dry skin Gene Set
Genes
17 gene mutations causing the dry skin phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
| Symbol |
Name |
|
ALOX12B
|
arachidonate 12-lipoxygenase, 12R type
|
|
AQP2
|
aquaporin 2 (collecting duct)
|
|
AVPR2
|
arginine vasopressin receptor 2
|
|
CYP7A1
|
cytochrome P450, family 7, subfamily A, polypeptide 1
|
|
DGAT2
|
diacylglycerol O-acyltransferase 2
|
|
FLG
|
filaggrin
|
|
FOXP3
|
forkhead box P3
|
|
GBA
|
glucosidase, beta, acid
|
|
HAP1
|
huntingtin-associated protein 1
|
|
LBR
|
lamin B receptor
|
|
MIR205
|
microRNA 205
|
|
NFKBIA
|
nuclear factor of kappa light polypeptide gene enhancer in B-cells inhibitor, alpha
|
|
PCCA
|
propionyl CoA carboxylase, alpha polypeptide
|
|
PRSS8
|
protease, serine, 8
|
|
SCD
|
stearoyl-CoA desaturase (delta-9-desaturase)
|
|
ST14
|
suppression of tumorigenicity 14 (colon carcinoma)
|
|
TRPV3
|
transient receptor potential cation channel, subfamily V, member 3
|
