DFNB83 Gene

Name deafness, autosomal recessive 83
Description This locus, identified by homozygosity mapping, overlaps that of DFNA47. It may be that mutations of the same gene are responsible for recessive and dominant hearing loss. [provided by RefSeq, Feb 2010]
NCBI Gene ID 100359400
API
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Predicted Functions View DFNB83's ARCHS4 Predicted Functions.
Co-expressed Genes View DFNB83's ARCHS4 Predicted Functions.
Expression in Tissues and Cell Lines View DFNB83's ARCHS4 Predicted Functions.

Functional Associations

DFNB83 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 DFNB83 from the datasets below.

If available, associations are ranked by standardized value

Dataset Summary
CTD Gene-Disease Associations diseases associated with DFNB83 gene/protein from the curated CTD Gene-Disease Associations dataset.
OMIM Gene-Disease Associations phenotypes associated with DFNB83 gene from the curated OMIM Gene-Disease Associations dataset.