| Dataset | MPO Gene-Phenotype Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | missing the upper bony framework of the mouth where the superior teeth are held (Mammalian Phenotype Ontology, MP_0004539) |
| External Link | http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004539 |
| Similar Terms | |
| Downloads & Tools |
6 gene mutations causing the absent maxilla phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
| Symbol | Name |
|---|---|
| CTNNBIP1 | catenin, beta interacting protein 1 |
| DKK1 | dickkopf WNT signaling pathway inhibitor 1 |
| EYA1 | EYA transcriptional coactivator and phosphatase 1 |
| MKS1 | Meckel syndrome, type 1 |
| OTX2 | orthodenticle homeobox 2 |
| TFAP2A | transcription factor AP-2 alpha (activating enhancer binding protein 2 alpha) |
