delayed circadian phase Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description decrease in the phase relationship between a temporal synchronizing event (such as light cycle) and a phase reference point of an animal (such as activity onset) (Mammalian Phenotype Ontology, MP_0002565)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0002565
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Genes

9 gene mutations causing the delayed circadian phase phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ADCYAP1R1 adenylate cyclase activating polypeptide 1 (pituitary) receptor type I
ARNTL aryl hydrocarbon receptor nuclear translocator-like
BHLHE40 basic helix-loop-helix family, member e40
BHLHE41 basic helix-loop-helix family, member e41
CRX cone-rod homeobox
NAGLU N-acetylglucosaminidase, alpha
NGB neuroglobin
PHLPP1 PH domain and leucine rich repeat protein phosphatase 1
USP2 ubiquitin specific peptidase 2