SPG38 Gene

Name spastic paraplegia 38 (autosomal dominant, Silver syndrome)
NCBI Gene ID 100049707
API
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Predicted Functions View SPG38's ARCHS4 Predicted Functions.
Co-expressed Genes View SPG38's ARCHS4 Predicted Functions.
Expression in Tissues and Cell Lines View SPG38's ARCHS4 Predicted Functions.

Functional Associations

SPG38 has 17 functional associations with biological entities spanning 2 categories (disease, phenotype or trait, functional term, phrase or reference) extracted from 3 datasets.

Click the + buttons to view associations for SPG38 from the datasets below.

If available, associations are ranked by standardized value

Dataset Summary
CTD Gene-Disease Associations diseases associated with SPG38 gene/protein from the curated CTD Gene-Disease Associations dataset.
GeneRIF Biological Term Annotations biological terms co-occuring with SPG38 gene in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
OMIM Gene-Disease Associations phenotypes associated with SPG38 gene from the curated OMIM Gene-Disease Associations dataset.