impaired horizontal smooth pursuit Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormality of ocular smooth pursuit characterized by an impairment of the ability to track horizontally moving objects. (Human Phenotype Ontology, HP_0001151)
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6 genes associated with the impaired horizontal smooth pursuit phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ATXN1 ataxin 1
ATXN2 ataxin 2
ATXN3 ataxin 3
EEF2 eukaryotic translation elongation factor 2
POLR3B polymerase (RNA) III (DNA directed) polypeptide B
STXBP1 syntaxin binding protein 1