abnormal circadian regulation of heart rate Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description anomaly in the process in which an organism modulates its heart rate at different values with a regularity of approximately 24 hours (Mammalian Phenotype Ontology, MP_0011021)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0011021
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5 gene mutations causing the abnormal circadian regulation of heart rate phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ARNTL aryl hydrocarbon receptor nuclear translocator-like
CLOCK clock circadian regulator
NPY2R neuropeptide Y receptor Y2
PTGS1 prostaglandin-endoperoxide synthase 1 (prostaglandin G/H synthase and cyclooxygenase)
TPH2 tryptophan hydroxylase 2