abnormal circulating adrenaline level Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description aberrant 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_0005660)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0005660
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Genes

17 gene mutations causing the abnormal 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
CHGA chromogranin A
CRH corticotropin releasing hormone
DBH dopamine beta-hydroxylase (dopamine beta-monooxygenase)
EGLN3 egl-9 family hypoxia-inducible factor 3
FTO fat mass and obesity associated
MC2R melanocortin 2 receptor (adrenocorticotropic hormone)
NPAS2 neuronal PAS domain protein 2
NPPA natriuretic peptide A
NR3C1 nuclear receptor subfamily 3, group C, member 1 (glucocorticoid receptor)
POMC proopiomelanocortin
RIMS2 regulating synaptic membrane exocytosis 2
RNLS renalase, FAD-dependent amine oxidase
SLC6A2 solute carrier family 6 (neurotransmitter transporter), member 2
VAV2 vav 2 guanine nucleotide exchange factor
VAV3 vav 3 guanine nucleotide exchange factor