Gene: CDC73 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 79577
Gene Symbol: CDC73
CDC73 		0.400 GeneticVariation disease BEFREE Parafibromin mutations in hereditary hyperparathyroidism syndromes and parathyroid tumours. 16487440 2006
Entrez Id: 79577
Gene Symbol: CDC73
CDC73 		0.400 Biomarker disease BEFREE Inactivation of the HRPT2/CDC73 gene, encoding the putative tumor-suppressor protein parafibromin and discovered in the context of the hyperparathyroidism-jaw tumor (HPT-JT) syndrome, is a common, somatic event in most parathyroid cancers. 21167377 2010
Entrez Id: 79577
Gene Symbol: CDC73
CDC73 		0.400 GeneticVariation disease BEFREE <i>Parathyroid carcinoma.</i> Most parathyroid carcinomas are functional, resulting in hyperparathyroidism and a high serum calcium level; however, non-functioning parathyroid carcinomas are also rarely described in individuals with a <i>CDC73-</i>related disorder. 29692167 2018
Entrez Id: 79577
Gene Symbol: CDC73
CDC73 		0.400 GeneticVariation disease BEFREE CDC73-related hereditary hyperparathyroidism: five new mutations and the clinical spectrum. 21652691 2011
Entrez Id: 79577
Gene Symbol: CDC73
CDC73 		0.400 GeneticVariation disease LHGDN Human gene mutations. Gene symbol: HRPT2. Disease: Hyperparathyroidism Jaw-tumor syndrome. 15046094 2004
Entrez Id: 79577
Gene Symbol: CDC73
CDC73 		0.400 GeneticVariation disease LHGDN Germline and de novo mutations in the HRPT2 tumour suppressor gene in familial isolated hyperparathyroidism (FIHP). 14985403 2004
Entrez Id: 79577
Gene Symbol: CDC73
CDC73 		0.400 GeneticVariation disease LHGDN Human gene mutations. Gene symbol: HRPT2. Disease: Hyperparathyroidism Jaw-tumor syndrome. 15046050 2004
Entrez Id: 79577
Gene Symbol: CDC73
CDC73 		0.400 GeneticVariation disease LHGDN Genetic testing in familial isolated hyperparathyroidism: unexpected results and their implications. 14985373 2004
Entrez Id: 79577
Gene Symbol: CDC73
CDC73 		0.400 GeneticVariation disease LHGDN Familial isolated hyperparathyroidism is rarely caused by germline mutation in HRPT2, the gene for the hyperparathyroidism-jaw tumor syndrome. 14715834 2004
Entrez Id: 79577
Gene Symbol: CDC73
CDC73 		0.400 GeneticVariation disease LHGDN Human gene mutations. Gene symbol: HRPT2. Disease: Hyperparathyroidism Jaw-tumor syndrome. 15046105 2004
Entrez Id: 79577
Gene Symbol: CDC73
CDC73 		0.400 GeneticVariation disease LHGDN Human gene mutations. Gene symbol: HRPT2. Disease: Hyperparathyroidism Jaw-tumor syndrome. 15046098 2004
Entrez Id: 79577
Gene Symbol: CDC73
CDC73 		0.400 GeneticVariation disease LHGDN Human gene mutations. Gene symbol: HRPT2. Disease: Hyperparathyroidism Jaw-tumor syndrome. 15046109 2004
Entrez Id: 79577
Gene Symbol: CDC73
CDC73 		0.400 GeneticVariation disease LHGDN Human gene mutations. Gene symbol: HRPT2. Disease: Hyperparathyroidism Jaw-tumor syndrome. 15046102 2004
Entrez Id: 79577
Gene Symbol: CDC73
CDC73 		0.400 GeneticVariation disease LHGDN An unacceptable recurrence/persistence rate (80%) associated with increasingly difficult re-operations and risk of parathyroid carcinoma in the setting of germline mutations of HRPT2 gene with familial hyperparathyroidism suggest that a more aggressive operative approach should be undertaken in these patients. 18436011 2008
Entrez Id: 79577
Gene Symbol: CDC73
CDC73 		0.400 GeneticVariation disease LHGDN Human gene mutations. Gene symbol: HRPT2. Disease: Hyperparathyroidism Jaw-tumor syndrome. 15046107 2004
Entrez Id: 79577
Gene Symbol: CDC73
CDC73 		0.400 Biomarker disease MGD Mice deleted for cell division cycle 73 gene develop parathyroid and uterine tumours: model for the hyperparathyroidism-jaw tumour syndrome. 28288139 2017
Entrez Id: 79577
Gene Symbol: CDC73
CDC73 		0.400 Biomarker disease HPO