|Dataset||MPO Gene-Phenotype Associations|
|Category||disease or phenotype associations|
|Description||any structural anomaly of the endoderm-lined chamber that develops as pouch-like dilation of the caudal end of the hindgut and receives the allantois ventrally and two mesonephric ducts laterally; caudally it ends blindly at the cloacal membrane formed by the union of proctodeal (anal pit) ectoderm and cloacal endoderm, with no intervening mesoderm (Mammalian Phenotype Ontology, MP_0010115)|
|Downloads & Tools|
7 gene mutations causing the abnormal embryonic cloaca morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.