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: C0007131
Disease: Non-Small Cell Lung Carcinoma
Non-Small Cell Lung Carcinoma 		0.470 GeneticVariation GWASCAT Identification of risk loci and a polygenic risk score for lung cancer: a large-scale prospective cohort study in Chinese populations. 31326317

2019
Entrez Id: 81037
Gene Symbol: CLPTM1L
CLPTM1L
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
Adenocarcinoma of lung (disorder) 		0.460 GeneticVariation GWASCAT Identification of risk loci and a polygenic risk score for lung cancer: a large-scale prospective cohort study in Chinese populations. 31326317

2019
Entrez Id: 81037
Gene Symbol: CLPTM1L
CLPTM1L
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
Adenocarcinoma of lung (disorder) 		0.460 GeneticVariation GWASCAT Lung Cancer Risk in Never-Smokers of European Descent is Associated With Genetic Variation in the 5p15.33 TERT-CLPTM1Ll Region. 31009812

2019
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: C0153381
Disease: Malignant neoplasm of mouth
Malignant neoplasm of mouth 		0.410 GeneticVariation GWASCAT Oral cancer was associated with two new regions, 2p23.3 (rs6547741, GPN1) and 9q34.12 (rs928674, LAMC3), and with known cancer-related loci-9p21.3 (rs8181047, CDKN2B-AS1) and 5p15.33 (rs10462706, CLPTM1L). 27749845

2016
Entrez Id: 81037
Gene Symbol: CLPTM1L
CLPTM1L
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung 		0.200 GeneticVariation GWASCAT Lung Cancer Risk in Never-Smokers of European Descent is Associated With Genetic Variation in the 5p15.33 TERT-CLPTM1Ll Region. 31009812

2019
Entrez Id: 81037
Gene Symbol: CLPTM1L
CLPTM1L
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung 		0.200 GeneticVariation GWASCAT Large-scale association analysis identifies new lung cancer susceptibility loci and heterogeneity in genetic susceptibility across histological subtypes. 28604730

2017
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: C0235974
Disease: Pancreatic carcinoma
Pancreatic carcinoma 		0.160 GeneticVariation GWASCAT Genome-wide meta-analysis identifies five new susceptibility loci for pancreatic cancer. 29422604

2018
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: 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: 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: 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: C0149782
Disease: Squamous cell carcinoma of lung
Squamous cell carcinoma of lung 		0.110 GeneticVariation GWASCAT Large-scale association analysis identifies new lung cancer susceptibility loci and heterogeneity in genetic susceptibility across histological subtypes. 28604730

2017
Entrez Id: 81037
Gene Symbol: CLPTM1L
CLPTM1L
CUI: C0220633
Disease: Uveal melanoma
Uveal melanoma 		0.110 GeneticVariation GWASCAT A GWAS in uveal melanoma identifies risk polymorphisms in the CLPTM1L locus. 28781888

2017
Entrez Id: 81037
Gene Symbol: CLPTM1L
CLPTM1L
CUI: C0007117
Disease: Basal cell carcinoma
Basal cell carcinoma 		0.100 GeneticVariation GWASCAT Combined analysis of keratinocyte cancers identifies novel genome-wide loci. 31174203

2019
Entrez Id: 81037
Gene Symbol: CLPTM1L
CLPTM1L
CUI: C0206710
Disease: Basal Cell Neoplasm
Basal Cell Neoplasm 		0.100 GeneticVariation GWASCAT Combined analysis of keratinocyte cancers identifies novel genome-wide loci. 31174203

2019
Entrez Id: 81037
Gene Symbol: CLPTM1L
CLPTM1L
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.100 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370

2019
Entrez Id: 81037
Gene Symbol: CLPTM1L
CLPTM1L
CUI: C0751676
Disease: Basal Cell Cancer
Basal Cell Cancer 		0.100 GeneticVariation GWASCAT Combined analysis of keratinocyte cancers identifies novel genome-wide loci. 31174203

2019
Entrez Id: 81037
Gene Symbol: CLPTM1L
CLPTM1L
CUI: C1304746
Disease: RDW - Red blood cell distribution width result
RDW - Red blood cell distribution width result 		0.100 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370

2019
Entrez Id: 81037
Gene Symbol: CLPTM1L
CLPTM1L
CUI: C0151779
Disease: Cutaneous Melanoma
Cutaneous Melanoma 		0.100 GeneticVariation GWASCAT Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways. 30429480

2018
Entrez Id: 81037
Gene Symbol: CLPTM1L
CLPTM1L
CUI: C0153535
Disease: Malignant melanoma of skin of upper limb
Malignant melanoma of skin of upper limb 		0.100 GeneticVariation GWASCAT Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways. 30429480

2018
Entrez Id: 81037
Gene Symbol: CLPTM1L
CLPTM1L
CUI: C0153536
Disease: Malignant melanoma of skin of lower limb
Malignant melanoma of skin of lower limb 		0.100 GeneticVariation GWASCAT Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways. 30429480

2018
Entrez Id: 81037
Gene Symbol: CLPTM1L
CLPTM1L
CUI: C0201544
Disease: Prostate specific antigen measurement
Prostate specific antigen measurement 		0.100 GeneticVariation GWASCAT Genome-wide associations for benign prostatic hyperplasia reveal a genetic correlation with serum levels of PSA. 30410027

2018
Entrez Id: 81037
Gene Symbol: CLPTM1L
CLPTM1L
CUI: C0574785
Disease: Lower Urinary Tract Symptoms
Lower Urinary Tract Symptoms 		0.100 GeneticVariation GWASCAT Genome-wide associations for benign prostatic hyperplasia reveal a genetic correlation with serum levels of PSA. 30410027

2018