hypoxia Gene Set
Genes
27 gene mutations causing the hypoxia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
| Symbol |
Name |
|
ATF2
|
activating transcription factor 2
|
|
COMT
|
catechol-O-methyltransferase
|
|
DHCR7
|
7-dehydrocholesterol reductase
|
|
EDN1
|
endothelin 1
|
|
EDN2
|
endothelin 2
|
|
EDNRB
|
endothelin receptor type B
|
|
EGFL7
|
EGF-like-domain, multiple 7
|
|
EPO
|
erythropoietin
|
|
FGF9
|
fibroblast growth factor 9
|
|
FOSL2
|
FOS-like antigen 2
|
|
GAD1
|
glutamate decarboxylase 1 (brain, 67kDa)
|
|
GRID2
|
glutamate receptor, ionotropic, delta 2
|
|
GSX2
|
GS homeobox 2
|
|
HIF1A
|
hypoxia inducible factor 1, alpha subunit (basic helix-loop-helix transcription factor)
|
|
HMOX2
|
heme oxygenase 2
|
|
LAMA4
|
laminin, alpha 4
|
|
LIF
|
leukemia inhibitory factor
|
|
MB
|
myoglobin
|
|
NDN
|
necdin, melanoma antigen (MAGE) family member
|
|
PFKM
|
phosphofructokinase, muscle
|
|
RB1
|
retinoblastoma 1
|
|
SCN2A
|
sodium channel, voltage gated, type II alpha subunit
|
|
TAL1
|
T-cell acute lymphocytic leukemia 1
|
|
TFRC
|
transferrin receptor
|
|
TMEM38B
|
transmembrane protein 38B
|
|
TTN
|
titin
|
|
XDH
|
xanthine dehydrogenase
|
