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)
External Link	http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0001863
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Genes

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