| Name | spinocerebellar ataxia 18 (sensory with neurogenic muscular atrophy) |
| Synonyms | SMNA |
| NCBI Gene ID | 94008 |
| API | |
| Download Associations | |
| Predicted Functions |
 |
| Co-expressed Genes |
|
| Expression in Tissues and Cell Lines |
|
SCA18 has 5 functional associations with biological entities spanning 1 categories (disease, phenotype or trait) extracted from 5 datasets.
Click the + buttons to view associations for SCA18 from the datasets below.
If available, associations are ranked by standardized value
| Dataset | Summary | |
|---|---|---|
| CTD Gene-Disease Associations | diseases associated with SCA18 gene/protein from the curated CTD Gene-Disease Associations dataset. | |
| GAD Gene-Disease Associations | diseases associated with SCA18 gene in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. | |
| GAD High Level Gene-Disease Associations | diseases associated with SCA18 gene in GWAS and other genetic association datasets from the GAD High Level Gene-Disease Associations dataset. | |
| HuGE Navigator Gene-Phenotype Associations | phenotypes associated with SCA18 gene by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. | |
| OMIM Gene-Disease Associations | phenotypes associated with SCA18 gene from the curated OMIM Gene-Disease Associations dataset. | |
