dry skin Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description Skin characterized by the lack of natural or normal moisture. (Human Phenotype Ontology, HP_0000958)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003853
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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