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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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