Hepatitis C Gene Set

Dataset CTD Gene-Disease Associations
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)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D006526
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17 genes/proteins associated with the disease Hepatitis C from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
HFE hemochromatosis 2.88009
CCR5 chemokine (C-C motif) receptor 5 (gene/pseudogene) 2.88009
IFNL3 interferon, lambda 3 2.88009
CYP3A4 cytochrome P450, family 3, subfamily A, polypeptide 4 2.88009
PTPRC protein tyrosine phosphatase, receptor type, C 2.88009
LOX lysyl oxidase 2.88009
IFNA2 interferon, alpha 2 2.88009
SCARB1 scavenger receptor class B, member 1 2.88009
LOXL2 lysyl oxidase-like 2 2.88009
LPL lipoprotein lipase 2.88009
DDX58 DEAD (Asp-Glu-Ala-Asp) box polypeptide 58 2.88009
IFNG interferon, gamma 2.88009
CD81 CD81 molecule 2.88009
CYP2A6 cytochrome P450, family 2, subfamily A, polypeptide 6 2.88009
OPRM1 opioid receptor, mu 1 2.88009
IL4 interleukin 4 1.14541
IL2 interleukin 2 1.05386