saccadic smooth pursuit Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormality of tracking eye movements in which smooth pursuit is interrupted by an abnormally high number of saccadic movements. (Human Phenotype Ontology, HP_0001152)
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6 genes associated with the saccadic smooth pursuit phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ALS2 amyotrophic lateral sclerosis 2 (juvenile)
CACNA1A calcium channel, voltage-dependent, P/Q type, alpha 1A subunit
FMR1 fragile X mental retardation 1
KCND3 potassium channel, voltage gated Shal related subfamily D, member 3
SETX senataxin
TPP1 tripeptidyl peptidase I