decreased vasoconstriction Gene Set
Genes
17 gene mutations causing the decreased vasoconstriction phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
| Symbol |
Name |
|
ACTA2
|
actin, alpha 2, smooth muscle, aorta
|
|
ADRA1A
|
adrenoceptor alpha 1A
|
|
ADRA1B
|
adrenoceptor alpha 1B
|
|
APEX1
|
APEX nuclease (multifunctional DNA repair enzyme) 1
|
|
ARHGEF12
|
Rho guanine nucleotide exchange factor (GEF) 12
|
|
ASIC2
|
acid sensing (proton gated) ion channel 2
|
|
ATP2B4
|
ATPase, Ca++ transporting, plasma membrane 4
|
|
CAV1
|
caveolin 1, caveolae protein, 22kDa
|
|
FGF2
|
fibroblast growth factor 2 (basic)
|
|
IL10
|
interleukin 10
|
|
KCNA5
|
potassium channel, voltage gated shaker related subfamily A, member 5
|
|
MYH11
|
myosin, heavy chain 11, smooth muscle
|
|
NCF1
|
neutrophil cytosolic factor 1
|
|
P2RY6
|
pyrimidinergic receptor P2Y, G-protein coupled, 6
|
|
REN
|
renin
|
|
SMTN
|
smoothelin
|
|
SMTNL1
|
smoothelin-like 1
|
