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