erythema Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Redness of the skin, caused by hyperemia of the capillaries in the lower layers of the skin. (Human Phenotype Ontology, HP_0010783)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0010783
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Genes

24 genes associated with the erythema phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ADAM17 ADAM metallopeptidase domain 17
AIP aryl hydrocarbon receptor interacting protein
AP1S1 adaptor-related protein complex 1, sigma 1 subunit
ATP2C1 ATPase, Ca++ transporting, type 2C, member 1
CDSN corneodesmosin
DSG4 desmoglein 4
ELOVL4 ELOVL fatty acid elongase 4
FECH ferrochelatase
GJB3 gap junction protein, beta 3, 31kDa
GJB4 gap junction protein, beta 4, 30.3kDa
IKBKG inhibitor of kappa light polypeptide gene enhancer in B-cells, kinase gamma
IL36RN interleukin 36 receptor antagonist
KIT v-kit Hardy-Zuckerman 4 feline sarcoma viral oncogene homolog
KRT1 keratin 1, type II
KRT10 keratin 10, type I
MBTPS2 membrane-bound transcription factor peptidase, site 2
PLCG2 phospholipase C, gamma 2 (phosphatidylinositol-specific)
PSMB8 proteasome (prosome, macropain) subunit, beta type, 8
SAT1 spermidine/spermine N1-acetyltransferase 1
SERPING1 serpin peptidase inhibitor, clade G (C1 inhibitor), member 1
SLURP1 secreted LY6/PLAUR domain containing 1
TGM5 transglutaminase 5
TMEM173 transmembrane protein 173
WNT10A wingless-type MMTV integration site family, member 10A