crohn disease Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description An intestinal disease that involves inflammation located_in intestine. (Human Disease Ontology, DOID_8778)
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66 genes associated with the disease crohn disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
ABCB1 ATP-binding cassette, sub-family B (MDR/TAP), member 1
ATG16L1 autophagy related 16-like 1 (S. cerevisiae)
BACH2 BTB and CNC homology 1, basic leucine zipper transcription factor 2
BSN bassoon presynaptic cytomatrix protein
C5ORF56 chromosome 5 open reading frame 56
CARD9 caspase recruitment domain family, member 9
CASP9 caspase 9, apoptosis-related cysteine peptidase
CCL2 chemokine (C-C motif) ligand 2
CDKAL1 CDK5 regulatory subunit associated protein 1-like 1
CLN3 ceroid-lipofuscinosis, neuronal 3
DEFB1 defensin, beta 1
DENND1B DENN/MADD domain containing 1B
DLG5 discs, large homolog 5 (Drosophila)
DNMT3A DNA (cytosine-5-)-methyltransferase 3 alpha
ERAP2 endoplasmic reticulum aminopeptidase 2
FASLG Fas ligand (TNF superfamily, member 6)
FCGR3A Fc fragment of IgG, low affinity IIIa, receptor (CD16a)
FGFR1OP FGFR1 oncogene partner
FUT2 fucosyltransferase 2 (secretor status included)
GCKR glucokinase (hexokinase 4) regulator
GPR65 G protein-coupled receptor 65
IBD5 inflammatory bowel disease 5
IGHG1 immunoglobulin heavy constant gamma 1 (G1m marker)
IL10 interleukin 10
IL18RAP interleukin 18 receptor accessory protein
IL23R interleukin 23 receptor
IL2RA interleukin 2 receptor, alpha
IL6 interleukin 6
ITLN1 intelectin 1 (galactofuranose binding)
LACC1 laccase (multicopper oxidoreductase) domain containing 1
MST1 macrophage stimulating 1
MTHFR methylenetetrahydrofolate reductase (NAD(P)H)
MTR 5-methyltetrahydrofolate-homocysteine methyltransferase
MTRR 5-methyltetrahydrofolate-homocysteine methyltransferase reductase
MYO9B myosin IXB
NELL1 NEL-like 1 (chicken)
NKAP NFKB activating protein
NKX2-3 NK2 homeobox 3
NOD1 nucleotide-binding oligomerization domain containing 1
NOD2 nucleotide-binding oligomerization domain containing 2
NR3C1 nuclear receptor subfamily 3, group C, member 1 (glucocorticoid receptor)
PER3 period circadian clock 3
PLCL1 phospholipase C-like 1
PPARG peroxisome proliferator-activated receptor gamma
PSMB10 proteasome (prosome, macropain) subunit, beta type, 10
PTPN22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid)
PUS10 pseudouridylate synthase 10
SBSPON somatomedin B and thrombospondin, type 1 domain containing
SCAMP3 secretory carrier membrane protein 3
SLC22A23 solute carrier family 22, member 23
SLC22A4 solute carrier family 22 (organic cation/zwitterion transporter), member 4
SLC22A5 solute carrier family 22 (organic cation/carnitine transporter), member 5
SMAD3 SMAD family member 3
SP140 SP140 nuclear body protein
STAT3 signal transducer and activator of transcription 3 (acute-phase response factor)
THADA thyroid adenoma associated
TMEM258 transmembrane protein 258
TNF tumor necrosis factor
TNFRSF1A tumor necrosis factor receptor superfamily, member 1A
TNFRSF1B tumor necrosis factor receptor superfamily, member 1B
TNFSF15 tumor necrosis factor (ligand) superfamily, member 15
TYK2 tyrosine kinase 2
UBE2L3 ubiquitin-conjugating enzyme E2L 3
ZGPAT zinc finger, CCCH-type with G patch domain
ZMIZ1 zinc finger, MIZ-type containing 1
ZNF365 zinc finger protein 365