Name | cone rod dystrophy 1 (autosomal dominant) |
Synonyms | CORD, CRD1 |
NCBI Gene ID | 1319 |
API | |
Download Associations | |
Predicted Functions |
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Co-expressed Genes |
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Expression in Tissues and Cell Lines |
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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
Dataset | Summary | |
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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. | |