Source: GWASDB

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 7148
Gene Symbol: TNXB
TNXB
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		0.130 GeneticVariation GWASDB GWAS identifies novel SLE susceptibility genes and explains the association of the HLA region. 24871463

2014
Entrez Id: 7148
Gene Symbol: TNXB
TNXB
CUI: C0242383
Disease: Age related macular degeneration
Age related macular degeneration 		0.130 GeneticVariation GWASDB 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 GWASDB Differential genetic associations for systemic lupus erythematosus based on anti-dsDNA autoantibody production. 21408207

2011
Entrez Id: 7148
Gene Symbol: TNXB
TNXB
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		0.130 GeneticVariation GWASDB Our findings strongly imply that the TNXB gene is a candidate gene susceptible to SLE in the Japanese population. 18058064

2008
Entrez Id: 7148
Gene Symbol: TNXB
TNXB
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.110 GeneticVariation GWASDB A genome-wide association study suggests contrasting associations in ACPA-positive versus ACPA-negative rheumatoid arthritis. 21156761

2011
Entrez Id: 7148
Gene Symbol: TNXB
TNXB
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.110 GeneticVariation GWASDB REL, encoding a member of the NF-kappaB family of transcription factors, is a newly defined risk locus for rheumatoid arthritis. 19503088

2009
Entrez Id: 7148
Gene Symbol: TNXB
TNXB
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.110 GeneticVariation GWASDB TRAF1-C5 as a risk locus for rheumatoid arthritis--a genomewide study. 17804836

2007
Entrez Id: 7148
Gene Symbol: TNXB
TNXB
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
Diabetes Mellitus, Insulin-Dependent 		0.110 GeneticVariation GWASDB A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene. 17632545

2007
Entrez Id: 7148
Gene Symbol: TNXB
TNXB
CUI: C0011615
Disease: Dermatitis, Atopic
Dermatitis, Atopic 		0.100 GeneticVariation GWASDB A genome-wide association study of atopic dermatitis identifies loci with overlapping effects on asthma and psoriasis. 23886662

2013
Entrez Id: 7148
Gene Symbol: TNXB
TNXB
CUI: C0577608
Disease: C4 complement assay (procedure)
C4 complement assay (procedure) 		0.100 GeneticVariation GWASDB Genome-wide association study for serum complement C3 and C4 levels in healthy Chinese subjects. 23028341

2012
Entrez Id: 7148
Gene Symbol: TNXB
TNXB
CUI: C0005823
Disease: Blood Pressure
Blood Pressure 		0.100 GeneticVariation GWASDB Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure. 21909110

2011
Entrez Id: 7148
Gene Symbol: TNXB
TNXB
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement 		0.100 GeneticVariation GWASDB Genetic loci associated with plasma phospholipid n-3 fatty acids: a meta-analysis of genome-wide association studies from the CHARGE Consortium. 21829377

2011
Entrez Id: 7148
Gene Symbol: TNXB
TNXB
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		0.100 GeneticVariation GWASDB Genetic predictors of medically refractory ulcerative colitis. 20848476

2010
Entrez Id: 7148
Gene Symbol: TNXB
TNXB
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.100 GeneticVariation GWASDB Evidence for VAV2 and ZNF433 as susceptibility genes for multiple sclerosis. 20598377

2010
Entrez Id: 7148
Gene Symbol: TNXB
TNXB
CUI: C0036421
Disease: Systemic Scleroderma
Systemic Scleroderma 		0.100 GeneticVariation GWASDB Genome-wide association study of systemic sclerosis identifies CD247 as a new susceptibility locus. 20383147

2010
Entrez Id: 7148
Gene Symbol: TNXB
TNXB
CUI: C0042900
Disease: Vitiligo
Vitiligo 		0.100 GeneticVariation GWASDB Genome-wide association study for vitiligo identifies susceptibility loci at 6q27 and the MHC. 20526339

2010
Entrez Id: 7148
Gene Symbol: TNXB
TNXB
CUI: C1836230
Disease: HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO
HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO 		0.100 GeneticVariation GWASDB The major genetic determinants of HIV-1 control affect HLA class I peptide presentation. 21051598

2010
Entrez Id: 7148
Gene Symbol: TNXB
TNXB
CUI: C1836231
Disease: HIV-1, RESISTANCE TO
HIV-1, RESISTANCE TO 		0.100 GeneticVariation GWASDB The major genetic determinants of HIV-1 control affect HLA class I peptide presentation. 21051598

2010
Entrez Id: 7148
Gene Symbol: TNXB
TNXB
CUI: C1836232
Disease: ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO
ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO 		0.100 GeneticVariation GWASDB The major genetic determinants of HIV-1 control affect HLA class I peptide presentation. 21051598

2010
Entrez Id: 7148
Gene Symbol: TNXB
TNXB
CUI: C1836233
Disease: AIDS, PROGRESSION TO
AIDS, PROGRESSION TO 		0.100 GeneticVariation GWASDB The major genetic determinants of HIV-1 control affect HLA class I peptide presentation. 21051598

2010
Entrez Id: 7148
Gene Symbol: TNXB
TNXB
CUI: C0001175
Disease: Acquired Immunodeficiency Syndrome
Acquired Immunodeficiency Syndrome 		0.100 GeneticVariation GWASDB Genomewide association study of an AIDS-nonprogression cohort emphasizes the role played by HLA genes (ANRS Genomewide Association Study 02). 19115949

2009
Entrez Id: 7148
Gene Symbol: TNXB
TNXB
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
Adenocarcinoma of lung (disorder) 		0.100 GeneticVariation GWASDB A genome-wide association study of lung cancer identifies a region of chromosome 5p15 associated with risk for adenocarcinoma. 19836008

2009
Entrez Id: 7148
Gene Symbol: TNXB
TNXB
CUI: C1836230
Disease: HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO
HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO 		0.100 GeneticVariation GWASDB Common genetic variation and the control of HIV-1 in humans. 20041166

2009
Entrez Id: 7148
Gene Symbol: TNXB
TNXB
CUI: C1836231
Disease: HIV-1, RESISTANCE TO
HIV-1, RESISTANCE TO 		0.100 GeneticVariation GWASDB Common genetic variation and the control of HIV-1 in humans. 20041166

2009
Entrez Id: 7148
Gene Symbol: TNXB
TNXB
CUI: C1836232
Disease: ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO
ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO 		0.100 GeneticVariation GWASDB Common genetic variation and the control of HIV-1 in humans. 20041166

2009