DFNA58 Gene

Name deafness, autosomal dominant 58
Description This locus was identified to map between markers D2S2259 and D2S2114 in a Brazilian family with 12 individuals affected by bilateral post-lingual and progressive hearing loss. [provided by RefSeq, Feb 2010]
NCBI Gene ID 100359395
API
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Predicted Functions View DFNA58's ARCHS4 Predicted Functions.
Co-expressed Genes View DFNA58's ARCHS4 Predicted Functions.
Expression in Tissues and Cell Lines View DFNA58's ARCHS4 Predicted Functions.

Functional Associations

DFNA58 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 DFNA58 from the datasets below.

If available, associations are ranked by standardized value

Dataset Summary
OMIM Gene-Disease Associations phenotypes associated with DFNA58 gene from the curated OMIM Gene-Disease Associations dataset.