abnormal circadian phase Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description anomaly 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_0002561)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0002561
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26 gene mutations causing the abnormal circadian phase phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ADCYAP1 adenylate cyclase activating polypeptide 1 (pituitary)
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
CLOCK clock circadian regulator
CREB1 cAMP responsive element binding protein 1
CRX cone-rod homeobox
ID2 inhibitor of DNA binding 2, dominant negative helix-loop-helix protein
MC4R melanocortin 4 receptor
MTNR1A melatonin receptor 1A
NAGLU N-acetylglucosaminidase, alpha
NCAM1 neural cell adhesion molecule 1
NGB neuroglobin
NR1D1 nuclear receptor subfamily 1, group D, member 1
OPN4 opsin 4
PER1 period circadian clock 1
PER2 period circadian clock 2
PHLPP1 PH domain and leucine rich repeat protein phosphatase 1
POU4F2 POU class 4 homeobox 2
PROKR2 prokineticin receptor 2
RASD1 RAS, dexamethasone-induced 1
RAX retina and anterior neural fold homeobox
SYT10 synaptotagmin X
USP2 ubiquitin specific peptidase 2
VIP vasoactive intestinal peptide