|Name||spastic paraplegia 32 (autosomal recessive)|
|NCBI Gene ID||724107|
|Expression in Tissues and Cell Lines||
SPG32 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 SPG32 from the datasets below.
If available, associations are ranked by standardized value
|CTD Gene-Disease Associations||diseases associated with SPG32 gene/protein from the curated CTD Gene-Disease Associations dataset.|
|OMIM Gene-Disease Associations||phenotypes associated with SPG32 gene from the curated OMIM Gene-Disease Associations dataset.|