Gastroenteritis Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A gastrointestinal system infectious disease that involves inflammation of the lining of the stomach and small and large intestines, which is caused by viruses, bacteria, or parasites. Chemicals and drugs also cause gastroenteritis. The symptoms include diarrhea, loss of appetite, nausea, vomiting, cramps, and discomfort in the abdomen. (Human Disease Ontology, DOID_2326)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D005759
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Genes

16 genes/proteins associated with the disease Gastroenteritis from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
F2RL1 coagulation factor II (thrombin) receptor-like 1 2.88009
MPO myeloperoxidase 1.20328
IFNG interferon, gamma 1.18816
IL6 interleukin 6 1.16104
CXCL8 chemokine (C-X-C motif) ligand 8 1.16104
CAT catalase 1.11673
NOS2 nitric oxide synthase 2, inducible 1.10907
NFKBIA nuclear factor of kappa light polypeptide gene enhancer in B-cells inhibitor, alpha 1.09822
EGR1 early growth response 1 1.06116
IL2 interleukin 2 1.05535
IL1B interleukin 1, beta 1.05274
MAPK3 mitogen-activated protein kinase 3 1.03567
CDKN1A cyclin-dependent kinase inhibitor 1A (p21, Cip1) 1.03159
MAPK1 mitogen-activated protein kinase 1 1.02821
IL4 interleukin 4 1.02746
TNF tumor necrosis factor 1.02114