|Name||cone rod dystrophy 1 (autosomal dominant)|
|NCBI Gene ID||1319|
|Expression in Tissues and Cell Lines||
CORD1 has 9 functional associations with biological entities spanning 2 categories (disease, phenotype or trait, gene, protein or microRNA) extracted from 3 datasets.
Click the + buttons to view associations for CORD1 from the datasets below.
If available, associations are ranked by standardized value
|CTD Gene-Disease Associations||diseases associated with CORD1 gene/protein from the curated CTD Gene-Disease Associations dataset.|
|Hub Proteins Protein-Protein Interactions||interacting hub proteins for CORD1 from the curated Hub Proteins Protein-Protein Interactions dataset.|
|OMIM Gene-Disease Associations||phenotypes associated with CORD1 gene from the curated OMIM Gene-Disease Associations dataset.|