BCR, BCR activator of RhoGEF and GTPase, 613

N. diseases: 392; N. variants: 7
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0006840
Disease: Candidiasis
Candidiasis
0.010 Biomarker disease BEFREE Previous studies showed a requirement for <i>Candida</i> biofilm formation on both palate and dentures in infection and identified fungal morphogenic transcription factors, Efg1 and Bcr1, as key players in DS pathogenesis.While both <i>C. albicans</i> and <i>Candida glabrata</i> are frequently coisolated in mucosal candidiasis, a pathogenic role for <i>C. glabrata</i> in DS remains unknown. 30944214 2019
CUI: C0007112
Disease: Adenocarcinoma of prostate
Adenocarcinoma of prostate
0.010 AlteredExpression disease BEFREE <b>Results</b>: High levels of WISP1 correlated with BCR-free survival in prostate adenocarcinoma and overall survival in primary melanoma, low-grade glioma, and kidney papillary cell carcinoma. 31069142 2019
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
Non-Small Cell Lung Carcinoma
0.010 Biomarker disease BEFREE Together, our findings support the antitumor potential of quinoline-chalcone derivatives for NSCLC and CML by inhibiting the PI3K/Akt/mTOR pathway. 30428415 2019
Diabetes Mellitus, Insulin-Dependent
0.010 Biomarker disease BEFREE A Public BCR Present in a Unique Dual-Receptor-Expressing Lymphocyte from Type 1 Diabetes Patients Encodes a Potent T Cell Autoantigen. 31150624 2019
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.010 Biomarker disease BEFREE Our findings strongly suggest PHL as a potent therapeutic agent in treating PD. 31251998 2019
CUI: C0178874
Disease: Tumor Progression
Tumor Progression
0.010 Biomarker phenotype BEFREE This review explores the mechanisms behind cancer progression of these BCR oncogenic fusion proteins, comparing their similarities and differences, examining the significance of BCR as a partner gene, and discussing current treatment options for these translocation-induced hematopoietic malignancies. 31105873 2019
Myelofibrosis due to another disorder
0.010 GeneticVariation disease BEFREE This study aimed to elucidate patterns of disease transformation to secondary myelofibrosis (SMF) or secondary acute myeloid leukemia (SAML) and the development of second primary malignancies in South Korean patients with BCR-ABL1-negative myeloproliferative neoplasms (MPNs). 31765478 2019
CUI: C0271650
Disease: Impaired glucose tolerance
Impaired glucose tolerance
0.010 Biomarker phenotype BEFREE The DIO models took several months to become obese, exhibited less severe hyperglycaemia and glucose intolerance, while glycation products were not significantly different between these groups (with the exception of furosine in liver and CML in lungs). 30467969 2019
CUI: C0278838
Disease: Prostate cancer recurrent
Prostate cancer recurrent
0.010 Biomarker disease BEFREE Five patients with PCa and BCR, following radical prostatectomy, underwent 68Ga-PSMA PET/CT. 30901173 2019
CUI: C0280449
Disease: secondary acute myeloid leukemia
secondary acute myeloid leukemia
0.010 GeneticVariation disease BEFREE This study aimed to elucidate patterns of disease transformation to secondary myelofibrosis (SMF) or secondary acute myeloid leukemia (SAML) and the development of second primary malignancies in South Korean patients with BCR-ABL1-negative myeloproliferative neoplasms (MPNs). 31765478 2019
HODGKIN'S AND NON-HODGKIN'S LYMPHOMA
0.010 GeneticVariation disease BEFREE Our findings showed BMI, and BMI in early adulthood (aged 18-21 years) is associated with the risk of Hodgkin's and non-Hodgkin's lymphoma (HL and NHL), diffuse large beta-cell lymphoma (DLBCL), Leukaemia including acute and chronic myeloid lymphoma (AML and CML), and chronic lymphocytic leukaemia (CLL) and multiple myeloma (MM). 30753270 2019
CUI: C0521585
Disease: Gastrointestinal mucositis
Gastrointestinal mucositis
0.010 GeneticVariation disease BEFREE An 11-year-old male patient with the deletion of <i>IKZF1</i> (Ikaros family zinc finger 1) and positive Breakpoint Cluster Region-C-Abelson oncogene 1(<i>BCR-ABL1</i>) acute lymphoblastic leukemia developed mucositis, gastrointestinal toxicity, hepatotoxicity, myelosuppression, and severe dermatologic toxicity during the first and second courses of high-dose methotrexate. 31607921 2019
CUI: C0686377
Disease: CNS metastases
CNS metastases
0.010 Biomarker phenotype BEFREE On the whole, these results provide an approach for addressing the mechanisms of BCR‑ABL1+ B‑ALL with CNS metastasis and may guide the development of novel therapeutic strategies. 31173268 2019
CUI: C1328504
Disease: Hormone refractory prostate cancer
Hormone refractory prostate cancer
0.010 Biomarker disease BEFREE We set the starting point at the timing of BCR, and the endpoints were development to castration-resistant prostate cancer (CRPC) and cancer-specific death. 31559475 2019
Primary Cutaneous Follicle Center Lymphoma
0.010 Biomarker disease BEFREE Similar to FL but in contrast to primary cutaneous diffuse large B-cell lymphoma, leg-type, BCR genes of 15 PCFCLs (83%) had acquired N-linked glycosylation motifs. 31042459 2019
CUI: C1883018
Disease: Severe Aplastic Anemia
Severe Aplastic Anemia
0.010 Biomarker disease BEFREE Sixteen patients (76.2%) were diagnosed with ALL and the rest individually with AML, CML, T-lymphoma, Burkitt lymphoma, and severe aplastic anemia. 31521834 2019
CUI: C2717961
Disease: Thrombotic Microangiopathies
Thrombotic Microangiopathies
0.010 GeneticVariation group BEFREE Thrombotic microangiopathy as a cause of cardiovascular toxicity from the BCR-ABL1 tyrosine kinase inhibitor ponatinib. 30692122 2019
CHROMOSOME 8p11 MYELOPROLIFERATIVE SYNDROME
0.010 Biomarker disease BEFREE Collectively, these data show that the BCR GEF domain affects phenotypes associated with progression of SCLL through suppression of RHOA signaling. 30413411 2019
Infant Acute Undifferentiated Leukemia
0.010 Biomarker disease BEFREE Of the total 631 cases, 52.9% (n=334) were acute lymphoblastic leukemia (ALL), 43.9% (n=277) acute myeloid leukemia (AML), 2.2% (n=14) mixed phenotypic acute leukemia (MPAL), 0.5% (n=3) acute undifferentiated leukemia (AUL) and 0.5% (n=3) chronic myeloid leukemia in blast crisis (CML-BC). 30858955 2019
CUI: C4324336
Disease: Hyperleukocytosis
Hyperleukocytosis
0.010 Biomarker disease BEFREE Leukocytapheresis procedures were performed in 192 leukemia patients (including acute myeloid leukemia [AML], acute lymphoblastic leukemia [ALL], and chronic myeloid leukemia [CML]) with hyperleukocytosis between January and December 2016. 31829470 2019
CUI: C4554344
Disease: IgE-mediated food allergy
IgE-mediated food allergy
0.010 Biomarker disease BEFREE CML) than that in the cases of glucose and maltose; therefore, maltotriose could be applied to desensitize TM-induced food allergy through glycation, and this could be a potential immunotherapy for shrimp allergy patients. 31580362 2019
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.010 Biomarker disease BEFREE These results suggest that Psen1 functions as a scaffold of the BCR-CK2α-p65 complex and that this signaling cascade could be a novel therapeutic target for various chronic inflammation conditions, including those in Alzheimer disease. 30201812 2018
CUI: C0017661
Disease: IGA Glomerulonephritis
IGA Glomerulonephritis
0.010 AlteredExpression disease BEFREE The present results revealed that the BCR/TCR CDR3 clones were expressed at very low frequencies, and the composition of clone types in patients with IgAN was skewed; the majority of clones were unique, and only 12 BCR and 228 TCR CDR3 clones were public ones, of which 16 were expressed at a significantly higher frequency in patients with IgAN (P<0.001). 29568935 2018
CUI: C0028081
Disease: Night sweats
Night sweats
0.010 Biomarker phenotype BEFREE A 73-year-old man presenting with fatigue and drenching night sweats lasting for 2 weeks was diagnosed with chronic myeloid leukemia based on an analysis of a bone marrow biopsy and detection of the BCR-ABL1 fusion gene in peripheral blood. 30419862 2018
CUI: C0032227
Disease: Pleural effusion disorder
Pleural effusion disorder
0.010 GeneticVariation group BEFREE We identified 196 cases of PE in a series of 853 CML-CP DAS-treated patients (incidence 23.0%). 28971265 2018