gaze-evoked nystagmus Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Nystagmus made apparent by looking to the right or to the left. (Human Phenotype Ontology, HP_0000640)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0000640
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Genes

19 genes associated with the gaze-evoked nystagmus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
AFG3L2 AFG3-like AAA ATPase 2
APTX aprataxin
ATXN1 ataxin 1
ATXN2 ataxin 2
ATXN3 ataxin 3
BEAN1 brain expressed, associated with NEDD4, 1
CACNA1A calcium channel, voltage-dependent, P/Q type, alpha 1A subunit
CACNB4 calcium channel, voltage-dependent, beta 4 subunit
FGF14 fibroblast growth factor 14
ITPR1 inositol 1,4,5-trisphosphate receptor, type 1
KCND3 potassium channel, voltage gated Shal related subfamily D, member 3
MRE11A MRE11 meiotic recombination 11 homolog A (S. cerevisiae)
SCN8A sodium channel, voltage gated, type VIII alpha subunit
SETX senataxin
SPG11 spastic paraplegia 11 (autosomal recessive)
SPTBN2 spectrin, beta, non-erythrocytic 2
TBP TATA box binding protein
VLDLR very low density lipoprotein receptor
WWOX WW domain containing oxidoreductase