abnormal sympathetic nervous system physiology Gene Set
Genes
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
|