Borna Disease Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A viral infectious disease that results_in infection, which affects dopaminergic neurotransmission located_in central nervous system, has_material_basis_in Borna disease virus, which is transmitted_by contact with infected oronasal secretions. The infection has_symptom mood disturbances, has_symptom behaviour disturbances, has_symptom cognitive disturbances, has_symptom neurologic disturbances, and has_symptom movement impairment. (Human Disease Ontology, DOID_5154)
External Link https://www.disgenet.org/browser/0/1/0/C0006023
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Genes

23 genes associated with the disease Borna Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ACTB actin, beta
ALDOC aldolase C, fructose-bisphosphate
CD44 CD44 molecule (Indian blood group)
CD9 CD9 molecule
CHP1 calcineurin-like EF-hand protein 1
CX3CL1 chemokine (C-X3-C motif) ligand 1
CX3CR1 chemokine (C-X3-C motif) receptor 1
GJA1 gap junction protein, alpha 1, 43kDa
GJB6 gap junction protein, beta 6, 30kDa
IL16 interleukin 16
IRF7 interferon regulatory factor 7
KMO kynurenine 3-monooxygenase (kynurenine 3-hydroxylase)
MIF macrophage migration inhibitory factor (glycosylation-inhibiting factor)
MT3 metallothionein 3
NRSN1 neurensin 1
OCA2 oculocutaneous albinism II
PARG poly (ADP-ribose) glycohydrolase
PARP1 poly (ADP-ribose) polymerase 1
PENK proenkephalin
RAB5A RAB5A, member RAS oncogene family
S100B S100 calcium binding protein B
TMED2 transmembrane emp24 domain trafficking protein 2
TPPP tubulin polymerization promoting protein