behcet syndrome; Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A vasculitis that is characterized by an autoimmune mediated inflammation of the blood vessels throughout the body leading to ulcerations on the mouth and sometimes the genitals, notorious for causing hypopyon uveitis. (Human Disease Ontology, DOID_13241)
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Genes

23 genes associated with the disease behcet syndrome; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
CCL2 chemokine (C-C motif) ligand 2
CTLA4 cytotoxic T-lymphocyte-associated protein 4
CXCL8 chemokine (C-X-C motif) ligand 8
HLA-A major histocompatibility complex, class I, A
HLA-B major histocompatibility complex, class I, B
HLA-C major histocompatibility complex, class I, C
HLA-DQB1 major histocompatibility complex, class II, DQ beta 1
HLA-DRB1 major histocompatibility complex, class II, DR beta 1
IFNG interferon, gamma
IL10 interleukin 10
IL17F interleukin 17F
IL6 interleukin 6
IL6R interleukin 6 receptor
MEFV Mediterranean fever
NFKB1 nuclear factor of kappa light polypeptide gene enhancer in B-cells 1
NOD2 nucleotide-binding oligomerization domain containing 2
SLC11A1 solute carrier family 11 (proton-coupled divalent metal ion transporter), member 1
SUMO4 small ubiquitin-like modifier 4
TGFB1 transforming growth factor, beta 1
TGFBR1 transforming growth factor, beta receptor 1
TLR2 toll-like receptor 2
TNF tumor necrosis factor
VEGFA vascular endothelial growth factor A