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This section gives an overview of the disease, and where available shows the following:
More information can be found in the help pages.
✖Disease ID: | 879 | |
Name: | Spinocerebellar ataxia 19; SCA19 | |
Associated with: | 1 target |
Synonyms |
Spinocerebellar ataxia 22; SCA22 | Spinocerebellar ataxia type 19/22 |
Database Links |
OMIM:
607346 Orphanet: ORPHA98772 |
Click on the target name to link to its detailed view page
Where available, information is display on the role of the target in the disease; drugs which target the disease and their therapeutic use and side-effects.
If there is mutation data curated in GtoPdb this is indicated, with a link back to the appropriate section on the target detailed view page
Immuno ligand interactions - If available, a table of immuno-relevant ligands is shown. These ligands have been curated as having an association to the disease and possess interaction data with the target in GtoPdb. The approval status of the ligand is shown, along with curator comments and an indication of whether the target is considered the primary target of the ligand.
More information can be found in the help pages.
✖Kv4.3 | |
References: | 1-3 |
Mutations: | Kv4.3 is associated with 3 mutation. Click here for details ![]() |
Click ligand name to view ligand summary page
Click the arrow in the final column to expand comments
More information can be found in the help pages.
✖No ligand related data available for Spinocerebellar ataxia 19; SCA19
1. Duarri A, Jezierska J, Fokkens M, Meijer M, Schelhaas HJ, den Dunnen WF, van Dijk F, Verschuuren-Bemelmans C, Hageman G, van de Vlies P et al.. (2012) Mutations in potassium channel kcnd3 cause spinocerebellar ataxia type 19. Ann Neurol, 72 (6): 870-80. [PMID:23280838]
2. Lee YC, Durr A, Majczenko K, Huang YH, Liu YC, Lien CC, Tsai PC, Ichikawa Y, Goto J, Monin ML et al.. (2012) Mutations in KCND3 cause spinocerebellar ataxia type 22. Ann Neurol, 72 (6): 859-69. [PMID:23280837]
3. Pulst SM, Otis TS. (2012) Repolarization matters: mutations in the Kv4.3 potassium channel cause SCA19/22. Ann Neurol, 72 (6): 829-31. [PMID:23280833]