atopic dermatitis Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A dermatitis that is a chronically relapsing inflammatory allergic response located_in the skin that causes itching and flaking. (Human Disease Ontology, DOID_3310)
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19 genes associated with the disease atopic dermatitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
C11ORF30 chromosome 11 open reading frame 30
CCL5 chemokine (C-C motif) ligand 5
CMA1 chymase 1, mast cell
FLG filaggrin
IL12A interleukin 12A
IL12B interleukin 12B
IL12RB1 interleukin 12 receptor, beta 1
IL12RB2 interleukin 12 receptor, beta 2
IL13 interleukin 13
IL18 interleukin 18
IL4 interleukin 4
IL4R interleukin 4 receptor
IRF2 interferon regulatory factor 2
MS4A2 membrane-spanning 4-domains, subfamily A, member 2
NOD1 nucleotide-binding oligomerization domain containing 1
PHF11 PHD finger protein 11
SPINK5 serine peptidase inhibitor, Kazal type 5
TGFB1 transforming growth factor, beta 1
TLR2 toll-like receptor 2