urticaria Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Urticaria is a kind of skin rash notable for pale red, raised, itchy bumps that might also cause a burning or stinging sensation. It is often but not necessarily caused by an allergic reaction. (Experimental Factor Ontology, EFO_0005531)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0001025
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Genes

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

Symbol Name
ALAS2 5'-aminolevulinate synthase 2
ALDH3A2 aldehyde dehydrogenase 3 family, member A2
ANTXR2 anthrax toxin receptor 2
CASP10 caspase 10, apoptosis-related cysteine peptidase
CBS cystathionine-beta-synthase
CYBA cytochrome b-245, alpha polypeptide
CYBB cytochrome b-245, beta polypeptide
ELOVL4 ELOVL fatty acid elongase 4
FAS Fas cell surface death receptor
FASLG Fas ligand (TNF superfamily, member 6)
FECH ferrochelatase
FERMT1 fermitin family member 1
GJB2 gap junction protein, beta 2, 26kDa
GJB6 gap junction protein, beta 6, 30kDa
HLA-DQB1 major histocompatibility complex, class II, DQ beta 1
HLA-DRB1 major histocompatibility complex, class II, DR beta 1
KIT v-kit Hardy-Zuckerman 4 feline sarcoma viral oncogene homolog
MBTPS2 membrane-bound transcription factor peptidase, site 2
MVK mevalonate kinase
MYD88 myeloid differentiation primary response 88
NCF1 neutrophil cytosolic factor 1
NCF2 neutrophil cytosolic factor 2
NCF4 neutrophil cytosolic factor 4, 40kDa
NLRP12 NLR family, pyrin domain containing 12
NLRP3 NLR family, pyrin domain containing 3
PDGFRA platelet-derived growth factor receptor, alpha polypeptide
PIGT phosphatidylinositol glycan anchor biosynthesis, class T
SDHB succinate dehydrogenase complex, subunit B, iron sulfur (Ip)
SDHC succinate dehydrogenase complex, subunit C, integral membrane protein, 15kDa
SF3B4 splicing factor 3b, subunit 4, 49kDa
SPINK5 serine peptidase inhibitor, Kazal type 5
WAS Wiskott-Aldrich syndrome
WIPF1 WAS/WASL interacting protein family, member 1
WNT10A wingless-type MMTV integration site family, member 10A