Hepatitis B 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 B virus, which is transmitted_by sexual contact, transmitted_by blood transfusions, and transmitted_by fomites like needles or syringes. 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_2043)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D006509
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12 genes/proteins associated with the disease Hepatitis B from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
IFNB1 interferon, beta 1, fibroblast 2.88009
SLC10A1 solute carrier family 10 (sodium/bile acid cotransporter), member 1 2.88009
LOX lysyl oxidase 2.88009
IFNA1 interferon, alpha 1 2.88009
IFNA2 interferon, alpha 2 2.88009
IFNAR2 interferon (alpha, beta and omega) receptor 2 2.88009
LOXL2 lysyl oxidase-like 2 2.88009
IFNG interferon, gamma 2.88009
IL10RB interleukin 10 receptor, beta 2.88009
HP haptoglobin 2.88009
CYP2A6 cytochrome P450, family 2, subfamily A, polypeptide 6 2.88009
IFNGR1 interferon gamma receptor 1 2.88009