MIR146A, microRNA 146a, 406938

N. diseases: 505; N. variants: 3
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0740302
Disease: 5q-syndrome
5q-syndrome
0.060 AlteredExpression disease BEFREE Rps14, Csnk1a1 and miRNA145/miRNA146a deficiency cooperate in the clinical phenotype and activation of the innate immune system in the 5q- syndrome. 30651631 2019
CUI: C0740302
Disease: 5q-syndrome
5q-syndrome
0.060 Biomarker disease BEFREE Recent evidence suggests that haploinsufficiency of the microRNA genes miR-145 and miR-146a may contribute to the thrombocytosis seen in the 5q- syndrome. 22571696 2012
CUI: C0740302
Disease: 5q-syndrome
5q-syndrome
0.060 GeneticVariation disease BEFREE The megakaryocytic and platelet phenotype of the 5q-syndrome has been attributed to heterozygous deletion of miR145 and miR146a. 21943668 2011
CUI: C0740302
Disease: 5q-syndrome
5q-syndrome
0.060 Biomarker disease BEFREE Identification of miR-145 and miR-146a as mediators of the 5q- syndrome phenotype. 19898489 2010
CUI: C0740302
Disease: 5q-syndrome
5q-syndrome
0.060 Biomarker disease BEFREE Other mouse modeling data suggest that haploinsufficiency of the microRNA genes miR-145 and miR-146a may contribute to the thrombocytosis seen in the 5q- syndrome. 20733155 2010
CUI: C0740302
Disease: 5q-syndrome
5q-syndrome
0.060 Biomarker disease BEFREE Identification of miR-145 and miR-146a as mediators of the 5q- syndrome phenotype.Nat.Med.16(1), 49-58 (2009). 20469997 2010