abnormal circadian persistence Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description anomaly in the ability for an animal to retain a circadian rhythm when time cues are removed (Mammalian Phenotype Ontology, MP_0002559)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0002559
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9 gene mutations causing the abnormal circadian persistence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ARNTL aryl hydrocarbon receptor nuclear translocator-like
CLOCK clock circadian regulator
CRY2 cryptochrome circadian clock 2
ID2 inhibitor of DNA binding 2, dominant negative helix-loop-helix protein
PER1 period circadian clock 1
PER2 period circadian clock 2
PROKR2 prokineticin receptor 2
VIP vasoactive intestinal peptide
VIPR2 vasoactive intestinal peptide receptor 2