abnormal autonomic nervous system physiology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description A functional abnormality of the autonomic nervous system. (Human Phenotype Ontology, HP_0012332)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0006276
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Genes

33 gene mutations causing the abnormal autonomic 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
CHRNA3 cholinergic receptor, nicotinic, alpha 3 (neuronal)
CYP19A1 cytochrome P450, family 19, subfamily A, polypeptide 1
DBX1 developing brain homeobox 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
KDM6B lysine (K)-specific demethylase 6B
LEP leptin
MAGED1 melanoma antigen family D1
NDN necdin, melanoma antigen (MAGE) family member
NDUFS4 NADH dehydrogenase (ubiquinone) Fe-S protein 4, 18kDa (NADH-coenzyme Q reductase)
NHLH1 nescient helix loop helix 1
NTRK1 neurotrophic tyrosine kinase, receptor, type 1
OXT oxytocin/neurophysin I prepropeptide
PIRT phosphoinositide-interacting regulator of transient receptor potential channels
POU4F3 POU class 4 homeobox 3
PRKAA2 protein kinase, AMP-activated, alpha 2 catalytic subunit
PRLH prolactin releasing hormone
REN renin
ROBO3 roundabout, axon guidance receptor, homolog 3 (Drosophila)
SLC17A6 solute carrier family 17 (vesicular glutamate transporter), member 6
TPH2 tryptophan hydroxylase 2
VAV3 vav 3 guanine nucleotide exchange factor