colitis Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An inflammatory bowel disease that involves inflammation located_in colon. (Human Disease Ontology, DOID_0060180)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0002583
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Genes

12 genes associated with the colitis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
CIITA class II, major histocompatibility complex, transactivator
GPIHBP1 glycosylphosphatidylinositol anchored high density lipoprotein binding protein 1
IGHM immunoglobulin heavy constant mu
IL10RA interleukin 10 receptor, alpha
IL10RB interleukin 10 receptor, beta
LRBA LPS-responsive vesicle trafficking, beach and anchor containing
OPLAH 5-oxoprolinase (ATP-hydrolysing)
PLCG2 phospholipase C, gamma 2 (phosphatidylinositol-specific)
RFX5 regulatory factor X, 5 (influences HLA class II expression)
RFXANK regulatory factor X-associated ankyrin-containing protein
RFXAP regulatory factor X-associated protein
SKIV2L superkiller viralicidic activity 2-like (S. cerevisiae)