| Name | spastic paraplegia 41 (autosomal dominant) |
| Description | This locus was defined in a Chinese family. Nineteen individuals were genotyped and the interval was defined between D11S1324 and D11S1933. [provided by RefSeq, Feb 2010] |
| NCBI Gene ID | 100359402 |
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| Predicted Functions |
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| Co-expressed Genes |
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| Expression in Tissues and Cell Lines |
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SPG41 has 4 functional associations with biological entities spanning 1 categories (disease, phenotype or trait) extracted from 4 datasets.
Click the + buttons to view associations for SPG41 from the datasets below.
If available, associations are ranked by standardized value
| Dataset | Summary | |
|---|---|---|
| CTD Gene-Disease Associations | diseases associated with SPG41 gene/protein from the curated CTD Gene-Disease Associations dataset. | |
| GAD Gene-Disease Associations | diseases associated with SPG41 gene in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. | |
| HuGE Navigator Gene-Phenotype Associations | phenotypes associated with SPG41 gene by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. | |
| OMIM Gene-Disease Associations | phenotypes associated with SPG41 gene from the curated OMIM Gene-Disease Associations dataset. | |
