| Dataset | MPO Gene-Phenotype Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | Aplasia of the stapes. (Human Phenotype Ontology, HP_0011456) |
| External Link | http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004204 |
| Similar Terms | |
| Downloads & Tools |
11 gene mutations causing the absent stapes phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
| Symbol | Name |
|---|---|
| DLX5 | distal-less homeobox 5 |
| ECE1 | endothelin converting enzyme 1 |
| EDNRA | endothelin receptor type A |
| EYA1 | EYA transcriptional coactivator and phosphatase 1 |
| FOXC2 | forkhead box C2 |
| FOXI3 | forkhead box I3 |
| HOXA1 | homeobox A1 |
| HOXA2 | homeobox A2 |
| PBX1 | pre-B-cell leukemia homeobox 1 |
| SIX1 | SIX homeobox 1 |
| TBX1 | T-box 1 |
