behcet's disease Gene Set

Dataset GWASdb SNP-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://jjwanglab.org/gwasdb/gwasdb2/gwasdb2/go_trait/DOID:13241
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Genes

66 genes associated with the disease behcet's disease in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

Symbol Name Standardized Value
HLA-B major histocompatibility complex, class I, B 2.21116
PSORS1C1 psoriasis susceptibility 1 candidate 1 2.01898
IL10 interleukin 10 1.93435
CCHCR1 coiled-coil alpha-helical rod protein 1 1.74356
MICA MHC class I polypeptide-related sequence A 1.70897
MOG myelin oligodendrocyte glycoprotein 1.61458
ERAP1 endoplasmic reticulum aminopeptidase 1 1.59609
C6ORF15 chromosome 6 open reading frame 15 1.57645
ZNRD1-AS1 ZNRD1 antisense RNA 1 1.54582
HCP5 HLA complex P5 (non-protein coding) 1.54476
KLRC4 killer cell lectin-like receptor subfamily C, member 4 1.50906
STAT4 signal transducer and activator of transcription 4 1.50906
PSORS1C2 psoriasis susceptibility 1 candidate 2 1.46622
TFCP2L1 transcription factor CP2-like 1 1.45471
HLA-F-AS1 HLA-F antisense RNA 1 1.41484
MICB MHC class I polypeptide-related sequence B 1.366
DDR1 discoidin domain receptor tyrosine kinase 1 1.29681
DPCR1 diffuse panbronchiolitis critical region 1 1.28712
DDX39B DEAD (Asp-Glu-Ala-Asp) box polypeptide 39B 1.22784
LTA lymphotoxin alpha 1.15841
HCG18 HLA complex group 18 (non-protein coding) 1.15288
RNF175 ring finger protein 175 1.12853
TRIM26 tripartite motif containing 26 1.12155
NFKBIL1 nuclear factor of kappa light polypeptide gene enhancer in B-cells inhibitor-like 1 1.12017
FOXP1 forkhead box P1 1.06089
CLASP2 cytoplasmic linker associated protein 2 1.05771
ATP6V1G2 ATPase, H+ transporting, lysosomal 13kDa, V1 subunit G2 1.03421
VARS2 valyl-tRNA synthetase 2, mitochondrial 1.03155
ATP6V1G2-DDX39B ATP6V1G2-DDX39B readthrough (NMD candidate) 1.02545
CCDC180 coiled-coil domain containing 180 1.01984
ASTN2 astrotactin 2 1.01165
LACC1 laccase (multicopper oxidoreductase) domain containing 1 0.997473
HLA-F major histocompatibility complex, class I, F 0.994228
SFTA2 surfactant associated 2 0.992818
GPM6A glycoprotein M6A 0.947208
POU5F1 POU class 5 homeobox 1 0.943097
KLRK1 killer cell lectin-like receptor subfamily K, member 1 0.937304
CSMD1 CUB and Sushi multiple domains 1 0.93103
HCG27 HLA complex group 27 (non-protein coding) 0.921998
FBXL2 F-box and leucine-rich repeat protein 2 0.915252
MUC22 mucin 22 0.909246
DOCK4 dedicator of cytokinesis 4 0.895671
UBP1 upstream binding protein 1 (LBP-1a) 0.87287
NSMCE2 non-SMC element 2, MMS21 homolog (S. cerevisiae) 0.87232
MCF2L2 MCF.2 cell line derived transforming sequence-like 2 0.865959
DCC DCC netrin 1 receptor 0.859451
ZC3H13 zinc finger CCCH-type containing 13 0.851323
WDFY4 WDFY family member 4 0.842929
EFCAB11 EF-hand calcium binding domain 11 0.810532
PPP1R10 protein phosphatase 1, regulatory subunit 10 0.807706
MDC1 mediator of DNA-damage checkpoint 1 0.807358
JARID2 jumonji, AT rich interactive domain 2 0.796329
IL1R2 interleukin 1 receptor, type II 0.781646
WWTR1 WW domain containing transcription regulator 1 0.77375
CCDC42 coiled-coil domain containing 42 0.75112
LOC100287329 uncharacterized LOC100287329 0.723979
ACSBG1 acyl-CoA synthetase bubblegum family member 1 0.704419
FXYD5 FXYD domain containing ion transport regulator 5 0.703692
FYCO1 FYVE and coiled-coil domain containing 1 0.69739
ILDR1 immunoglobulin-like domain containing receptor 1 0.693888
CDHR3 cadherin-related family member 3 0.69066
CDSN corneodesmosin 0.682129
TCF19 transcription factor 19 0.670567
CPVL carboxypeptidase, vitellogenic-like 0.668836
UBAC2 UBA domain containing 2 0.547225
UBASH3B ubiquitin associated and SH3 domain containing B 0.51399