vasculitis Gene Set

Dataset GWASdb SNP-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description A vascular disease that is characterized by inflammation of the blood vessels. (Human Disease Ontology, DOID_865)
External Link http://jjwanglab.org/gwasdb/gwasdb2/gwasdb2/go_trait/HP:0002633
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Genes

16 genes associated with the vasculitis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

Symbol Name Standardized Value
HLA-DPB2 major histocompatibility complex, class II, DP beta 2 (pseudogene) 2.08024
F8 coagulation factor VIII, procoagulant component 1.09906
TSC22D1 TSC22 domain family, member 1 0.969142
WNT9B wingless-type MMTV integration site family, member 9B 0.855449
NTN4 netrin 4 0.842167
TMEM164 transmembrane protein 164 0.836232
CTLA4 cytotoxic T-lymphocyte-associated protein 4 0.81905
PRR27 proline rich 27 0.80501
NOX4 NADPH oxidase 4 0.798387
NLGN4X neuroligin 4, X-linked 0.72096
NELL1 NEL-like 1 (chicken) 0.704251
MAMLD1 mastermind-like domain containing 1 0.667695
DAB1 Dab, reelin signal transducer, homolog 1 (Drosophila) 0.642942
MPDZ multiple PDZ domain protein 0.609048
FGF12 fibroblast growth factor 12 0.467126
VWF von Willebrand factor 0.451714