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: C0001973
Disease: Alcoholic Intoxication, Chronic
Alcoholic Intoxication, Chronic
0.120 GeneticVariation disease GWASDB "ALDH2 is associated to alcohol dependence and is the major genetic determinant of ""daily maximum drinks"" in a GWAS study of an isolated rural Chinese sample." 24277619 2014
Conventional (Clear Cell) Renal Cell Carcinoma
0.010 GeneticVariation disease BEFREE <b>Background:</b> Clear cell renal cell carcinoma (ccRCC) is the most prevalent histologic subtype of kidney cancers in adults, which could be divided into two distinct subgroups according to the <i>BRCA1 associated protein-1</i> (<i>BAP1</i>) mutation status. 28900502 2017
CUI: C0740457
Disease: Malignant neoplasm of kidney
Malignant neoplasm of kidney
0.010 GeneticVariation disease BEFREE <b>Background:</b> Clear cell renal cell carcinoma (ccRCC) is the most prevalent histologic subtype of kidney cancers in adults, which could be divided into two distinct subgroups according to the <i>BRCA1 associated protein-1</i> (<i>BAP1</i>) mutation status. 28900502 2017
CUI: C0220633
Disease: Uveal melanoma
Uveal melanoma
0.010 GeneticVariation disease BEFREE Uveal melanoma (UM) remains without effective therapy at the metastatic stage, which is associated with <i>BAP-1</i> (BRCA1 associated protein) mutations. 31146482 2019
CUI: C0035334
Disease: Retinitis Pigmentosa
Retinitis Pigmentosa
0.010 Biomarker disease BEFREE IMP dehydrogenase-linked retinitis pigmentosa. 18600550 2008
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.450 Biomarker disease BEFREE BRCA-1 associated protein (BRAP), a newly identified risk gene for MI, aggravates the inflammatory response in atherosclerosis. 23356535 2013
CUI: C0003850
Disease: Arteriosclerosis
Arteriosclerosis
0.010 Biomarker disease BEFREE BRCA-1 associated protein (BRAP), a newly identified risk gene for MI, aggravates the inflammatory response in atherosclerosis. 23356535 2013
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis
0.010 Biomarker disease BEFREE BRCA-1 associated protein (BRAP), a newly identified risk gene for MI, aggravates the inflammatory response in atherosclerosis. 23356535 2013
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.450 GeneticVariation disease GWASDB A genome-wide association study identifies PLCL2 and AP3D1-DOT1L-SF3A2 as new susceptibility loci for myocardial infarction in Japanese. 24916648 2015
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.450 GeneticVariation disease GWASCAT A genome-wide association study identifies PLCL2 and AP3D1-DOT1L-SF3A2 as new susceptibility loci for myocardial infarction in Japanese. 24916648 2015
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.120 GeneticVariation disease GWASDB A genome-wide association study of a coronary artery disease risk variant. 23364394 2013
CUI: C0019163
Disease: Hepatitis B
Hepatitis B
0.100 GeneticVariation disease GWASDB A genome-wide association study of chronic hepatitis B identified novel risk locus in a Japanese population. 21750111 2011
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.030 Biomarker disease BEFREE A phenomics-based strategy identifies loci on APOC1, BRAP, and PLCG1 associated with metabolic syndrome phenotype domains. 22022282 2011
CUI: C0751007
Disease: Intracranial Atherosclerosis
Intracranial Atherosclerosis
0.010 Biomarker disease BEFREE Acetazolamide reactivity on <sup>123</sup> I-IMP SPECT is used to detect misery perfusion due to intracranial atherosclerosis. 29215168 2018
CUI: C1561643
Disease: Chronic Kidney Diseases
Chronic Kidney Diseases
0.010 GeneticVariation group BEFREE After adjustment for clinical factors, kidney function was associated with BRAP rs3782886 and SPATA5L1 rs2467853 and the GRS for CKD that we developed was associated CKD. 29016630 2017
CUI: C0151773
Disease: Bone marrow depression
Bone marrow depression
0.010 Biomarker disease BEFREE All patients receive folic acid 5 mg daily whilst on the trial IMP to reduce the risk of bone marrow depression. 29402332 2018
CUI: C0424295
Disease: Hyperactive behavior
Hyperactive behavior
0.010 Biomarker phenotype BEFREE Also, administration with SB or IMP could reverse the hyperactivity of hypothalamic-pituitary-adrenal axis as well as decreased inflammatory cytokines with improved antioxidant status. 31353549 2019
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.060 Biomarker group BEFREE Although discussed using variable terminology, cutaneous BRCA1-associated protein (BAP1)-inactivated melanocytic tumor (BIMT) has been considered a discrete diagnostic entity since 2011. 31233225 2019
CUI: C0004610
Disease: Bacteremia
Bacteremia
0.010 Biomarker disease BEFREE Although in-hospital mortality rates were similar between cases and controls (14.3% versus 13.3%), the in-hospital mortality of patients with IMP-producing E. cloacae-caused bacteremia was significantly higher (40%) than the rate in controls. 24709261 2014
CUI: C0017638
Disease: Glioma
Glioma
0.030 Biomarker disease BEFREE Autophagy suppression sensitizes glioma cells to IMP dehydrogenase inhibition-induced apoptotic death. 27818246 2017
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement
0.100 GeneticVariation phenotype GWASCAT Bivariate genome-wide association study identifies novel pleiotropic loci for lipids and inflammation. 27286809 2016
Low density lipoprotein cholesterol measurement
0.100 GeneticVariation phenotype GWASCAT Bivariate genome-wide association study identifies novel pleiotropic loci for lipids and inflammation. 27286809 2016
CUI: C0346153
Disease: Breast Cancer, Familial
Breast Cancer, Familial
0.010 GeneticVariation disease BEFREE BRIP1 is a BRCA1 associated protein that is mutated in a fraction of familial breast cancer and Fanconi anemia cases. 20567916 2010
CUI: C0015625
Disease: Fanconi Anemia
Fanconi Anemia
0.010 GeneticVariation disease BEFREE BRIP1 is a BRCA1 associated protein that is mutated in a fraction of familial breast cancer and Fanconi anemia cases. 20567916 2010
FANCONI ANEMIA, COMPLEMENTATION GROUP A (disorder)
0.010 GeneticVariation disease BEFREE BRIP1 is a BRCA1 associated protein that is mutated in a fraction of familial breast cancer and Fanconi anemia cases. 20567916 2010