DFNB83 (-)
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Gene
Gene information from NCBI Gene database.
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| Entrez ID | 100359400 |
| Gene name | - |
| Gene symbol | DFNB83 |
| Synonyms (NCBI Gene) |
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| Chromosome | 9 |
| Chromosome location | 9p23-p21.2 |
| Summary | 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] |
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Other IDs
Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
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Related Genes
Genes most often co-reported with DFNB83 across shared curated disease and pathway associations.
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Diseases Linked via Similar Genes
Diseases curated for genes most similar to DFNB83 (see Related Genes above), that are NOT already directly curated for DFNB83 itself -- a lead worth checking, not a confirmed association.
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