Opsoclonus Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Spontaneous, non-rhythmic, multi-directional, chaotic movements of the eyes, giving the appearance of agitation. There may be bursts of conjugate movement of the eyes in varying directions and of varying amplitude. (Human Phenotype Ontology, HP_0010543)
External Link https://www.disgenet.org/browser/0/1/0/C0242567
Similar Terms
Downloads & Tools

Genes

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

Symbol Name
CLCN7 chloride channel, voltage-sensitive 7
KIF1B kinesin family member 1B
SNX10 sorting nexin 10
TCIRG1 T-cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 subunit A3
TNFSF11 tumor necrosis factor (ligand) superfamily, member 11