Source: GWASDB

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 56244
Gene Symbol: BTNL2
BTNL2
CUI: C0036202
Disease: Sarcoidosis
Sarcoidosis
0.700 GeneticVariation GWASDB Genome-wide association analysis reveals 12q13.3-q14.1 as new risk locus for sarcoidosis. 22936702

2013

Entrez Id: 56244
Gene Symbol: BTNL2
BTNL2
CUI: C0036202
Disease: Sarcoidosis
Sarcoidosis
0.700 GeneticVariation GWASDB Genome-wide association study of African and European Americans implicates multiple shared and ethnic specific loci in sarcoidosis susceptibility. 22952805

2012

Entrez Id: 56244
Gene Symbol: BTNL2
BTNL2
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.120 GeneticVariation GWASDB Genome-wide association study of Crohn's disease in Koreans revealed three new susceptibility loci and common attributes of genetic susceptibility across ethnic populations. 23850713

2014

Entrez Id: 56244
Gene Symbol: BTNL2
BTNL2
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
Adenocarcinoma of lung (disorder)
0.120 GeneticVariation GWASDB A genome-wide association study identifies two new susceptibility loci for lung adenocarcinoma in the Japanese population. 22797724

2012

Entrez Id: 56244
Gene Symbol: BTNL2
BTNL2
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.120 GeneticVariation GWASDB A genome-wide association study suggests contrasting associations in ACPA-positive versus ACPA-negative rheumatoid arthritis. 21156761

2011

Entrez Id: 56244
Gene Symbol: BTNL2
BTNL2
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.120 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: 56244
Gene Symbol: BTNL2
BTNL2
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.120 GeneticVariation GWASDB Genomic DNA pooling for whole-genome association scans in complex disease: empirical demonstration of efficacy in rheumatoid arthritis. 17159887

2007

Entrez Id: 56244
Gene Symbol: BTNL2
BTNL2
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.120 GeneticVariation GWASDB TRAF1-C5 as a risk locus for rheumatoid arthritis--a genomewide study. 17804836

2007

Entrez Id: 56244
Gene Symbol: BTNL2
BTNL2
Diabetes Mellitus, Insulin-Dependent
0.120 GeneticVariation GWASDB A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene. 17632545

2007

Entrez Id: 56244
Gene Symbol: BTNL2
BTNL2
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic
0.110 GeneticVariation GWASDB GWAS identifies novel SLE susceptibility genes and explains the association of the HLA region. 24871463

2014

Entrez Id: 56244
Gene Symbol: BTNL2
BTNL2
CUI: C0338451
Disease: Frontotemporal dementia
Frontotemporal dementia
0.110 GeneticVariation GWASDB Frontotemporal dementia and its subtypes: a genome-wide association study. 24943344

2014

Entrez Id: 56244
Gene Symbol: BTNL2
BTNL2
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
0.110 GeneticVariation GWASDB Oligoclonal band status in Scandinavian multiple sclerosis patients is associated with specific genetic risk alleles. 23472185

2013

Entrez Id: 56244
Gene Symbol: BTNL2
BTNL2
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.110 GeneticVariation GWASDB Genome-wide association analyses identify 13 new susceptibility loci for generalized vitiligo. 22561518

2012

Entrez Id: 56244
Gene Symbol: BTNL2
BTNL2
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.110 GeneticVariation GWASDB Genome-wide analysis identifies a quantitative trait locus in the MHC class II region associated with generalized vitiligo age of onset. 21326295

2011

Entrez Id: 56244
Gene Symbol: BTNL2
BTNL2
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.110 GeneticVariation GWASDB Variant of TYR and autoimmunity susceptibility loci in generalized vitiligo. 20410501

2010

Entrez Id: 56244
Gene Symbol: BTNL2
BTNL2
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
0.110 GeneticVariation GWASDB Risk alleles for multiple sclerosis identified by a genomewide study. 17660530

2007

Entrez Id: 56244
Gene Symbol: BTNL2
BTNL2
CUI: C0149678
Disease: Epstein-Barr Virus Infections
Epstein-Barr Virus Infections
0.100 GeneticVariation GWASDB A genome-wide integrative genomic study localizes genetic factors influencing antibodies against Epstein-Barr virus nuclear antigen 1 (EBNA-1). 23326239

2013

Entrez Id: 56244
Gene Symbol: BTNL2
BTNL2
CUI: C0206062
Disease: Lung Diseases, Interstitial
Lung Diseases, Interstitial
0.100 GeneticVariation GWASDB Genome-wide association study identifies multiple susceptibility loci for pulmonary fibrosis. 23583980

2013

Entrez Id: 56244
Gene Symbol: BTNL2
BTNL2
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction
0.100 GeneticVariation GWASDB A genome-wide association meta-analysis of self-reported allergy identifies shared and allergy-specific susceptibility loci. 23817569

2013

Entrez Id: 56244
Gene Symbol: BTNL2
BTNL2
CUI: C0026896
Disease: Myasthenia Gravis
Myasthenia Gravis
0.100 GeneticVariation GWASDB Risk for myasthenia gravis maps to a (151) Pro→Ala change in TNIP1 and to human leukocyte antigen-B*08. 23055271

2012

Entrez Id: 56244
Gene Symbol: BTNL2
BTNL2
CUI: C4021107
Disease: Non-obstructive azoospermia
Non-obstructive azoospermia
0.100 GeneticVariation GWASDB A genome-wide association study reveals that variants within the HLA region are associated with risk for nonobstructive azoospermia. 22541561

2012

Entrez Id: 56244
Gene Symbol: BTNL2
BTNL2
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio
0.100 GeneticVariation GWASDB Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution. 20935629

2010

Entrez Id: 56244
Gene Symbol: BTNL2
BTNL2
CUI: C0409959
Disease: Osteoarthritis, Knee
Osteoarthritis, Knee
0.100 GeneticVariation GWASDB New sequence variants in HLA class II/III region associated with susceptibility to knee osteoarthritis identified by genome-wide association study. 20305777

2010

Entrez Id: 56244
Gene Symbol: BTNL2
BTNL2
CUI: C0027404
Disease: Narcolepsy
Narcolepsy
0.100 GeneticVariation GWASDB Genome-wide association database developed in the Japanese Integrated Database Project. 19629137

2009

Entrez Id: 56244
Gene Symbol: BTNL2
BTNL2
Anti-cyclic citrullinated peptide antibody
0.100 GeneticVariation GWASDB Genome-wide association study of determinants of anti-cyclic citrullinated peptide antibody titer in adults with rheumatoid arthritis. 19287509

2009