Gene: MSH6 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 2956
Gene Symbol: MSH6
MSH6 		0.030 AlteredExpression disease BEFREE This is the first report of two somatic MSH2 mutations leading to an MSI-H tumour lacking MSH2-MSH6 protein expression in a patient with MAP. 24518836 2014
Entrez Id: 2956
Gene Symbol: MSH6
MSH6 		0.030 GeneticVariation disease BEFREE Here, we characterize one newly identified MAP-associated MYH missense mutation (R231L) that lies adjacent to the putative hMSH6 binding domain. 17081686 2007
Entrez Id: 2956
Gene Symbol: MSH6
MSH6 		0.030 GeneticVariation disease BEFREE Most recently, MYH-associated polyposis (MAP) and an "atypical Lynch syndrome" related to the presence of MSH6 mutations have been linked to an increased risk of CRC. 17920897 2007