Skin Ulcer Gene Set

Dataset HuGE Navigator Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description A discontinuity of the skin exhibiting complete loss of the epidermis and often portions of the dermis and even subcutaneous fat. (Human Phenotype Ontology, HP_0200042)
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Genes

20 genes associated with the Skin Ulcer phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Symbol Name
BRAF B-Raf proto-oncogene, serine/threonine kinase
CXCL12 chemokine (C-X-C motif) ligand 12
HLA-B major histocompatibility complex, class I, B
IFNG interferon, gamma
IL10 interleukin 10
IL12A interleukin 12A
IL1A interleukin 1, alpha
IL1B interleukin 1, beta
IL1R1 interleukin 1 receptor, type I
IL1RN interleukin 1 receptor antagonist
IL2 interleukin 2
IL4 interleukin 4
IL4R interleukin 4 receptor
IL6 interleukin 6
NRAS neuroblastoma RAS viral (v-ras) oncogene homolog
SLC11A1 solute carrier family 11 (proton-coupled divalent metal ion transporter), member 1
SLC6A4 solute carrier family 6 (neurotransmitter transporter), member 4
TGFB1 transforming growth factor, beta 1
TIMP1 TIMP metallopeptidase inhibitor 1
TNF tumor necrosis factor