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 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 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 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 RET activation by germline MEN2A and MEN2B mutations. 8570194 1995
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 Biological and biochemical properties of Ret with kinase domain mutations identified in multiple endocrine neoplasia type 2B and familial medullary thyroid carcinoma. 10445857 1999