vascular inflammation Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description local accumulation of fluid, plasma proteins, and leukocytes in a blood vessel (Mammalian Phenotype Ontology, MP_0001863)
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24 gene mutations causing the vascular inflammation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ADM adrenomedullin
APOE apolipoprotein E
BCL2L11 BCL2-like 11 (apoptosis facilitator)
CHD2 chromodomain helicase DNA binding protein 2
CTLA4 cytotoxic T-lymphocyte-associated protein 4
FAS Fas cell surface death receptor
FBN1 fibrillin 1
FCGR2B Fc fragment of IgG, low affinity IIb, receptor (CD32)
GPX7 glutathione peroxidase 7
IFNGR1 interferon gamma receptor 1
IL1RN interleukin 1 receptor antagonist
IL2 interleukin 2
KLF15 Kruppel-like factor 15
MTAP methylthioadenosine phosphorylase
PIP prolactin-induced protein
PTPN22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid)
SSBP2 single-stranded DNA binding protein 2
TGFB1 transforming growth factor, beta 1
TIMP3 TIMP metallopeptidase inhibitor 3
TK1 thymidine kinase 1, soluble
TNIP1 TNFAIP3 interacting protein 1
TP53 tumor protein p53
TUSC2 tumor suppressor candidate 2
ZFP36 ZFP36 ring finger protein