|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|
|Expression in Tissues and Cell Lines||
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
|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.|