| Dataset | HPO Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | The controller signal for saccadic eye movements has two components: the pulse that moves the eye rapidly from one point to the next, and the step that holds the eye in the new position. When both the pulse and the step are not the correct size, a dysmetric refixation eye movement results. (Human Phenotype Ontology, HP_0000641) |
| External Link | http://compbio.charite.de/hpoweb/showterm?id=HP:0000641 |
| Similar Terms | |
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10 genes associated with the dysmetric saccades phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| AFG3L2 | AFG3-like AAA ATPase 2 |
| ATXN1 | ataxin 1 |
| ATXN2 | ataxin 2 |
| ATXN3 | ataxin 3 |
| ATXN8 | ataxin 8 |
| ATXN8OS | ATXN8 opposite strand (non-protein coding) |
| EEF2 | eukaryotic translation elongation factor 2 |
| FGF14 | fibroblast growth factor 14 |
| ITPR1 | inositol 1,4,5-trisphosphate receptor, type 1 |
| MFN2 | mitofusin 2 |
