RP32 Gene

Name retinitis pigmentosa 32 (autosomal recessive)
NCBI Gene ID 641433
API
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Predicted Functions View RP32's ARCHS4 Predicted Functions.
Co-expressed Genes View RP32's ARCHS4 Predicted Functions.
Expression in Tissues and Cell Lines View RP32's ARCHS4 Predicted Functions.

Functional Associations

RP32 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 RP32 from the datasets below.

If available, associations are ranked by standardized value

Dataset Summary
CTD Gene-Disease Associations diseases associated with RP32 gene/protein from the curated CTD Gene-Disease Associations dataset.
OMIM Gene-Disease Associations phenotypes associated with RP32 gene from the curated OMIM Gene-Disease Associations dataset.