×
Entrez Id: 5979
Gene Symbol: RET
RET
Neoplastic Syndromes, Hereditary
0.200
CausalMutation
CLINVAR
Impact of RET proto-oncogene analysis on the clinical management of multiple endocrine neoplasia type 2.
16532227 2006
×
Entrez Id: 5979
Gene Symbol: RET
RET
Neoplastic Syndromes, Hereditary
0.200
CausalMutation
CLINVAR
Functional characterization of the MTC-associated germline RET-K666E mutation: evidence of oncogenic potential enhanced by the G691S polymorphism.
21690267 2011
×
Entrez Id: 5979
Gene Symbol: RET
RET
Neoplastic Syndromes, Hereditary
0.200
CausalMutation
CLINVAR
Different RET gene mutation-induced multiple endocrine neoplasia type 2A in 3 Chinese families.
28099363 2017
×
Entrez Id: 5979
Gene Symbol: RET
RET
Neoplastic Syndromes, Hereditary
0.200
CausalMutation
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
Neoplastic Syndromes, Hereditary
0.200
CausalMutation
CLINVAR
The occurrence and the type of germline mutations in the RET gene in patients with medullary thyroid carcinoma and their unaffected kindred's from Central Poland.
18058472 2007
×
Entrez Id: 5979
Gene Symbol: RET
RET
Neoplastic Syndromes, Hereditary
0.200
CausalMutation
CLINVAR
Hereditary medullary thyroid cancer in Slovenia--genotype-phenotype correlations.
16865646 2006
×
Entrez Id: 5979
Gene Symbol: RET
RET
Neoplastic Syndromes, Hereditary
0.200
CausalMutation
CLINVAR
RET genetic screening in patients with medullary thyroid cancer and their relatives: experience with 807 individuals at one center.
17895320 2007
×
Entrez Id: 5979
Gene Symbol: RET
RET
Neoplastic Syndromes, Hereditary
0.200
CausalMutation
CLINVAR
Sporadic versus familial medullary thyroid microcarcinoma: a histopathologic study of 50 consecutive patients.
11688458 2001
×
Entrez Id: 5979
Gene Symbol: RET
RET
Neoplastic Syndromes, Hereditary
0.200
CausalMutation
CLINVAR
Papillary thyroid carcinoma in patients with RET proto-oncogene germline mutation.
12193298 2002
×
Entrez Id: 5979
Gene Symbol: RET
RET
Neoplastic Syndromes, Hereditary
0.200
CausalMutation
CLINVAR
Germline mutations and genotype-phenotype correlation in Asian Indian patients with pheochromocytoma and paraganglioma.
27539324 2016
×
Entrez Id: 5979
Gene Symbol: RET
RET
Neoplastic Syndromes, Hereditary
0.200
CausalMutation
CLINVAR
Mechanism of Ret activation by a mutation at aspartic acid 631 identified in sporadic pheochromocytoma.
10049754 1999
×
Entrez Id: 5979
Gene Symbol: RET
RET
Neoplastic Syndromes, Hereditary
0.200
CausalMutation
CLINVAR
Bilateral adrenal pheochromocytoma with a germline L790F mutation in the RET oncogene.
22403753 2012
×
Entrez Id: 5979
Gene Symbol: RET
RET
Neoplastic Syndromes, Hereditary
0.200
CausalMutation
CLINVAR
A rare extracellular D631Y germline mutation of the RET proto-oncogene in two Korean families with multiple endocrine neoplasia 2A.
16839264 2006
×
Entrez Id: 5979
Gene Symbol: RET
RET
Neoplastic Syndromes, Hereditary
0.200
CausalMutation
CLINVAR
Distribution of RET Mutations in Multiple Endocrine Neoplasia 2 in Denmark 1994-2014: A Nationwide Study.
27809725 2017
×
Entrez Id: 5979
Gene Symbol: RET
RET
Neoplastic Syndromes, Hereditary
0.200
CausalMutation
CLINVAR
RET proto-oncogene mutations in French MEN 2A and FMTC families.
7874109 1994
×
Entrez Id: 5979
Gene Symbol: RET
RET
Neoplastic Syndromes, Hereditary
0.200
CausalMutation
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
Neoplastic Syndromes, Hereditary
0.200
CausalMutation
CLINVAR
Indolent medullary thyroid cancer with a RET proto-oncogene Cys618Phe mutation presenting as sporadic unilateral pheochromocytoma in a 55-year-old Korean woman.
21254918 2011
×
Entrez Id: 5979
Gene Symbol: RET
RET
Neoplastic Syndromes, Hereditary
0.200
CausalMutation
CLINVAR
In silico and in vitro analysis of rare germline allelic variants of RET oncogene associated with medullary thyroid cancer.
21810974 2011
×
Entrez Id: 5979
Gene Symbol: RET
RET
Neoplastic Syndromes, Hereditary
0.200
CausalMutation
CLINVAR
Homozygosity for a frequent and weakly penetrant predisposing allele at the RET locus in sporadic Hirschsprung disease.
15744028 2005
×
Entrez Id: 5979
Gene Symbol: RET
RET
Neoplastic Syndromes, Hereditary
0.200
CausalMutation
CLINVAR
Failure of pentagastrin-stimulated calcitonin testing in early manifestation of familial medullary thyroid cancer.
22965292 2012
×
Entrez Id: 5979
Gene Symbol: RET
RET
Neoplastic Syndromes, Hereditary
0.200
CausalMutation
CLINVAR
Familial prevalence and age of RET germline mutations: implications for screening.
18062802 2008
×
Entrez Id: 5979
Gene Symbol: RET
RET
Neoplastic Syndromes, Hereditary
0.200
CausalMutation
CLINVAR
Hirschsprung's disease and medullary thyroid carcinoma: 15-year experience with molecular genetic screening of the RET proto-oncogene.
21986619 2012
×
Entrez Id: 5979
Gene Symbol: RET
RET
Neoplastic Syndromes, Hereditary
0.200
CausalMutation
CLINVAR
A novel point mutation in the intracellular domain of the ret protooncogene in a family with medullary thyroid carcinoma.
9398735 1997
×
Entrez Id: 5979
Gene Symbol: RET
RET
Neoplastic Syndromes, Hereditary
0.200
CausalMutation
CLINVAR
Germ-line mutations in nonsyndromic pheochromocytoma.
12000816 2002
×
Entrez Id: 5979
Gene Symbol: RET
RET
Neoplastic Syndromes, Hereditary
0.200
CausalMutation
CLINVAR
Role of prophylactic thyroidectomy in RET 790 familial medullary thyroid carcinoma.
21688339 2012