DFNB38 Gene

Name deafness, autosomal recessive 38
NCBI Gene ID 337991
Download Associations
Predicted Functions View DFNB38's ARCHS4 Predicted Functions.
Co-expressed Genes View DFNB38's ARCHS4 Predicted Functions.
Expression in Tissues and Cell Lines View DFNB38's ARCHS4 Predicted Functions.

Functional Associations

DFNB38 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 DFNB38 from the datasets below.

If available, associations are ranked by standardized value

Dataset Summary
CTD Gene-Disease Associations diseases associated with DFNB38 gene/protein from the curated CTD Gene-Disease Associations dataset.
OMIM Gene-Disease Associations phenotypes associated with DFNB38 gene from the curated OMIM Gene-Disease Associations dataset.