Abnormal Involuntary Eye Movements Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Anomalous movements of the eyes that occur without the subject wanting them to happen. (Human Phenotype Ontology, HP_0012547)
External Link https://www.disgenet.org/browser/0/1/0/C4022855
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Genes

6 genes associated with the disease Abnormal Involuntary Eye Movements in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
BRAF B-Raf proto-oncogene, serine/threonine kinase
GM2A GM2 ganglioside activator
GRIN2A glutamate receptor, ionotropic, N-methyl D-aspartate 2A
HTT huntingtin
MECP2 methyl CpG binding protein 2
PAX6 paired box 6