Cellulitis Gene Set

Dataset HuGE Navigator Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description A skin disease where there is a diffuse infection of connective tissue with severe inflammation of dermal and subcutaneous layers of the skin. Cellulitis can be caused by normal skin flora or by exogenous bacteria, and often occurs where the skin has previously been broken: cracks in the skin, cuts, blisters, burns, insect bites, surgical wounds, or sites of intravenous catheter insertion. (Human Disease Ontology, DOID_3488)
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Genes

15 genes associated with the Cellulitis phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Symbol Name
ACE angiotensin I converting enzyme
ADIPOQ adiponectin, C1Q and collagen domain containing
ADIPOR1 adiponectin receptor 1
APOE apolipoprotein E
CETP cholesteryl ester transfer protein, plasma
ESR1 estrogen receptor 1
ESR2 estrogen receptor 2 (ER beta)
HIF1A hypoxia inducible factor 1, alpha subunit (basic helix-loop-helix transcription factor)
IL1A interleukin 1, alpha
LDLR low density lipoprotein receptor
NOS3 nitric oxide synthase 3 (endothelial cell)
PPARG peroxisome proliferator-activated receptor gamma
TGFB1 transforming growth factor, beta 1
TGFB2 transforming growth factor, beta 2
TLR4 toll-like receptor 4