Gene: RET ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 5979
Gene Symbol: RET
RET 		0.020 GeneticVariation phenotype LHGDN Absence of RET gene point mutations in sporadic thyroid C-cell hyperplasia. 17384213 2007
Entrez Id: 5979
Gene Symbol: RET
RET 		0.020 GeneticVariation phenotype LHGDN In order to study the relationship between a misfunctioning of the RET proto-oncogene and the presence of C-cell hyperplasia, we compared a series of thyroid glands presenting sporadic or radiation-associated tumours, as well as samples of unrelated normal thyroid tissues, for alteration in exons 10 and 11 of the gene and for the presence or absence of C-cell hyperplasia. 12085189 2002