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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
autosomal dominant cerebellar ataxia
Summary
- Synonym
-
- spinocerebellar ataxia
- Definition
- A cerebellar ataxia that has_material_basis_in autosomal dominant inheritance.
- Super Class
- autosomal dominant disease cerebellar ataxia
Related Genes
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 8630 | HSD17B6 | hydroxysteroid 17-beta dehydrogenase 6 | |
| 10724 | OGA | O-GlcNAcase | |
| 10908 | PNPLA6 | patatin like phospholipase domain containing 6 | |
| 11181 | TREH | trehalase | |
| 27306 | HPGDS | hematopoietic prostaglandin D synthase | |
| 55304 | SPTLC3 | serine palmitoyltransferase long chain base subunit 3 | |
| 60481 | ELOVL5 | ELOVL fatty acid elongase 5 | |
| 151056 | PLB1 | phospholipase B1 | |
| 152330 | CNTN4 | contactin 4 | |
| 285362 | SUMF1 | sulfatase modifying factor 1 |
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| O14756 | 17-beta-hydroxysteroid dehydrogenase type 6 | |
| O43280 | Trehalase | |
| O60502 | Protein O-GlcNAcase | |
| O60760 | Hematopoietic prostaglandin D synthase | |
| P04040 | Catalase | |
| P04156 | Major prion protein | |
| P14555 | Phospholipase A2, membrane associated | |
| P34949 | Mannose-6-phosphate isomerase | |
| Q04760 | Lactoylglutathione lyase | |
| Q13822 | Ectonucleotide pyrophosphatase/phosphodiesterase family member 2 |
