abnormality of saccadic eye movements Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormality of eye movement characterized by impairment of fast (saccadic) eye movements. (Human Phenotype Ontology, HP_0000570)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0000570
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31 genes associated with the abnormality of saccadic eye movements phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
AFG3L2 AFG3-like AAA ATPase 2
ANO10 anoctamin 10
APTX aprataxin
ATP13A2 ATPase type 13A2
ATXN1 ataxin 1
ATXN2 ataxin 2
ATXN3 ataxin 3
ATXN7 ataxin 7
ATXN8 ataxin 8
ATXN8OS ATXN8 opposite strand (non-protein coding)
DNAJC6 DnaJ (Hsp40) homolog, subfamily C, member 6
EEF2 eukaryotic translation elongation factor 2
ELOVL5 ELOVL fatty acid elongase 5
FBXO7 F-box protein 7
FGF14 fibroblast growth factor 14
GBA glucosidase, beta, acid
GJC2 gap junction protein, gamma 2, 47kDa
GRM1 glutamate receptor, metabotropic 1
INPP5E inositol polyphosphate-5-phosphatase, 72 kDa
ITPR1 inositol 1,4,5-trisphosphate receptor, type 1
MFN2 mitofusin 2
MRE11A MRE11 meiotic recombination 11 homolog A (S. cerevisiae)
NOP56 NOP56 ribonucleoprotein
NPHP1 nephronophthisis 1 (juvenile)
PDYN prodynorphin
PIK3R5 phosphoinositide-3-kinase, regulatory subunit 5
SCP2 sterol carrier protein 2
SPTBN2 spectrin, beta, non-erythrocytic 2
TMEM216 transmembrane protein 216
TPP1 tripeptidyl peptidase I
VAMP1 vesicle-associated membrane protein 1 (synaptobrevin 1)