DFNB13 Gene

Name deafness, autosomal recessive 13
NCBI Gene ID 1705
API
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Predicted Functions View DFNB13's ARCHS4 Predicted Functions.
Co-expressed Genes View DFNB13's ARCHS4 Predicted Functions.
Expression in Tissues and Cell Lines View DFNB13's ARCHS4 Predicted Functions.

Functional Associations

DFNB13 has 12 functional associations with biological entities spanning 2 categories (disease, phenotype or trait, functional term, phrase or reference) extracted from 4 datasets.

Click the + buttons to view associations for DFNB13 from the datasets below.

If available, associations are ranked by standardized value

Dataset Summary
CTD Gene-Disease Associations diseases associated with DFNB13 gene/protein from the curated CTD Gene-Disease Associations dataset.
GeneRIF Biological Term Annotations biological terms co-occuring with DFNB13 gene in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
HuGE Navigator Gene-Phenotype Associations phenotypes associated with DFNB13 gene by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
OMIM Gene-Disease Associations phenotypes associated with DFNB13 gene from the curated OMIM Gene-Disease Associations dataset.