CORD17 Gene

Name cone rod dystrophy 17 (autosomal dominant)
NCBI Gene ID 101409267
API
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Predicted Functions View CORD17's ARCHS4 Predicted Functions.
Co-expressed Genes View CORD17's ARCHS4 Predicted Functions.
Expression in Tissues and Cell Lines View CORD17's ARCHS4 Predicted Functions.

Functional Associations

CORD17 has 1 functional associations with biological entities spanning 1 categories (disease, phenotype or trait) extracted from 1 datasets.

Click the + buttons to view associations for CORD17 from the datasets below.

If available, associations are ranked by standardized value

Dataset Summary
OMIM Gene-Disease Associations phenotypes associated with CORD17 gene from the curated OMIM Gene-Disease Associations dataset.