ureteropelvic junction atresia Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description congenital absence or closure of the connection between the ureter and the renal pelvis (Mammalian Phenotype Ontology, MP_0011489)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0011489
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1 gene mutations causing the ureteropelvic junction atresia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AGTR2 angiotensin II receptor, type 2