impaired smooth pursuit Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An impairment of the ability to track objects with the ocular smooth pursuit system, a class of rather slow eye movements that minimizes retinal target motion. (Human Phenotype Ontology, HP_0007772)
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22 genes associated with the impaired 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
ATXN8 ataxin 8
ATXN8OS ATXN8 opposite strand (non-protein coding)
CACNA1A calcium channel, voltage-dependent, P/Q type, alpha 1A subunit
EEF2 eukaryotic translation elongation factor 2
FGF14 fibroblast growth factor 14
INPP5E inositol polyphosphate-5-phosphatase, 72 kDa
ITPR1 inositol 1,4,5-trisphosphate receptor, type 1
MAN2B1 mannosidase, alpha, class 2B, member 1
MRE11A MRE11 meiotic recombination 11 homolog A (S. cerevisiae)
NOP56 NOP56 ribonucleoprotein
PLA2G6 phospholipase A2, group VI (cytosolic, calcium-independent)
POLR3B polymerase (RNA) III (DNA directed) polypeptide B
PRNP prion protein
SACS sacsin molecular chaperone
SPTBN2 spectrin, beta, non-erythrocytic 2
STXBP1 syntaxin binding protein 1
SYT14 synaptotagmin XIV
TMEM216 transmembrane protein 216
TSEN54 TSEN54 tRNA splicing endonuclease subunit