decreased circulating adrenaline level Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description less than the normal concentration in the blood of a catecholamine hormone that stimulates the adrenergic receptors and that causes systemic vasoconstriction and gastrointestinal relaxation, stimulates the heart, and dilates bronchi and cerebral vessels (Mammalian Phenotype Ontology, MP_0005661)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0005661
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Genes

8 gene mutations causing the decreased circulating adrenaline level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ARNTL aryl hydrocarbon receptor nuclear translocator-like
ARRDC3 arrestin domain containing 3
CRH corticotropin releasing hormone
EGLN3 egl-9 family hypoxia-inducible factor 3
MC2R melanocortin 2 receptor (adrenocorticotropic hormone)
NPAS2 neuronal PAS domain protein 2
POMC proopiomelanocortin
RIMS2 regulating synaptic membrane exocytosis 2