Source: GWASCAT

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 7148
Gene Symbol: TNXB
TNXB
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.430 GeneticVariation GWASCAT Genome-Wide Association Study Detected Novel Susceptibility Genes for Schizophrenia and Shared Trans-Populations/Diseases Genetic Effect. 30285260

2019
Entrez Id: 7148
Gene Symbol: TNXB
TNXB
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.430 GeneticVariation GWASCAT Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia. 28540026

2017
Entrez Id: 7148
Gene Symbol: TNXB
TNXB
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		0.130 GeneticVariation GWASCAT Transancestral mapping and genetic load in systemic lupus erythematosus. 28714469

2017
Entrez Id: 7148
Gene Symbol: TNXB
TNXB
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		0.130 GeneticVariation GWASCAT Identification of a New Susceptibility Locus for Systemic Lupus Erythematosus on Chromosome 12 in Individuals of European Ancestry. 26316170

2016
Entrez Id: 7148
Gene Symbol: TNXB
TNXB
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		0.130 GeneticVariation GWASCAT Genome-wide association meta-analysis in Chinese and European individuals identifies ten new loci associated with systemic lupus erythematosus. 27399966

2016
Entrez Id: 7148
Gene Symbol: TNXB
TNXB
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		0.130 GeneticVariation GWASCAT Genetic association analyses implicate aberrant regulation of innate and adaptive immunity genes in the pathogenesis of systemic lupus erythematosus. 26502338

2015
Entrez Id: 7148
Gene Symbol: TNXB
TNXB
CUI: C0242383
Disease: Age related macular degeneration
Age related macular degeneration 		0.130 GeneticVariation GWASCAT Genome-wide association study of age-related macular degeneration identifies associated variants in the TNXB-FKBPL-NOTCH4 region of chromosome 6p21.3. 22694956

2012
Entrez Id: 7148
Gene Symbol: TNXB
TNXB
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		0.130 GeneticVariation GWASCAT Differential genetic associations for systemic lupus erythematosus based on anti-dsDNA autoantibody production. 21408207

2011
Entrez Id: 7148
Gene Symbol: TNXB
TNXB
CUI: C0003872
Disease: Arthritis, Psoriatic
Arthritis, Psoriatic 		0.100 GeneticVariation GWASCAT Genetic variation at the glycosaminoglycan metabolism pathway contributes to the risk of psoriatic arthritis but not psoriasis. 30552173

2019
Entrez Id: 7148
Gene Symbol: TNXB
TNXB
CUI: C0149745
Disease: Oral Ulcer
Oral Ulcer 		0.100 GeneticVariation GWASCAT Genome wide analysis for mouth ulcers identifies associations at immune regulatory loci. 30837455

2019
Entrez Id: 7148
Gene Symbol: TNXB
TNXB
CUI: C0027873
Disease: Neuromyelitis Optica
Neuromyelitis Optica 		0.100 GeneticVariation GWASCAT A whole-genome sequence study identifies genetic risk factors for neuromyelitis optica. 29769526

2018
Entrez Id: 7148
Gene Symbol: TNXB
TNXB
CUI: C0040420
Disease: Tonometry
Tonometry 		0.100 GeneticVariation GWASCAT Genome-wide association analyses identify new loci influencing intraocular pressure. 29617998

2018
Entrez Id: 7148
Gene Symbol: TNXB
TNXB
CUI: C0040420
Disease: Tonometry
Tonometry 		0.100 GeneticVariation GWASCAT Genome-wide association study of intraocular pressure uncovers new pathways to glaucoma. 30054594

2018
Entrez Id: 7148
Gene Symbol: TNXB
TNXB
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.100 GeneticVariation GWASCAT Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals. 30038396

2018
Entrez Id: 7148
Gene Symbol: TNXB
TNXB
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.100 GeneticVariation GWASCAT Genomic atlas of the human plasma proteome. 29875488

2018
Entrez Id: 7148
Gene Symbol: TNXB
TNXB
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.100 GeneticVariation GWASCAT Co-regulatory networks of human serum proteins link genetics to disease. 30072576

2018
Entrez Id: 7148
Gene Symbol: TNXB
TNXB
CUI: C0008074
Disease: Child Development Disorders, Pervasive
Child Development Disorders, Pervasive 		0.100 GeneticVariation GWASCAT Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia. 28540026

2017
Entrez Id: 7148
Gene Symbol: TNXB
TNXB
CUI: C0149782
Disease: Squamous cell carcinoma of lung
Squamous cell carcinoma of lung 		0.100 GeneticVariation GWASCAT Large-scale association analysis identifies new lung cancer susceptibility loci and heterogeneity in genetic susceptibility across histological subtypes. 28604730

2017
Entrez Id: 7148
Gene Symbol: TNXB
TNXB
CUI: C0577608
Disease: C4 complement assay (procedure)
C4 complement assay (procedure) 		0.100 GeneticVariation GWASCAT Connecting genetic risk to disease end points through the human blood plasma proteome. 28240269

2017
Entrez Id: 7148
Gene Symbol: TNXB
TNXB
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung 		0.100 GeneticVariation GWASCAT Large-scale association analysis identifies new lung cancer susceptibility loci and heterogeneity in genetic susceptibility across histological subtypes. 28604730

2017
Entrez Id: 7148
Gene Symbol: TNXB
TNXB
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.100 GeneticVariation GWASCAT Novel Blood Pressure Locus and Gene Discovery Using Genome-Wide Association Study and Expression Data Sets From Blood and the Kidney. 28739976

2017
Entrez Id: 7148
Gene Symbol: TNXB
TNXB
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.100 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252

2016
Entrez Id: 7148
Gene Symbol: TNXB
TNXB
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.100 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252

2016
Entrez Id: 7148
Gene Symbol: TNXB
TNXB
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test) 		0.100 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252

2016
Entrez Id: 7148
Gene Symbol: TNXB
TNXB
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result) 		0.100 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252

2016