Psoriasis Gene Set

Dataset GWAS Catalog SNP-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description A skin abnormality characterized by redness and irritation, with thick, red skin that displays flaky, silver-white patches (scales). (Human Phenotype Ontology, HP_0003765)
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17 genes associated with the Psoriasis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Symbol Name Standardized Value
HCP5 HLA complex P5 (non-protein coding) 1.20529
IL12B interleukin 12B 1.19997
LOC285626 uncharacterized LOC285626 1.06007
REV3L REV3-like, polymerase (DNA directed), zeta, catalytic subunit 1.03493
IL13 interleukin 13 0.831366
KCNH7 potassium channel, voltage gated eag related subfamily H, member 7 0.765464
TNFAIP3 tumor necrosis factor, alpha-induced protein 3 0.658916
NOS2 nitric oxide synthase 2, inducible 0.618573
TYK2 tyrosine kinase 2 0.618573
FBXL19 F-box and leucine-rich repeat protein 19 0.526478
STAT2 signal transducer and activator of transcription 2, 113kDa 0.522843
LINC01185 long intergenic non-protein coding RNA 1185 0.472799
SPATA2 spermatogenesis associated 2 0.434785
KIAA0391 KIAA0391 0.405958
IL23R interleukin 23 receptor 0.389385
COG6 component of oligomeric golgi complex 6 0.165905
TSC1 tuberous sclerosis 1 0.070053