abnormal blood pressure regulation Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any anomaly in the process that modulates the force with which blood travels through the circulatory system, which is controlled by a balance of processes that increase pressure and decrease pressure (Mammalian Phenotype Ontology, MP_0010695)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0010695
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8 gene mutations causing the abnormal blood pressure regulation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ARNTL aryl hydrocarbon receptor nuclear translocator-like
CD36 CD36 molecule (thrombospondin receptor)
CLOCK clock circadian regulator
F2R coagulation factor II (thrombin) receptor
KLF3 Kruppel-like factor 3 (basic)
PDLIM5 PDZ and LIM domain 5
PTGS1 prostaglandin-endoperoxide synthase 1 (prostaglandin G/H synthase and cyclooxygenase)
TPH2 tryptophan hydroxylase 2