Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 5979
Gene Symbol: RET
RET
0.100 GeneticVariation disease CLINVAR RET-familial medullary thyroid carcinoma mutants Y791F and S891A activate a Src/JAK/STAT3 pathway, independent of glial cell line-derived neurotrophic factor. 15753368 2005
Entrez Id: 5979
Gene Symbol: RET
RET
0.100 GeneticVariation disease CLINVAR The Glu632-Leu633 deletion in cysteine rich domain of Ret induces constitutive dimerization and alters the processing of the receptor protein. 10490816 1999
Entrez Id: 5979
Gene Symbol: RET
RET
0.100 GeneticVariation disease CLINVAR Biological and biochemical properties of Ret with kinase domain mutations identified in multiple endocrine neoplasia type 2B and familial medullary thyroid carcinoma. 10445857 1999
Entrez Id: 5979
Gene Symbol: RET
RET
0.100 GeneticVariation disease CLINVAR The different RET-activating capability of mutations of cysteine 620 or cysteine 634 correlates with the multiple endocrine neoplasia type 2 disease phenotype. 9012462 1997
Entrez Id: 5979
Gene Symbol: RET
RET
0.100 GeneticVariation disease CLINVAR Oncogenic activation of RET by two distinct FMTC mutations affecting the tyrosine kinase domain. 9242375 1997
Entrez Id: 5979
Gene Symbol: RET
RET
0.100 GeneticVariation disease CLINVAR RET activation by germline MEN2A and MEN2B mutations. 8570194 1995