abnormal embryonic cloaca morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
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)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0010115
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7 gene mutations causing the abnormal embryonic cloaca morphology 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
EFNB2 ephrin-B2
FGF10 fibroblast growth factor 10
NOG noggin
TP63 tumor protein p63
WDPCP WD repeat containing planar cell polarity effector