OASD Gene

Name ocular albinism and sensorineural deafness
NCBI Gene ID 4941
API
Download Associations
Predicted Functions View OASD's ARCHS4 Predicted Functions.
Co-expressed Genes View OASD's ARCHS4 Predicted Functions.
Expression in Tissues and Cell Lines View OASD's ARCHS4 Predicted Functions.

Functional Associations

OASD 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 OASD from the datasets below.

If available, associations are ranked by standardized value

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