASDB Genome-wide testing of putative functional exonic variants in relationship with breast and prostate cancer risk in a multiethnic population. 23555315 2013
CUI: C0202239
Disease: Uric acid measurement (procedure)
Uric acid measurement (procedure)
0.100 GeneticVariation phenotype GWASCAT Identification of CDC42BPG as a novel susceptibility locus for hyperuricemia in a Japanese population. 29124443 2018
CUI: C0523631
Disease: Folic acid measurement
Folic acid measurement
0.100 GeneticVariation phenotype GWASCAT Identification of three novel loci of ALDH2 Gene for Serum Folate levels in a Male Chinese Population by Genome-Wide Association Study. 29953918 2018
CUI: C0017638
Disease: Glioma
Glioma
0.030 AlteredExpression disease BEFREE Immuno-PET quantitation of de2-7 epidermal growth factor receptor expression in glioma using 124I-IMP-R4-labeled antibody ch806. 20484439 2010
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon
0.010 Biomarker disease BEFREE In colon CA IAI isolates susceptibilities did not reach 80% for AMK and ETP, and in pancreatic IAIs susceptibilities of HA GNBs did not reach 80% to AMK, TZP and ETP, and CA GNBs to IMP and ETP. 30453893 2018
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.040 GeneticVariation disease BEFREE In addition, a combined analysis of BRAP and another CAD locus on 9p21 suggested that these loci had a synergistic role in the susceptibility. 19713974 2009
CUI: C1112209
Disease: Abdominal Infection
Abdominal Infection
0.010 AlteredExpression group BEFREE In colon CA IAI isolates susceptibilities did not reach 80% for AMK and ETP, and in pancreatic IAIs susceptibilities of HA GNBs did not reach 80% to AMK, TZP and ETP, and CA GNBs to IMP and ETP. 30453893 2018
CUI: C1269955
Disease: Tumor Cell Invasion
Tumor Cell Invasion
0.010 Biomarker phenotype BEFREE In parallel, we found that BRAP knockdown increased tumour growth and invasion and decreased survival in an in vivo glioma xenograft mouse model. 31776938 2020
Squamous cell carcinoma of esophagus
0.010 AlteredExpression disease BEFREE In patient tumors, 90% of ESCCs examined had higher levels of BRAP protein than paired non-tumor tissues, and 63.8% had gains in BRAP DNA copy number. 28780075 2017
CUI: C0752347
Disease: Lewy Body Disease
Lewy Body Disease
0.030 Biomarker disease BEFREE In the dementia groups, receiver operating characteristic analysis of the CIS ratio showed significant accuracy for differentiating between AD and DLB on both FDG PET and IMP SPECT. 30075285 2018
CUI: C0001973
Disease: Alcoholic Intoxication, Chronic
Alcoholic Intoxication, Chronic
0.120 GeneticVariation disease BEFREE In the present case-control analysis, <i>BRAP rs3782886</i> showed the most significant association signal with a risk of AD (<i>P</i>=1.29×10<sup>-16</sup>, <i>P<sub>corr</sub></i> =7.74×10<sup>-16</sup>, OR =0.19). 30636874 2019
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.040 Biomarker disease BEFREE In the replication phase, involving 3052 cases and 6335 controls, 12 SNPs were tested; CAD association was replicated and/or verified for 4 (of 12) SNPs from 3 loci: near BRAP and ALDH2 on 12q24 (P=1.6 × 10(-34)), HLA-DQB1 on 6p21 (P=4.7 × 10(-7)), and CDKN2A/B on 9p21 (P=6.1 × 10(-16)). 21971053 2012