abnormal circulating noradrenaline level Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description aberrant blood amount of the hormone secreted by the adrenal medulla and acts as a neurotransmitter in the sympathetic peripheral nervous system and in some tracts of the CNS; noradrenaline is the demethylated biosynthetic precursor of epinephrine (Mammalian Phenotype Ontology, MP_0005663)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0005663
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Genes

19 gene mutations causing the abnormal circulating noradrenaline level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ARNTL aryl hydrocarbon receptor nuclear translocator-like
BRAF B-Raf proto-oncogene, serine/threonine kinase
CHGA chromogranin A
CRH corticotropin releasing hormone
DBH dopamine beta-hydroxylase (dopamine beta-monooxygenase)
EGLN3 egl-9 family hypoxia-inducible factor 3
EPAS1 endothelial PAS domain protein 1
FFAR3 free fatty acid receptor 3
HTR1A 5-hydroxytryptamine (serotonin) receptor 1A, G protein-coupled
KL klotho
LY6E lymphocyte antigen 6 complex, locus E
NPAS2 neuronal PAS domain protein 2
NR3C1 nuclear receptor subfamily 3, group C, member 1 (glucocorticoid receptor)
PDC phosducin
RNLS renalase, FAD-dependent amine oxidase
SLC6A2 solute carrier family 6 (neurotransmitter transporter), member 2
SPR sepiapterin reductase (7,8-dihydrobiopterin:NADP+ oxidoreductase)
VAV2 vav 2 guanine nucleotide exchange factor
VAV3 vav 3 guanine nucleotide exchange factor