slow saccadic eye movements Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormally slow velocity of the saccadic eye movements. (Human Phenotype Ontology, HP_0000514)
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15 genes associated with the slow 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
ATP13A2 ATPase type 13A2
ATXN1 ataxin 1
ATXN2 ataxin 2
ATXN7 ataxin 7
ATXN8 ataxin 8
ATXN8OS ATXN8 opposite strand (non-protein coding)
ELOVL5 ELOVL fatty acid elongase 5
FBXO7 F-box protein 7
GBA glucosidase, beta, acid
GJC2 gap junction protein, gamma 2, 47kDa
NOP56 NOP56 ribonucleoprotein
PDYN prodynorphin
PIK3R5 phosphoinositide-3-kinase, regulatory subunit 5
VAMP1 vesicle-associated membrane protein 1 (synaptobrevin 1)