RARG, retinoic acid receptor gamma, 5916

N. diseases: 62; N. variants: 3
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0876994
Disease: Cardiotoxicity
Cardiotoxicity
0.400 Biomarker disease CTD_human A coding variant in RARG confers susceptibility to anthracycline-induced cardiotoxicity in childhood cancer. 26237429 2015
CUI: C0876994
Disease: Cardiotoxicity
Cardiotoxicity
0.400 GeneticVariation disease GWASCAT A coding variant in RARG confers susceptibility to anthracycline-induced cardiotoxicity in childhood cancer. 26237429 2015
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.330 AlteredExpression disease BEFREE Pre-clinical observation highlighted that triple negative (estrogen receptor/progesterone receptor/human epidermal growth factor receptor)-breast cancer cells displayed resistance to retinoids due to the RARγ high expression profile. 29849791 2018
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.330 Biomarker disease BEFREE Potential role for retinoic acid receptor-gamma in the inhibition of breast cancer cells by selective retinoids and interferons. 8603404 1996
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.330 AlteredExpression disease BEFREE The functional consequence of the interplay between c-Myc oncogene expression and the RARγ to RARα/β balance suggests that prevalence of RARγ over-RARα/β expression levels in breast cancer accompanied by c-Myc amplification or over-expression in breast cancer should be predictive of response to treatment with RARα-isotype-specific agonists and warrant monitoring during clinical trials. 22920668 2012
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.330 GeneticVariation disease UNIPROT
CUI: C0008925
Disease: Cleft Palate
Cleft Palate
0.300 Biomarker disease CTD_human Retinoic acid drives aryl hydrocarbon receptor expression and is instrumental to dioxin-induced toxicity during palate development. 21807577 2011
CUI: C1837218
Disease: Cleft palate, isolated
Cleft palate, isolated
0.300 Biomarker disease CTD_human Retinoic acid drives aryl hydrocarbon receptor expression and is instrumental to dioxin-induced toxicity during palate development. 21807577 2011
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.110 GeneticVariation disease GWASCAT Pleiotropic Meta-Analysis of Cognition, Education, and Schizophrenia Differentiates Roles of Early Neurodevelopmental and Adult Synaptic Pathways. 31374203 2019
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.110 AlteredExpression disease BEFREE We detected decreased expression of RARG and NR4A2 mRNAs in females with schizophrenia (p<0.05). 27992436 2016
CUI: C0278704
Disease: Malignant Childhood Neoplasm
Malignant Childhood Neoplasm
0.110 GeneticVariation disease GWASCAT A coding variant in RARG confers susceptibility to anthracycline-induced cardiotoxicity in childhood cancer. 26237429 2015
CUI: C0278704
Disease: Malignant Childhood Neoplasm
Malignant Childhood Neoplasm
0.110 GeneticVariation disease BEFREE A coding variant in RARG confers susceptibility to anthracycline-induced cardiotoxicity in childhood cancer. 26237429 2015
CUI: C0023418
Disease: leukemia
leukemia
0.040 Biomarker disease LHGDN A redundant oncogenic potential of the retinoic receptor (RAR) alpha, beta and gamma isoforms in acute promyelocytic leukemia. 17252005 2007
CUI: C0023418
Disease: leukemia
leukemia
0.040 GeneticVariation disease BEFREE Critical role of retinoid/rexinoid signaling in mediating transformation and therapeutic response of NUP98-RARG leukemia. 25510432 2015
CUI: C0023418
Disease: leukemia
leukemia
0.040 Biomarker disease BEFREE The regulation of the subcellular content of CDK1 and RARγ by ATRA is an important process for achieving an effective response in treatment of leukemia. 23518499 2013
CUI: C0023418
Disease: leukemia
leukemia
0.040 GeneticVariation disease BEFREE RARA and RARG gene downregulation associated with EZH2 mutation in acute promyelocytic-like morphology leukemia. 29530751 2018
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
0.040 Biomarker disease BEFREE RARG Gene Dysregulation in Acute Myeloid Leukemia. 31709264 2019
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
0.040 Biomarker disease BEFREE CDK1 interacts with RARγ and plays an important role in treatment response of acute myeloid leukemia. 23518499 2013
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
0.040 Biomarker disease BEFREE A novel NPM1-RARG-NPM1 chimeric fusion in acute myeloid leukaemia resembling acute promyelocytic leukaemia but resistant to all-trans retinoic acid and arsenic trioxide. 30996344 2019
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
0.040 Biomarker disease BEFREE A novel NUP98/RARG gene fusion in acute myeloid leukemia resembling acute promyelocytic leukemia. 20935257 2011
CUI: C0023487
Disease: Acute Promyelocytic Leukemia
Acute Promyelocytic Leukemia
0.040 GeneticVariation disease BEFREE We hypothesize a novel mechanism of EZH2 function alteration, which may be responsible for an acute myeloid leukemia with APL-like phenotype featuring dysregulation of the RARA and RARG genes. 29530751 2018
CUI: C0023487
Disease: Acute Promyelocytic Leukemia
Acute Promyelocytic Leukemia
0.040 Biomarker disease BEFREE These uncovered fusion genes strongly suggested their contributions to leukemogenesis as driver alternations and APL phenotype may arise by abnormalities of other members of the nuclear receptor superfamily involved in retinoid signaling (RARB or RARG) or even by mechanisms distinct from the formation of aberrant retinoid receptors. 30575821 2019
CUI: C0023487
Disease: Acute Promyelocytic Leukemia
Acute Promyelocytic Leukemia
0.040 Biomarker disease BEFREE A novel NUP98/RARG gene fusion in acute myeloid leukemia resembling acute promyelocytic leukemia. 20935257 2011
CUI: C0023487
Disease: Acute Promyelocytic Leukemia
Acute Promyelocytic Leukemia
0.040 Biomarker disease BEFREE RARG fusion is rare but recurrent in APL, further investigation in larger cohorts is expected to assess frequency, clinical characteristics and outcomes of RARG-translocation in APL. 30996344 2019
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.030 AlteredExpression disease BEFREE The functional consequence of the interplay between c-Myc oncogene expression and the RARγ to RARα/β balance suggests that prevalence of RARγ over-RARα/β expression levels in breast cancer accompanied by c-Myc amplification or over-expression in breast cancer should be predictive of response to treatment with RARα-isotype-specific agonists and warrant monitoring during clinical trials. 22920668 2012