DFNA49 Gene

Name deafness, autosomal dominant 49
NCBI Gene ID 317664
API
Download Associations
Predicted Functions View DFNA49's ARCHS4 Predicted Functions.
Co-expressed Genes View DFNA49's ARCHS4 Predicted Functions.
Expression in Tissues and Cell Lines View DFNA49's ARCHS4 Predicted Functions.

Functional Associations

DFNA49 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 DFNA49 from the datasets below.

If available, associations are ranked by standardized value

Dataset Summary
CTD Gene-Disease Associations diseases associated with DFNA49 gene/protein from the curated CTD Gene-Disease Associations dataset.
OMIM Gene-Disease Associations phenotypes associated with DFNA49 gene from the curated OMIM Gene-Disease Associations dataset.