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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
cerebellar ataxia
Summary
- Definition
- A hereditary ataxia that is characterized by ataxia originating in the cerebellum.
- Super Class
- cerebellar disease hereditary ataxia
External Links
- Disease Ontology
- DOID:0050753
- Mondo Disease Ontology
- MeSH
- MGI genotype (from TogoID)
Related Genes
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 16 | AARS1 | alanyl-tRNA synthetase 1 | |
| 773 | CACNA1A | calcium voltage-gated channel subunit alpha1 A | |
| 10908 | PNPLA6 | patatin like phospholipase domain containing 6 | |
| 23230 | VPS13A | vacuolar protein sorting 13 homolog A | |
| 23322 | RPGRIP1L | RPGRIP1 like | |
| 23345 | SYNE1 | spectrin repeat containing nuclear envelope protein 1 | |
| 25929 | GEMIN5 | gem nuclear organelle associated protein 5 | |
| 54832 | VPS13C | vacuolar protein sorting 13 homolog C | |
| 57505 | AARS2 | alanyl-tRNA synthetase 2, mitochondrial | |
| 79944 | L2HGDH | L-2-hydroxyglutarate dehydrogenase |
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 12286 | Cacna1a | calcium channel, voltage-dependent, P/Q type, alpha 1A subunit | |
| 50767 | Pnpla6 | patatin-like phospholipase domain containing 6 | |
| 64009 | Syne1 | spectrin repeat containing, nuclear envelope 1 | |
| 216766 | Gemin5 | gem nuclear organelle associated protein 5 | |
| 234734 | Aars1 | alanyl-tRNA synthetase 1 | |
| 271564 | Vps13a | vacuolar protein sorting 13A | |
| 320528 | Vps13c | vacuolar protein sorting 13C |
