RARA, retinoic acid receptor alpha, 5914

N. diseases: 274; N. variants: 3
Disease: Fibroadenoma ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0206650
Disease: Fibroadenoma
Fibroadenoma 		0.330 GeneticVariation disease BEFREE Compared to FAs, PTs had significantly higher mutation rates in the TERT promoter (p <  0.001), RARA (p <  0.001), FLNA, RB1 and TP53 (p = 0.002, 0.020 and 0.018, respectively). 31647027 2019
CUI: C0206650
Disease: Fibroadenoma
Fibroadenoma 		0.330 GeneticVariation disease BEFREE First, we frequently observed MED12 and RARA mutations in both fibroadenomas and phyllodes tumors, emphasizing the importance of these mutations in fibroepithelial tumorigenesis. 26437033 2015
CUI: C0206650
Disease: Fibroadenoma
Fibroadenoma 		0.330 Biomarker disease CTD_human First, we frequently observed MED12 and RARA mutations in both fibroadenomas and phyllodes tumors, emphasizing the importance of these mutations in fibroepithelial tumorigenesis. 26437033 2015
CUI: C0206650
Disease: Fibroadenoma
Fibroadenoma 		0.330 AlteredExpression disease BEFREE Our findings showed that RAR-β2 expression was lower in the breast cancer compared to normal tissue and fibroadenoma. 20865461 2011