MED12, mediator complex subunit 12, 9968

N. diseases: 340; N. variants: 21
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1458155
Disease: Mammary Neoplasms
Mammary Neoplasms
0.430 GeneticVariation group CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
CUI: C1458155
Disease: Mammary Neoplasms
Mammary Neoplasms
0.430 GeneticVariation group BEFREE Mutational analysis of MED12 exon 2 in a spectrum of fibroepithelial tumours of the breast: implications for pathogenesis and histogenesis. 26109290 2016
CUI: C1458155
Disease: Mammary Neoplasms
Mammary Neoplasms
0.430 Biomarker group CTD_human Exome sequencing identifies highly recurrent MED12 somatic mutations in breast fibroadenoma. 25038752 2014
CUI: C1458155
Disease: Mammary Neoplasms
Mammary Neoplasms
0.430 GeneticVariation group BEFREE MED12 mutations were frequent among the phyllodes tumours of the breast, regardless of the tumour grade. 25839987 2015
CUI: C1458155
Disease: Mammary Neoplasms
Mammary Neoplasms
0.430 Biomarker group CTD_human Genomic landscapes of breast fibroepithelial tumors. 26437033 2015
CUI: C1458155
Disease: Mammary Neoplasms
Mammary Neoplasms
0.430 GeneticVariation group BEFREE MED12 somatic mutations in fibroadenomas and phyllodes tumours of the breast. 25855048 2015