SPG27 Gene

Name spastic paraplegia 27 (autosomal recessive)
NCBI Gene ID 414886
API
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Predicted Functions View SPG27's ARCHS4 Predicted Functions.
Co-expressed Genes View SPG27's ARCHS4 Predicted Functions.
Expression in Tissues and Cell Lines View SPG27's ARCHS4 Predicted Functions.

Functional Associations

SPG27 has 2 functional associations with biological entities spanning 1 categories (disease, phenotype or trait) extracted from 2 datasets.

Click the + buttons to view associations for SPG27 from the datasets below.

If available, associations are ranked by standardized value

Dataset Summary
CTD Gene-Disease Associations diseases associated with SPG27 gene/protein from the curated CTD Gene-Disease Associations dataset.
OMIM Gene-Disease Associations phenotypes associated with SPG27 gene from the curated OMIM Gene-Disease Associations dataset.