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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 |
|---|---|---|---|
| 5293 | PIK3CD | phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta | |
| 5294 | PIK3CG | phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma | |
| 5373 | PMM2 | phosphomannomutase 2 | |
| 5621 | PRNP | prion protein (Kanno blood group) | |
| 6785 | ELOVL4 | ELOVL fatty acid elongase 4 | |
| 8398 | PLA2G6 | phospholipase A2 group VI | |
| 9254 | CACNA2D2 | calcium voltage-gated channel auxiliary subunit alpha2delta 2 | |
| 9374 | PPT2 | palmitoyl-protein thioesterase 2 | |
| 9420 | CYP7B1 | cytochrome P450 family 7 subfamily B member 1 | |
| 10908 | PNPLA6 | patatin like phospholipase domain containing 6 |
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| Q96EG1 | Arylsulfatase G | |
| Q9GZR5 | Very long chain fatty acid elongase 4 | |
| Q9NY47 | Voltage-dependent calcium channel subunit alpha-2/delta-2 | |
| Q9NYP7 | Very long chain fatty acid elongase 5 | |
| Q9UMR5 | Lysosomal thioesterase PPT2 |
