HRAS, HRas proto-oncogene, GTPase, 3265

N. diseases: 698; N. variants: 29
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0040136
Disease: Thyroid Neoplasm
Thyroid Neoplasm
0.460 GeneticVariation disease CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
CUI: C0040136
Disease: Thyroid Neoplasm
Thyroid Neoplasm
0.460 Biomarker disease BEFREE Some somatic oncogene mutations (BRAF, NRAS, HRAS, KRAS) as well as gene translocations (RET/PTC, PAX8/PPAR-gamma) have been associated with the development of thyroid cancer. 26259532 2016
CUI: C0040136
Disease: Thyroid Neoplasm
Thyroid Neoplasm
0.460 CausalMutation disease CLINVAR Prospective enterprise-level molecular genotyping of a cohort of cancer patients. 25157968 2014
CUI: C0040136
Disease: Thyroid Neoplasm
Thyroid Neoplasm
0.460 CausalMutation disease CLINVAR Selumetinib-enhanced radioiodine uptake in advanced thyroid cancer. 23406027 2013
CUI: C0040136
Disease: Thyroid Neoplasm
Thyroid Neoplasm
0.460 GeneticVariation disease BEFREE No mutation was found in any of the thyroid tumor tissue samples, but we frequently detected polymorphism at nucleotide 81 (T > C) in exon 1 of HRAS gene. 23150177 2013
CUI: C0040136
Disease: Thyroid Neoplasm
Thyroid Neoplasm
0.460 CausalMutation disease CLINVAR Phase II trial of sorafenib in metastatic thyroid cancer. 19255327 2009
CUI: C0040136
Disease: Thyroid Neoplasm
Thyroid Neoplasm
0.460 CausalMutation disease CLINVAR Beneficial effects of sorafenib on tumor progression, but not on radioiodine uptake, in patients with differentiated thyroid carcinoma. 19773371 2009
CUI: C0040136
Disease: Thyroid Neoplasm
Thyroid Neoplasm
0.460 GeneticVariation disease LHGDN BRAF and K-RAS mutation in a Greek papillary and medullary thyroid carcinoma cohort. 18383861 2008
CUI: C0040136
Disease: Thyroid Neoplasm
Thyroid Neoplasm
0.460 GeneticVariation disease LHGDN Familial non-medullary thyroid carcinoma (FNMTC): analysis of fPTC/PRN, NMTC1, MNG1 and TCO susceptibility loci and identification of somatic BRAF and RAS mutations. 18310288 2008
CUI: C0040136
Disease: Thyroid Neoplasm
Thyroid Neoplasm
0.460 CausalMutation disease CLINVAR Hyperactive Ras in developmental disorders and cancer. 17384584 2007
CUI: C0040136
Disease: Thyroid Neoplasm
Thyroid Neoplasm
0.460 GeneticVariation disease BEFREE Using polymerase chain reaction and sequence-specific oligonucleotide hybridization, the frequency of three ras oncogene mutations (N-ras, Ha-ras, and K-ras) in thyroid tumors (25 adenomas, 16 follicular carcinomas, and 22 papillary carcinomas) was investigated in both iodide-deficient and iodide-sufficient areas. 2021946 1991
CUI: C0040136
Disease: Thyroid Neoplasm
Thyroid Neoplasm
0.460 GeneticVariation disease BEFREE Thus the a4 and a2 alleles of c-Ha-ras-1 may perhaps be viewed as genetic markers of predisposition to lung, ovarian and thyroid cancer, respectively, in combination with other clinical parameters. 1980342 1990
CUI: C0040136
Disease: Thyroid Neoplasm
Thyroid Neoplasm
0.460 Biomarker disease CTD_human Agent-specific ras oncogene activation in rat thyroid tumours. 3078959 1988