abnormal urine prostaglandin level Gene Set

Dataset	MPO Gene-Phenotype Associations
Category	disease or phenotype associations
Type	phenotype
Description	any change in the urinary amount of any of a class of mediators with effects of vasodilation, vasoconstriction, and smooth muscle stimulation (Mammalian Phenotype Ontology, MP_0011562)
External Link	http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0011562
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Genes

4 gene mutations causing the abnormal urine prostaglandin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol	Name
NOS2	nitric oxide synthase 2, inducible
PTGS1	prostaglandin-endoperoxide synthase 1 (prostaglandin G/H synthase and cyclooxygenase)
PTGS2	prostaglandin-endoperoxide synthase 2 (prostaglandin G/H synthase and cyclooxygenase)
SLC12A1	solute carrier family 12 (sodium/potassium/chloride transporter), member 1