Optic Neuritis Gene Set

Dataset	CTD Gene-Disease Associations
Category	disease or phenotype associations
Type	disease
Description	An optic nerve disease that results_in inflammation located_in optic nerve which may cause a complete or partial loss of vision. (Human Disease Ontology, DOID_1210)
External Link	http://ctdbase.org/detail.go?type=disease&acc=MESH:D009902
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Genes

16 genes/proteins associated with the disease Optic Neuritis from the curated CTD Gene-Disease Associations dataset.

Symbol	Name	Standardized Value
CASP3	caspase 3, apoptosis-related cysteine peptidase	1.23899
CAT	catalase	1.23042
TNF	tumor necrosis factor	1.19966
CYP3A4	cytochrome P450, family 3, subfamily A, polypeptide 4	1.16799
ABCB1	ATP-binding cassette, sub-family B (MDR/TAP), member 1	1.15223
IL6	interleukin 6	1.12872
RHPN2	rhophilin, Rho GTPase binding protein 2	1.11639
SOD2	superoxide dismutase 2, mitochondrial	1.08126
PARP1	poly (ADP-ribose) polymerase 1	1.07696
TAGLN	transgelin	1.06588
CTSL	cathepsin L	1.06297
PRL	prolactin	1.052
CEBPD	CCAAT/enhancer binding protein (C/EBP), delta	1.04427
CCL2	chemokine (C-C motif) ligand 2	1.03046
ABCC1	ATP-binding cassette, sub-family C (CFTR/MRP), member 1	1.0241
KRT8	keratin 8, type II	1.01663