hypometric saccades Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Saccadic undershoot, i.e., a saccadic eye movement that has less than the magnitude that would be required to gain fixation of the object. (Human Phenotype Ontology, HP_0000571)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0000571
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Genes

7 genes associated with the hypometric saccades phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
APTX aprataxin
DNAJC6 DnaJ (Hsp40) homolog, subfamily C, member 6
GBA glucosidase, beta, acid
GRM1 glutamate receptor, metabotropic 1
MRE11A MRE11 meiotic recombination 11 homolog A (S. cerevisiae)
NPHP1 nephronophthisis 1 (juvenile)
SPTBN2 spectrin, beta, non-erythrocytic 2