vascular stenosis Gene Set

Dataset	MPO Gene-Phenotype Associations
Category	disease or phenotype associations
Type	phenotype
Description	a stricture or occlusion of a lumen of vascular tissue (Mammalian Phenotype Ontology, MP_0005412)
External Link	http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0005412
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Genes

25 gene mutations causing the vascular stenosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol	Name
ABCC9	ATP-binding cassette, sub-family C (CFTR/MRP), member 9
ADIPOQ	adiponectin, C1Q and collagen domain containing
APLN	apelin
APOE	apolipoprotein E
CCM2	cerebral cavernous malformation 2
CITED2	Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2
CXCR4	chemokine (C-X-C motif) receptor 4
DLL1	delta-like 1 (Drosophila)
DLL4	delta-like 4 (Drosophila)
DNAI1	dynein, axonemal, intermediate chain 1
EFEMP2	EGF containing fibulin-like extracellular matrix protein 2
ELN	elastin
GATA4	GATA binding protein 4
GATA5	GATA binding protein 5
GPER1	G protein-coupled estrogen receptor 1
HEY2	hes-related family bHLH transcription factor with YRPW motif 2
IL1RN	interleukin 1 receptor antagonist
LOX	lysyl oxidase
PSEN1	presenilin 1
PTGIR	prostaglandin I2 (prostacyclin) receptor (IP)
RRAS	related RAS viral (r-ras) oncogene homolog
RXRA	retinoid X receptor, alpha
SGCB	sarcoglycan, beta (43kDa dystrophin-associated glycoprotein)
SGCD	sarcoglycan, delta (35kDa dystrophin-associated glycoprotein)
ZFPM2	zinc finger protein, FOG family member 2