Source: GWASCAT

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 81037
Gene Symbol: CLPTM1L
CLPTM1L
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung 		0.200 GeneticVariation GWASCAT Common 5p15.33 and 6p21.33 variants influence lung cancer risk. 18978787

2008
Entrez Id: 81037
Gene Symbol: CLPTM1L
CLPTM1L
CUI: C0007117
Disease: Basal cell carcinoma
Basal cell carcinoma 		0.100 GeneticVariation GWASCAT Sequence variants at the TERT-CLPTM1L locus associate with many cancer types. 19151717

2009
Entrez Id: 81037
Gene Symbol: CLPTM1L
CLPTM1L
CUI: C0206710
Disease: Basal Cell Neoplasm
Basal Cell Neoplasm 		0.100 GeneticVariation GWASCAT Sequence variants at the TERT-CLPTM1L locus associate with many cancer types. 19151717

2009
Entrez Id: 81037
Gene Symbol: CLPTM1L
CLPTM1L
CUI: C0751676
Disease: Basal Cell Cancer
Basal Cell Cancer 		0.100 GeneticVariation GWASCAT Sequence variants at the TERT-CLPTM1L locus associate with many cancer types. 19151717

2009
Entrez Id: 81037
Gene Symbol: CLPTM1L
CLPTM1L
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
Adenocarcinoma of lung (disorder) 		0.460 GeneticVariation GWASCAT A genome-wide association study of lung cancer identifies a region of chromosome 5p15 associated with risk for adenocarcinoma. 19836008

2009
Entrez Id: 81037
Gene Symbol: CLPTM1L
CLPTM1L
CUI: C0235974
Disease: Pancreatic carcinoma
Pancreatic carcinoma 		0.160 GeneticVariation GWASCAT A genome-wide association study identifies pancreatic cancer susceptibility loci on chromosomes 13q22.1, 1q32.1 and 5p15.33. 20101243

2010
Entrez Id: 81037
Gene Symbol: CLPTM1L
CLPTM1L
CUI: C0699885
Disease: Carcinoma of bladder
Carcinoma of bladder 		0.100 GeneticVariation GWASCAT A multi-stage genome-wide association study of bladder cancer identifies multiple susceptibility loci. 20972438

2010
Entrez Id: 81037
Gene Symbol: CLPTM1L
CLPTM1L
CUI: C0201544
Disease: Prostate specific antigen measurement
Prostate specific antigen measurement 		0.100 GeneticVariation GWASCAT Genetic correction of PSA values using sequence variants associated with PSA levels. 21160077

2010
Entrez Id: 81037
Gene Symbol: CLPTM1L
CLPTM1L
CUI: C0025202
Disease: melanoma
melanoma 		0.160 GeneticVariation GWASCAT Genome-wide association study identifies three new melanoma susceptibility loci. 21983787

2011
Entrez Id: 81037
Gene Symbol: CLPTM1L
CLPTM1L
CUI: C0699885
Disease: Carcinoma of bladder
Carcinoma of bladder 		0.100 GeneticVariation GWASCAT Genome-wide association study identifies multiple loci associated with bladder cancer risk. 24163127

2014
Entrez Id: 81037
Gene Symbol: CLPTM1L
CLPTM1L
CUI: C0023434
Disease: Chronic Lymphocytic Leukemia
Chronic Lymphocytic Leukemia 		0.100 GeneticVariation GWASCAT A genome-wide association study identifies multiple susceptibility loci for chronic lymphocytic leukemia. 24292274

2014
Entrez Id: 81037
Gene Symbol: CLPTM1L
CLPTM1L
CUI: C0855095
Disease: Small Lymphocytic Lymphoma
Small Lymphocytic Lymphoma 		0.100 GeneticVariation GWASCAT A genome-wide association study identifies multiple susceptibility loci for chronic lymphocytic leukemia. 24292274

2014
Entrez Id: 81037
Gene Symbol: CLPTM1L
CLPTM1L
CUI: C0007117
Disease: Basal cell carcinoma
Basal cell carcinoma 		0.100 GeneticVariation GWASCAT Germline sequence variants in TGM3 and RGS22 confer risk of basal cell carcinoma. 24403052

2014
Entrez Id: 81037
Gene Symbol: CLPTM1L
CLPTM1L
CUI: C0206710
Disease: Basal Cell Neoplasm
Basal Cell Neoplasm 		0.100 GeneticVariation GWASCAT Germline sequence variants in TGM3 and RGS22 confer risk of basal cell carcinoma. 24403052

2014
Entrez Id: 81037
Gene Symbol: CLPTM1L
CLPTM1L
CUI: C0751676
Disease: Basal Cell Cancer
Basal Cell Cancer 		0.100 GeneticVariation GWASCAT Germline sequence variants in TGM3 and RGS22 confer risk of basal cell carcinoma. 24403052

2014
Entrez Id: 81037
Gene Symbol: CLPTM1L
CLPTM1L
CUI: C0235974
Disease: Pancreatic carcinoma
Pancreatic carcinoma 		0.160 GeneticVariation GWASCAT Genome-wide association study identifies multiple susceptibility loci for pancreatic cancer. 25086665

2014
Entrez Id: 81037
Gene Symbol: CLPTM1L
CLPTM1L
CUI: C0007117
Disease: Basal cell carcinoma
Basal cell carcinoma 		0.100 GeneticVariation GWASCAT New basal cell carcinoma susceptibility loci. 25855136

2015
Entrez Id: 81037
Gene Symbol: CLPTM1L
CLPTM1L
CUI: C0206710
Disease: Basal Cell Neoplasm
Basal Cell Neoplasm 		0.100 GeneticVariation GWASCAT New basal cell carcinoma susceptibility loci. 25855136

2015
Entrez Id: 81037
Gene Symbol: CLPTM1L
CLPTM1L
CUI: C0751676
Disease: Basal Cell Cancer
Basal Cell Cancer 		0.100 GeneticVariation GWASCAT New basal cell carcinoma susceptibility loci. 25855136

2015
Entrez Id: 81037
Gene Symbol: CLPTM1L
CLPTM1L
CUI: C0235974
Disease: Pancreatic carcinoma
Pancreatic carcinoma 		0.160 GeneticVariation GWASCAT Common variation at 2p13.3, 3q29, 7p13 and 17q25.1 associated with susceptibility to pancreatic cancer. 26098869

2015
Entrez Id: 81037
Gene Symbol: CLPTM1L
CLPTM1L
CUI: C0027439
Disease: Nasopharyngeal Neoplasms
Nasopharyngeal Neoplasms 		0.100 GeneticVariation GWASCAT A GWAS Meta-analysis and Replication Study Identifies a Novel Locus within CLPTM1L/TERT Associated with Nasopharyngeal Carcinoma in Individuals of Chinese Ancestry. 26545403

2016
Entrez Id: 81037
Gene Symbol: CLPTM1L
CLPTM1L
CUI: C0027439
Disease: Nasopharyngeal Neoplasms
Nasopharyngeal Neoplasms 		0.100 GeneticVariation GWASCAT An extended genome-wide association study identifies novel susceptibility loci for nasopharyngeal carcinoma. 27436580

2016
Entrez Id: 81037
Gene Symbol: CLPTM1L
CLPTM1L
CUI: C0007117
Disease: Basal cell carcinoma
Basal cell carcinoma 		0.100 GeneticVariation GWASCAT Genome-wide association study identifies 14 novel risk alleles associated with basal cell carcinoma. 27539887

2016
Entrez Id: 81037
Gene Symbol: CLPTM1L
CLPTM1L
CUI: C0206710
Disease: Basal Cell Neoplasm
Basal Cell Neoplasm 		0.100 GeneticVariation GWASCAT Genome-wide association study identifies 14 novel risk alleles associated with basal cell carcinoma. 27539887

2016
Entrez Id: 81037
Gene Symbol: CLPTM1L
CLPTM1L
CUI: C0751676
Disease: Basal Cell Cancer
Basal Cell Cancer 		0.100 GeneticVariation GWASCAT Genome-wide association study identifies 14 novel risk alleles associated with basal cell carcinoma. 27539887

2016