| Dataset | MPO Gene-Phenotype Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | A developmental defect in which the legs are fused together. (Human Phenotype Ontology, HP_0010497) |
| External Link | http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003445 |
| Similar Terms | |
| Downloads & Tools |
5 gene mutations causing the sirenomelia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
| Symbol | Name |
|---|---|
| CYP26A1 | cytochrome P450, family 26, subfamily A, polypeptide 1 |
| DACT1 | dishevelled-binding antagonist of beta-catenin 1 |
| LRP6 | low density lipoprotein receptor-related protein 6 |
| MAP4K4 | mitogen-activated protein kinase kinase kinase kinase 4 |
| WNT3A | wingless-type MMTV integration site family, member 3A |
