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 		0.100 CausalMutation phenotype CLINVAR Pheochromocytoma and paraganglioma: understanding the complexities of the genetic background. 22429592 2012
Entrez Id: 5979
Gene Symbol: RET
RET 		0.100 CausalMutation phenotype CLINVAR Multiple endocrine neoplasias type 2B and RET proto-oncogene. 22429913 2012
Entrez Id: 5979
Gene Symbol: RET
RET 		0.100 CausalMutation phenotype CLINVAR Genetics and clinical characteristics of hereditary pheochromocytomas and paragangliomas. 22041710 2011
Entrez Id: 5979
Gene Symbol: RET
RET 		0.100 CausalMutation phenotype CLINVAR Update multiple endocrine neoplasia type 2. 20087666 2010
Entrez Id: 5979
Gene Symbol: RET
RET 		0.100 CausalMutation phenotype CLINVAR Medullary thyroid cancer: management guidelines of the American Thyroid Association. 19469690 2009
Entrez Id: 5979
Gene Symbol: RET
RET 		0.100 CausalMutation phenotype CLINVAR Hirschsprung disease, associated syndromes and genetics: a review. 17965226 2008
Entrez Id: 5979
Gene Symbol: RET
RET 		0.100 CausalMutation phenotype CLINVAR Pheochromocytoma penetrance varies by RET mutation in MEN 2A. 18063059 2007
Entrez Id: 5979
Gene Symbol: RET
RET 		0.100 CausalMutation phenotype CLINVAR Germ-line mutations in nonsyndromic pheochromocytoma. 12000816 2002
Entrez Id: 5979
Gene Symbol: RET
RET 		0.100 CausalMutation phenotype CLINVAR Mutations of the RET proto-oncogene in the multiple endocrine neoplasia type 2 syndromes, related sporadic tumours, and hirschsprung disease. 9067749 1997
Entrez Id: 5979
Gene Symbol: RET
RET 		0.100 CausalMutation phenotype CLINVAR The relationship between specific RET proto-oncogene mutations and disease phenotype in multiple endocrine neoplasia type 2. International RET mutation consortium analysis. 8918855 1996
Entrez Id: 5979
Gene Symbol: RET
RET 		0.100 CausalMutation phenotype CLINVAR Diverse phenotypes associated with exon 10 mutations of the RET proto-oncogene. 7881414 1994
Entrez Id: 5979
Gene Symbol: RET
RET 		0.100 CausalMutation phenotype CLINVAR Single missense mutation in the tyrosine kinase catalytic domain of the RET protooncogene is associated with multiple endocrine neoplasia type 2B. 7906417 1994
Entrez Id: 5979
Gene Symbol: RET
RET 		0.100 Biomarker phenotype HPO