abnormal systemic arterial blood pressure regulation Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description anomaly in the process that modulates the force with which blood travels through the systemic arterial circulatory system (Mammalian Phenotype Ontology, MP_0010697)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0010697
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5 gene mutations causing the abnormal systemic arterial blood pressure regulation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ARNTL aryl hydrocarbon receptor nuclear translocator-like
CLOCK clock circadian regulator
F2R coagulation factor II (thrombin) receptor
PTGS1 prostaglandin-endoperoxide synthase 1 (prostaglandin G/H synthase and cyclooxygenase)
TPH2 tryptophan hydroxylase 2