SPG19 Gene

Name spastic paraplegia 19 (autosomal dominant)
NCBI Gene ID 140907
API
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Predicted Functions View SPG19's ARCHS4 Predicted Functions.
Co-expressed Genes View SPG19's ARCHS4 Predicted Functions.
Expression in Tissues and Cell Lines View SPG19's ARCHS4 Predicted Functions.

Functional Associations

SPG19 has 11 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 SPG19 from the datasets below.

If available, associations are ranked by standardized value

Dataset Summary
CTD Gene-Disease Associations diseases associated with SPG19 gene/protein from the curated CTD Gene-Disease Associations dataset.
GeneRIF Biological Term Annotations biological terms co-occuring with SPG19 gene in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
OMIM Gene-Disease Associations phenotypes associated with SPG19 gene from the curated OMIM Gene-Disease Associations dataset.