abnormal sympathetic nervous system physiology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any functional anomaly of the part of the autonomic nervous system that innervates smooth muscle, cardiac muscle and glands and mediates the body's response to stressful situations (Mammalian Phenotype Ontology, MP_0004183)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004183
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22 gene mutations causing the abnormal sympathetic nervous system physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ACHE acetylcholinesterase (Yt blood group)
ADRA1B adrenoceptor alpha 1B
AGTR2 angiotensin II receptor, type 2
AKAP10 A kinase (PRKA) anchor protein 10
ARL6 ADP-ribosylation factor-like 6
AVPR1A arginine vasopressin receptor 1A
CACNA1B calcium channel, voltage-dependent, N type, alpha 1B subunit
CALCB calcitonin-related polypeptide beta
CYP19A1 cytochrome P450, family 19, subfamily A, polypeptide 1
DRD5 dopamine receptor D5
EDN1 endothelin 1
FFAR3 free fatty acid receptor 3
FGF2 fibroblast growth factor 2 (basic)
GPSM1 G-protein signaling modulator 1
LEP leptin
MAGED1 melanoma antigen family D1
NTRK1 neurotrophic tyrosine kinase, receptor, type 1
OXT oxytocin/neurophysin I prepropeptide
PIRT phosphoinositide-interacting regulator of transient receptor potential channels
PRKAA2 protein kinase, AMP-activated, alpha 2 catalytic subunit
REN renin
VAV3 vav 3 guanine nucleotide exchange factor