abnormal adrenaline level Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description aberrant concentration in the blood or tissues of this 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_0003962)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003962
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Genes

27 gene mutations causing the abnormal adrenaline level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ADCYAP1 adenylate cyclase activating polypeptide 1 (pituitary)
ADIPOQ adiponectin, C1Q and collagen domain containing
AGTR2 angiotensin II receptor, type 2
ARNTL aryl hydrocarbon receptor nuclear translocator-like
ARRDC3 arrestin domain containing 3
CHGA chromogranin A
CHGB chromogranin B
CRH corticotropin releasing hormone
CYP11A1 cytochrome P450, family 11, subfamily A, polypeptide 1
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)
MRAP2 melanocortin 2 receptor accessory protein 2
NPAS2 neuronal PAS domain protein 2
NPPA natriuretic peptide A
NR3C1 nuclear receptor subfamily 3, group C, member 1 (glucocorticoid receptor)
PNMT phenylethanolamine N-methyltransferase
POMC proopiomelanocortin
RIMS2 regulating synaptic membrane exocytosis 2
RNLS renalase, FAD-dependent amine oxidase
SLC23A2 solute carrier family 23 (ascorbic acid transporter), member 2
SLC6A2 solute carrier family 6 (neurotransmitter transporter), member 2
TH tyrosine hydroxylase
UBE3A ubiquitin protein ligase E3A
VAV2 vav 2 guanine nucleotide exchange factor
VAV3 vav 3 guanine nucleotide exchange factor
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