hepatitis c Gene Set

Dataset DISEASES Experimental Gene-Disease Association Evidence Scores
Category disease or phenotype associations
Type disease
Description A viral infectious disease that results_in inflammation located_in liver, has_material_basis_in Hepatitis C virus, which is transmitted_by blood from an infected person enters the body of an uninfected person. The infection has_symptom fever, has_symptom fatigue, has_symptom loss of appetite, has_symptom nausea, has_symptom vomiting, has_symptom abdominal pain, has_symptom clay-colored bowel movements, has_symptom joint pain, and has_symptom jaundice. (Human Disease Ontology, DOID_1883)
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Genes

15 genes associated with the disease hepatitis c in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
IFNL3 interferon, lambda 3 1.70133
ITPA inosine triphosphatase (nucleoside triphosphate pyrophosphatase) 1.58223
DDRGK1 DDRGK domain containing 1 1.55692
HLA-DQA2 major histocompatibility complex, class II, DQ alpha 2 1.20753
DEPDC5 DEP domain containing 5 0.965481
NPS neuropeptide S 0.327313
OLFM1 olfactomedin 1 0.256228
EFCAB14 EF-hand calcium binding domain 14 0.256228
SLC22A3 solute carrier family 22 (organic cation transporter), member 3 0.197766
ARHGEF10L Rho guanine nucleotide exchange factor (GEF) 10-like 0.15771
SCG2 secretogranin II 0.15771
AK9 adenylate kinase 9 0.064973
DNASE2B deoxyribonuclease II beta 0.064973
EPHA7 EPH receptor A7 0.064973
CWH43 cell wall biogenesis 43 C-terminal homolog (S. cerevisiae) 0.052255