atopic dermatitis Gene Set

Dataset DISEASES Experimental Gene-Disease Assocation Evidence Scores
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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20 genes associated with the disease atopic dermatitis in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
OR10A3 olfactory receptor, family 10, subfamily A, member 3 1.46288
GLB1 galactosidase, beta 1 1.41058
ZNF365 zinc finger protein 365 1.34736
CCDC80 coiled-coil domain containing 80 1.32252
IL18R1 interleukin 18 receptor 1 1.24793
HLA-C major histocompatibility complex, class I, C 1.24299
OVOL1 ovo-like zinc finger 1 0.965481
FLG filaggrin 0.835734
C11ORF30 chromosome 11 open reading frame 30 0.641775
ACTL9 actin-like 9 0.544585
CYP24A1 cytochrome P450, family 24, subfamily A, polypeptide 1 0.486425
KIF3A kinesin family member 3A 0.449873
ADO 2-aminoethanethiol (cysteamine) dioxygenase 0.368757
BCL2L11 BCL2-like 11 (apoptosis facilitator) 0.345945
RNASEH2C ribonuclease H2, subunit C 0.297866
IL13 interleukin 13 0.197766
DDX39B DEAD (Asp-Glu-Ala-Asp) box polypeptide 39B 0.197766
LRRC32 leucine rich repeat containing 32 0.15771
NCF4 neutrophil cytosolic factor 4, 40kDa 0.080593
CLEC16A C-type lectin domain family 16, member A 0.080593