neuromyelitis optica Gene Set

Dataset GWASdb SNP-Disease Associations
Category disease or phenotype associations
Type disease
Description A central nervous system disease characterized by acute neuritis located_in eye and demyelination located_in optic nerve and located_in spinal cord. (Human Disease Ontology, DOID_8869)
External Link http://jjwanglab.org/gwasdb/gwasdb2/gwasdb2/go_trait/DOID:8869
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Genes

15 genes associated with the disease neuromyelitis optica in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

Symbol Name Standardized Value
ADARB2 adenosine deaminase, RNA-specific, B2 (non-functional) 0.996743
IL22RA2 interleukin 22 receptor, alpha 2 0.986376
CNTNAP2 contactin associated protein-like 2 0.937304
BRPF3 bromodomain and PHD finger containing, 3 0.912987
CYP7A1 cytochrome P450, family 7, subfamily A, polypeptide 1 0.912987
KCNH1 potassium channel, voltage gated eag related subfamily H, member 1 0.905653
DPYD dihydropyrimidine dehydrogenase 0.874542
ATP7B ATPase, Cu++ transporting, beta polypeptide 0.831584
ADRA1A adrenoceptor alpha 1A 0.819144
TNFRSF11A tumor necrosis factor receptor superfamily, member 11a, NFKB activator 0.808055
UTP14C UTP14, U3 small nucleolar ribonucleoprotein, homolog C (yeast) 0.804621
NCK2 NCK adaptor protein 2 0.790866
ALG11 ALG11, alpha-1,2-mannosyltransferase 0.787593
SPACA7 sperm acrosome associated 7 0.78442
FHL3 four and a half LIM domains 3 0.772631