Entity Details
Details
PrimaryID | 340990 |
RefseqGene | NG_033191 |
Symbol | OTOG |
Name | otogelin |
Chromosome | 11 |
Location | 11p15.1 |
TaxID | 9606 |
Status | live |
SourceGenome | genomic |
SourceOrigin | natural |
CreationDate | 2003-03-28 |
ModificationDate | 2021-06-11 |
Diseases
Show/Hide Table
Disease ID | Source | Name | Description |
614945 | OMIM | Deafness, autosomal recessive, 18B (DFNB18B) | A form of non-syndromic deafness characterized by a moderate hearing impairment, which can be associated with vestibular dysfunction, and a flat to shallow 'U' or slightly downsloping shaped audiograms. The disease is caused by variants affecting the gene represented in this entry. |
Interactions
2 interactions