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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: | 892 | |
Name: | Stroke, ischemic | |
Associated with: | 4 targets |
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.
✖CELSR1 | |
References: | 1,3 |
protein kinase C eta | |
Comments: | A non-synonymous SNP in PRKCH causes susceptibility to cerebral infarction. |
References: | 2 |
Mutations: | protein kinase C eta is associated with 1 mutation. Click here for details |
coagulation factor II, thrombin |
coagulation factor V |
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 Stroke, ischemic
1. Gouveia LO, Sobral J, Vicente AM, Ferro JM, Oliveira SA. (2011) Replication of the CELSR1 association with ischemic stroke in a Portuguese case-control cohort. Atherosclerosis, 217 (1): 260-2. [PMID:21511255]
2. Kubo M, Hata J, Ninomiya T, Matsuda K, Yonemoto K, Nakano T, Matsushita T, Yamazaki K, Ohnishi Y, Saito S et al.. (2007) A nonsynonymous SNP in PRKCH (protein kinase C eta) increases the risk of cerebral infarction. Nat Genet, 39 (2): 212-7. [PMID:17206144]
3. Yamada Y, Fuku N, Tanaka M, Aoyagi Y, Sawabe M, Metoki N, Yoshida H, Satoh K, Kato K, Watanabe S, Nozawa Y, Hasegawa A, Kojima T. (2009) Identification of CELSR1 as a susceptibility gene for ischemic stroke in Japanese individuals by a genome-wide association study. Atherosclerosis, 207 (1): 144-9. [PMID:19403135]