Rubella Gene Set

Dataset HuGE Navigator Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description A viral infectious disease that results_in infection located_in skin, has_material_basis_in Rubella virus, which is transmitted_by droplet spread of oronasal secretions from the infected person through coughing and sneezing, and transmitted_by congenital method. The infection has_symptom rash on the face which spreads to the trunk and limbs, has_symptom fever, has_symptom lymphadenopathy, has_symptom joint pains, has_symptom headache, and has_symptom conjunctivitis. (Human Disease Ontology, DOID_8781)
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19 genes associated with the Rubella phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Symbol Name
ADAR adenosine deaminase, RNA-specific
BTN2A1 butyrophilin, subfamily 2, member A1
BTN3A3 butyrophilin, subfamily 3, member A3
IFNAR2 interferon (alpha, beta and omega) receptor 2
IFNB1 interferon, beta 1, fibroblast
IL10RB interleukin 10 receptor, beta
IL12B interleukin 12B
IL12RB2 interleukin 12 receptor, beta 2
IL18R1 interleukin 18 receptor 1
IL1B interleukin 1, beta
IL1RN interleukin 1 receptor antagonist
IL2RA interleukin 2 receptor, alpha
IL2RB interleukin 2 receptor, beta
IL4R interleukin 4 receptor
IL6 interleukin 6
PVR poliovirus receptor
TNF tumor necrosis factor
TNFRSF1A tumor necrosis factor receptor superfamily, member 1A
TNFRSF1B tumor necrosis factor receptor superfamily, member 1B