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 Biomarker disease BEFREE The HRPT2 (hereditary hyperparathyroidism type 2) tumor suppressor gene encodes a ubiquitously expressed 531 amino acid protein termed parafibromin. 16989776 2006
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 GeneticVariation disease BEFREE Parafibromin is the 531-amino-acid protein product encoded by HRPT2, a putative tumor suppressor gene recently implicated in the autosomal dominant hyperparathyroidism-jaw tumor familial cancer syndrome, sporadic parathyroid cancer, and a minority of families with isolated hyperparathyroidism. 15580289 2005
Entrez Id: 79577
Gene Symbol: CDC73
CDC73 		0.400 GeneticVariation disease BEFREE Hyperparathyroidism-jaw tumor (HPT-JT) syndrome is a familial multi-tumor syndrome resulting from mutations in the HRPT2 tumor suppressor gene, which encodes a protein product named parafibromin. 15579037 2004
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 Human gene mutations. Gene symbol: HRPT2. Disease: Hyperparathyroidism Jaw-tumor syndrome. 15046107 2004
Entrez Id: 79577
Gene Symbol: CDC73
CDC73 		0.400 Biomarker disease BEFREE Familial isolated hyperparathyroidism maps to the hyperparathyroidism-jaw tumor locus in 1q21-q32 in a subset of families. 9626148 1998
Entrez Id: 79577
Gene Symbol: CDC73
CDC73 		0.400 GeneticVariation disease BEFREE The HRPT 2 gene responsible for the development of hereditary hyperparathyroidism and jaw tumors has been localized on the 1q21-31 locus. 9736402 1998
Entrez Id: 79577
Gene Symbol: CDC73
CDC73 		0.400 Biomarker disease HPO