Source: GWASCAT

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 149233
Gene Symbol: IL23R
IL23R
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.700 GeneticVariation GWASCAT 1000 Genomes-based imputation identifies novel and refined associations for the Wellcome Trust Case Control Consortium phase 1 Data. 22293688

2012
Entrez Id: 146
Gene Symbol: ADRA1D
ADRA1D
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.100 GeneticVariation GWASCAT LRRK2 but not ATG16L1 is associated with Paneth cell defect in Japanese Crohn's disease patients. 28352666

2017
Entrez Id: 55270
Gene Symbol: NUDT15
NUDT15
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.150 GeneticVariation GWASCAT A common missense variant in NUDT15 confers susceptibility to thiopurine-induced leukopenia. 25108385

2014
Entrez Id: 6774
Gene Symbol: STAT3
STAT3
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.500 GeneticVariation GWASCAT A genome-wide association study identifies 2 susceptibility Loci for Crohn's disease in a Japanese population. 23266558

2013
Entrez Id: 5460
Gene Symbol: POU5F1
POU5F1
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.120 GeneticVariation GWASCAT A genome-wide association study identifies 2 susceptibility Loci for Crohn's disease in a Japanese population. 23266558

2013
Entrez Id: 9873
Gene Symbol: FCHSD2
FCHSD2
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.110 GeneticVariation GWASCAT A genome-wide association study identifies 2 susceptibility Loci for Crohn's disease in a Japanese population. 23266558

2013
Entrez Id: 100130889
Gene Symbol: PSORS1C3
PSORS1C3
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.100 GeneticVariation GWASCAT A genome-wide association study identifies 2 susceptibility Loci for Crohn's disease in a Japanese population. 23266558

2013
Entrez Id: 1997
Gene Symbol: ELF1
ELF1
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.100 GeneticVariation GWASCAT A genome-wide association study identifies 2 susceptibility Loci for Crohn's disease in a Japanese population. 23266558

2013
Entrez Id: 149233
Gene Symbol: IL23R
IL23R
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.700 GeneticVariation GWASCAT A Genome-wide Association Study Identifying RAP1A as a Novel Susceptibility Gene for Crohn's Disease in Japanese Individuals. 30500874

2019
Entrez Id: 246778
Gene Symbol: IL27
IL27
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.170 GeneticVariation GWASCAT A Genome-wide Association Study Identifying RAP1A as a Novel Susceptibility Gene for Crohn's Disease in Japanese Individuals. 30500874

2019
Entrez Id: 400757
Gene Symbol: C1orf141
C1orf141
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.100 GeneticVariation GWASCAT A Genome-wide Association Study Identifying RAP1A as a Novel Susceptibility Gene for Crohn's Disease in Japanese Individuals. 30500874

2019
Entrez Id: 55924
Gene Symbol: INKA2
INKA2
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.100 GeneticVariation GWASCAT A Genome-wide Association Study Identifying RAP1A as a Novel Susceptibility Gene for Crohn's Disease in Japanese Individuals. 30500874

2019
Entrez Id: 64127
Gene Symbol: NOD2
NOD2
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		1.000 GeneticVariation GWASCAT A genome-wide association study on a southern European population identifies a new Crohn's disease susceptibility locus at RBX1-EP300. 22936669

2013
Entrez Id: 55054
Gene Symbol: ATG16L1
ATG16L1
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.700 GeneticVariation GWASCAT A genome-wide association study on a southern European population identifies a new Crohn's disease susceptibility locus at RBX1-EP300. 22936669

2013
Entrez Id: 149233
Gene Symbol: IL23R
IL23R
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.700 GeneticVariation GWASCAT A genome-wide association study on a southern European population identifies a new Crohn's disease susceptibility locus at RBX1-EP300. 22936669

2013
Entrez Id: 3460
Gene Symbol: IFNGR2
IFNGR2
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.120 GeneticVariation GWASCAT A genome-wide association study on a southern European population identifies a new Crohn's disease susceptibility locus at RBX1-EP300. 22936669

2013
Entrez Id: 677775
Gene Symbol: SCARNA5
SCARNA5
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.100 GeneticVariation GWASCAT A genome-wide association study on a southern European population identifies a new Crohn's disease susceptibility locus at RBX1-EP300. 22936669

2013
Entrez Id: 64127
Gene Symbol: NOD2
NOD2
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		1.000 GeneticVariation GWASCAT A genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibility loci. 22412388

2012
Entrez Id: 149233
Gene Symbol: IL23R
IL23R
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.700 GeneticVariation GWASCAT A genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibility loci. 22412388

2012
Entrez Id: 55054
Gene Symbol: ATG16L1
ATG16L1
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.700 GeneticVariation GWASCAT A genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibility loci. 22412388

2012
Entrez Id: 22891
Gene Symbol: ZNF365
ZNF365
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.160 GeneticVariation GWASCAT A genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibility loci. 22412388

2012
Entrez Id: 150962
Gene Symbol: PUS10
PUS10
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.110 GeneticVariation GWASCAT A genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibility loci. 22412388

2012
Entrez Id: 157869
Gene Symbol: SBSPON
SBSPON
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.100 GeneticVariation GWASCAT A genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibility loci. 22412388

2012
Entrez Id: 150962
Gene Symbol: PUS10
PUS10
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.110 GeneticVariation GWASCAT A meta-analysis of genome-wide association scans identifies IL18RAP, PTPN2, TAGAP, and PUS10 as shared risk loci for Crohn's disease and celiac disease. 21298027

2011
Entrez Id: 64127
Gene Symbol: NOD2
NOD2
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		1.000 GeneticVariation GWASCAT A proportion of these were replicated in two independent German Caucasian samples, including the established CD loci NOD2 and IBD5. 17804789

2007