Crohn Disease Gene Set

Dataset dbGAP Gene-Trait Associations
Category disease or phenotype associations
Type trait
Description An intestinal disease that involves inflammation located_in intestine. (Human Disease Ontology, DOID_8778)
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Genes

20 genes associated with the trait Crohn Disease in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

Symbol Name Standardized Value
IL23R interleukin 23 receptor 2.01467
NOD2 nucleotide-binding oligomerization domain containing 2 1.78203
ATG16L1 autophagy related 16-like 1 (S. cerevisiae) 1.71516
C5ORF56 chromosome 5 open reading frame 56 1.33728
NKX2-3 NK2 homeobox 3 1.25845
LACC1 laccase (multicopper oxidoreductase) domain containing 1 1.11353
FGFR1OP FGFR1 oncogene partner 1.07287
MST1 macrophage stimulating 1 1.07287
STAT3 signal transducer and activator of transcription 3 (acute-phase response factor) 1.02473
TNFSF15 tumor necrosis factor (ligand) superfamily, member 15 0.907793
CDKAL1 CDK5 regulatory subunit associated protein 1-like 1 0.866561
ITLN1 intelectin 1 (galactofuranose binding) 0.862644
PUS10 pseudouridylate synthase 10 0.796965
ZNF365 zinc finger protein 365 0.781064
PTPN22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid) 0.763999
FUT2 fucosyltransferase 2 (secretor status included) 0.731179
SBSPON somatomedin B and thrombospondin, type 1 domain containing 0.731179
BSN bassoon presynaptic cytomatrix protein 0.696869
PSMB10 proteasome (prosome, macropain) subunit, beta type, 10 0.609816
NELL1 NEL-like 1 (chicken) 0.406869