persistent cloaca Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description Developmental anomaly in which the vagina, bladder, and rectum fuse resulting in a common channel. (Human Phenotype Ontology, HP_0012621)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003129
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Genes

2 gene mutations causing the persistent cloaca phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
EFNB2 ephrin-B2
SALL4 spalt-like transcription factor 4