abnormality of ocular smooth pursuit Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormality of eye movement characterized by impaired smooth-pursuit eye movements. (Human Phenotype Ontology, HP_0000617)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0000617
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29 genes associated with the abnormality of ocular 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)
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
FMR1 fragile X mental retardation 1
GBA2 glucosidase, beta (bile acid) 2
INPP5E inositol polyphosphate-5-phosphatase, 72 kDa
ITPR1 inositol 1,4,5-trisphosphate receptor, type 1
KCND3 potassium channel, voltage gated Shal related subfamily D, member 3
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
SETX senataxin
SPTBN2 spectrin, beta, non-erythrocytic 2
STXBP1 syntaxin binding protein 1
SYT14 synaptotagmin XIV
TBP TATA box binding protein
TMEM216 transmembrane protein 216
TPP1 tripeptidyl peptidase I
TSEN54 TSEN54 tRNA splicing endonuclease subunit