SPG29 Gene

Name spastic paraplegia 29 (autosomal dominant)
NCBI Gene ID 619379
API
Download Associations
Predicted Functions View SPG29's ARCHS4 Predicted Functions.
Co-expressed Genes View SPG29's ARCHS4 Predicted Functions.
Expression in Tissues and Cell Lines View SPG29's ARCHS4 Predicted Functions.

Functional Associations

SPG29 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 SPG29 from the datasets below.

If available, associations are ranked by standardized value

Dataset Summary
CTD Gene-Disease Associations diseases associated with SPG29 gene/protein from the curated CTD Gene-Disease Associations dataset.
OMIM Gene-Disease Associations phenotypes associated with SPG29 gene from the curated OMIM Gene-Disease Associations dataset.