double ureter Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description A developmental anomaly characterized by the presence of two, instead of one, ureter connecting a kidney to the bladder. (Human Phenotype Ontology, HP_0000073)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0011493
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Genes

4 gene mutations causing the double ureter phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AGTR2 angiotensin II receptor, type 2
LZTS2 leucine zipper, putative tumor suppressor 2
NFIA nuclear factor I/A
PAX2 paired box 2