Behcet Syndrome Gene Set

Dataset CTD 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)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D001528
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Genes

20 genes/proteins associated with the disease Behcet Syndrome from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
ITGAL integrin, alpha L (antigen CD11A (p180), lymphocyte function-associated antigen 1; alpha polypeptide) 2.88009
CCR1 chemokine (C-C motif) receptor 1 2.88009
KLRC4 killer cell lectin-like receptor subfamily C, member 4 2.88009
SERPINE1 serpin peptidase inhibitor, clade E (nexin, plasminogen activator inhibitor type 1), member 1 2.88009
CAT catalase 2.88009
CXCL8 chemokine (C-X-C motif) ligand 8 2.88009
APOA1 apolipoprotein A-I 2.88009
ICAM1 intercellular adhesion molecule 1 2.88009
ERAP1 endoplasmic reticulum aminopeptidase 1 2.88009
PSORS1C1 psoriasis susceptibility 1 candidate 1 2.88009
HLA-B major histocompatibility complex, class I, B 2.88009
ITGB2 integrin, beta 2 (complement component 3 receptor 3 and 4 subunit) 2.88009
STAT4 signal transducer and activator of transcription 4 2.88009
IL10 interleukin 10 2.88009
APOB apolipoprotein B 2.88009
MUCL1 mucin-like 1 1.2818
ABCB1 ATP-binding cassette, sub-family B (MDR/TAP), member 1 1.11501
LTF lactotransferrin 1.08619
IL4 interleukin 4 1.03493
TNF tumor necrosis factor 1.03382