Source: GWASDB

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4855
Gene Symbol: NOTCH4
NOTCH4
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.500 GeneticVariation GWASDB A comprehensive family-based replication study of schizophrenia genes. 23894747

2013

Entrez Id: 4855
Gene Symbol: NOTCH4
NOTCH4
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.500 GeneticVariation GWASDB Common variants at VRK2 and TCF4 conferring risk of schizophrenia. 21791550

2011

Entrez Id: 4855
Gene Symbol: NOTCH4
NOTCH4
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.500 GeneticVariation GWASDB Common variants conferring risk of schizophrenia. 19571808

2009

Entrez Id: 4855
Gene Symbol: NOTCH4
NOTCH4
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.150 GeneticVariation GWASDB A genome-wide association study suggests contrasting associations in ACPA-positive versus ACPA-negative rheumatoid arthritis. 21156761

2011

Entrez Id: 4855
Gene Symbol: NOTCH4
NOTCH4
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.150 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: 4855
Gene Symbol: NOTCH4
NOTCH4
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.150 GeneticVariation GWASDB TRAF1-C5 as a risk locus for rheumatoid arthritis--a genomewide study. 17804836

2007

Entrez Id: 4855
Gene Symbol: NOTCH4
NOTCH4
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
0.130 GeneticVariation GWASDB Evidence for VAV2 and ZNF433 as susceptibility genes for multiple sclerosis. 20598377

2010

Entrez Id: 4855
Gene Symbol: NOTCH4
NOTCH4
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
0.130 GeneticVariation GWASDB Risk alleles for multiple sclerosis identified by a genomewide study. 17660530

2007

Entrez Id: 4855
Gene Symbol: NOTCH4
NOTCH4
CUI: C0036421
Disease: Systemic Scleroderma
Systemic Scleroderma
0.120 GeneticVariation GWASDB Identification of novel genetic markers associated with clinical phenotypes of systemic sclerosis through a genome-wide association strategy. 21779181

2011

Entrez Id: 4855
Gene Symbol: NOTCH4
NOTCH4
CUI: C0036421
Disease: Systemic Scleroderma
Systemic Scleroderma
0.120 GeneticVariation GWASDB Genome-wide association study of systemic sclerosis identifies CD247 as a new susceptibility locus. 20383147

2010

Entrez Id: 4855
Gene Symbol: NOTCH4
NOTCH4
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: 4855
Gene Symbol: NOTCH4
NOTCH4
CUI: C0242383
Disease: Age related macular degeneration
Age related macular degeneration
0.110 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: 4855
Gene Symbol: NOTCH4
NOTCH4
CUI: C0004096
Disease: Asthma
Asthma
0.110 GeneticVariation GWASDB Genome-wide association study identifies three new susceptibility loci for adult asthma in the Japanese population. 21804548

2011

Entrez Id: 4855
Gene Symbol: NOTCH4
NOTCH4
CUI: C0027404
Disease: Narcolepsy
Narcolepsy
0.110 GeneticVariation GWASDB Genome-wide association database developed in the Japanese Integrated Database Project. 19629137

2009

Entrez Id: 4855
Gene Symbol: NOTCH4
NOTCH4
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
Adenocarcinoma of lung (disorder)
0.110 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: 4855
Gene Symbol: NOTCH4
NOTCH4
CUI: C2698399
Disease: Myeloperoxidase Measurement
Myeloperoxidase Measurement
0.100 GeneticVariation GWASDB Genome-wide and gene-centric analyses of circulating myeloperoxidase levels in the charge and care consortia. 23620142

2013

Entrez Id: 4855
Gene Symbol: NOTCH4
NOTCH4
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: 4855
Gene Symbol: NOTCH4
NOTCH4
CUI: C0030809
Disease: Pemphigus Vulgaris
Pemphigus Vulgaris
0.100 GeneticVariation GWASDB Population-specific association between a polymorphic variant in ST18, encoding a pro-apoptotic molecule, and pemphigus vulgaris. 22437316

2012

Entrez Id: 4855
Gene Symbol: NOTCH4
NOTCH4
CUI: C0036202
Disease: Sarcoidosis
Sarcoidosis
0.100 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: 4855
Gene Symbol: NOTCH4
NOTCH4
CUI: C0162701
Disease: Polysomnography
Polysomnography
0.100 GeneticVariation GWASDB Novel genetic loci identified for the pathophysiology of childhood obesity in the Hispanic population. 23251661

2012

Entrez Id: 4855
Gene Symbol: NOTCH4
NOTCH4
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung
0.100 GeneticVariation GWASDB Influence of common genetic variation on lung cancer risk: meta-analysis of 14 900 cases and 29 485 controls. 22899653

2012

Entrez Id: 4855
Gene Symbol: NOTCH4
NOTCH4
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: 4855
Gene Symbol: NOTCH4
NOTCH4
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: 4855
Gene Symbol: NOTCH4
NOTCH4
CUI: C0231921
Disease: Pulmonary function
Pulmonary function
0.100 GeneticVariation GWASDB Meta-analyses of genome-wide association studies identify multiple loci associated with pulmonary function. 20010835

2010

Entrez Id: 4855
Gene Symbol: NOTCH4
NOTCH4
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