Colitis Gene Set

Dataset HuGE Navigator Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description An inflammatory bowel disease that involves inflammation located_in colon. (Human Disease Ontology, DOID_0060180)
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Genes

21 genes associated with the Colitis phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Symbol Name
APC adenomatous polyposis coli
ATG16L1 autophagy related 16-like 1 (S. cerevisiae)
BPI bactericidal/permeability-increasing protein
C5ORF56 chromosome 5 open reading frame 56
F5 coagulation factor V (proaccelerin, labile factor)
FAAH fatty acid amide hydrolase
HP haptoglobin
HPS1 Hermansky-Pudlak syndrome 1
HPS4 Hermansky-Pudlak syndrome 4
IL23R interleukin 23 receptor
IRGM immunity-related GTPase family, M
JAK2 Janus kinase 2
LACC1 laccase (multicopper oxidoreductase) domain containing 1
MOK MOK protein kinase
NOD2 nucleotide-binding oligomerization domain containing 2
PRDM1 PR domain containing 1, with ZNF domain
PTGER4 prostaglandin E receptor 4 (subtype EP4)
STAT5A signal transducer and activator of transcription 5A
TNFRSF1A tumor necrosis factor receptor superfamily, member 1A
TNFRSF1B tumor necrosis factor receptor superfamily, member 1B
TNFSF15 tumor necrosis factor (ligand) superfamily, member 15