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| References | OMIM | Gene | GeneReviews | HGMD | HGNC |
| GENATLAS PHENOTYPE |
| last update : 15/06/2006 |
| Symbol | BOS3 |
| Location | 14q21.3-q24.3 |
| Name | branchio-otic syndrome 3 |
| Other name(s) | BO syndrome 3 |
| Corresponding gene | SIX1 |
| Main clinical features |
|
| Genetic determination | autosomal dominant |
| Function/system disorder | ear |
| dermatology | |
| Type | disease |
| Gene product |
| Name | sine oculis homeobox homolog 1 |
| Remark(s) |