Angioedema Gene Set

Dataset HuGE Navigator Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description A skin disease characterized by the rapid swelling of the dermis, subcutaneous tissue, mucosa and submucosal tissues. (Human Disease Ontology, DOID_1558)
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17 genes associated with the Angioedema phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Symbol Name
ABI3BP ABI family, member 3 (NESH) binding protein
ACE angiotensin I converting enzyme
BDKRB2 bradykinin receptor B2
BICC1 BicC family RNA binding protein 1
COL24A1 collagen, type XXIV, alpha 1
ETV6 ets variant 6
F12 coagulation factor XII (Hageman factor)
FBXL7 F-box and leucine-rich repeat protein 7
GALNT3 polypeptide N-acetylgalactosaminyltransferase 3
HLF hepatic leukemia factor
MME membrane metallo-endopeptidase
PRKCQ protein kinase C, theta
RAD51B RAD51 paralog B
RIMS1 regulating synaptic membrane exocytosis 1
TGFB1 transforming growth factor, beta 1
TP53 tumor protein p53
XPNPEP2 X-prolyl aminopeptidase (aminopeptidase P) 2, membrane-bound