pendular nystagmus Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Rhythmic, involuntary sinusoidal oscillations of one or both eyes. The waveform of pendular nystagmus may occur in any direction. (Human Phenotype Ontology, HP_0012043)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0012043
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Genes

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

Symbol Name
AIPL1 aryl hydrocarbon receptor interacting protein-like 1
ATOH7 atonal homolog 7 (Drosophila)
CNGB3 cyclic nucleotide gated channel beta 3
CRB1 crumbs family member 1, photoreceptor morphogenesis associated
CRX cone-rod homeobox
FRMD7 FERM domain containing 7
HMGB3 high mobility group box 3
LRP5 low density lipoprotein receptor-related protein 5
NUP62 nucleoporin 62kDa
RPGRIP1 retinitis pigmentosa GTPase regulator interacting protein 1