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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
hereditary ataxia
Summary
- Definition
- A neurodegenerative disease that is characterized by slowly progressive incoordination of gait and often associated with poor coordination of hands, speech, and eye movements.
- Super Class
- neurodegenerative disease
External Links
- Disease Ontology
- DOID:0050951
- GARD
- MGI genotype (from TogoID)
- WikiPathways (from TogoID)
Related Genes
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 773 | CACNA1A | calcium voltage-gated channel subunit alpha1 A | |
| 774 | CACNA1B | calcium voltage-gated channel subunit alpha1 B | |
| 777 | CACNA1E | calcium voltage-gated channel subunit alpha1 E | |
| 10531 | PITRM1 | pitrilysin metallopeptidase 1 | |
| 57410 | SCYL1 | SCY1 like pseudokinase 1 |
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 555941 | cacna1ba | calcium channel, voltage-dependent, N type, alpha 1B subunit, a | |
| 562059 | cacna1aa | calcium channel, voltage-dependent, P/Q type, alpha 1A subunit, a | |
| 569528 | cacna1ab | calcium channel, voltage-dependent, P/Q type, alpha 1A subunit, b |
