SPG41 Gene

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
API
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Predicted Functions View SPG41's ARCHS4 Predicted Functions.
Co-expressed Genes View SPG41's ARCHS4 Predicted Functions.
Expression in Tissues and Cell Lines View SPG41's ARCHS4 Predicted Functions.

Functional Associations

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.