increased vascular permeability Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description greater or faster ability of the blood vessels to permit the passage of substances such as fluid, heat, or gases (Mammalian Phenotype Ontology, MP_0003070)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003070
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Genes

33 gene mutations causing the increased vascular permeability phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ACTA2 actin, alpha 2, smooth muscle, aorta
ADORA2B adenosine A2b receptor
ANGPTL4 angiopoietin-like 4
ANKRD17 ankyrin repeat domain 17
AXL AXL receptor tyrosine kinase
C1QTNF5 C1q and tumor necrosis factor related protein 5
CAV1 caveolin 1, caveolae protein, 22kDa
CBS cystathionine-beta-synthase
CRIM1 cysteine rich transmembrane BMP regulator 1 (chordin-like)
CTTN cortactin
GAS6 growth arrest-specific 6
GATA2 GATA binding protein 2
GPR17 G protein-coupled receptor 17
GSN gelsolin
ID1 inhibitor of DNA binding 1, dominant negative helix-loop-helix protein
INS insulin
KRT1 keratin 1, type II
LRP5 low density lipoprotein receptor-related protein 5
MED1 mediator complex subunit 1
MMP9 matrix metallopeptidase 9
NDP Norrie disease (pseudoglioma)
NGF nerve growth factor (beta polypeptide)
NR1H3 nuclear receptor subfamily 1, group H, member 3
NT5E 5'-nucleotidase, ecto (CD73)
PECAM1 platelet/endothelial cell adhesion molecule 1
PLAC8 placenta-specific 8
PLVAP plasmalemma vesicle associated protein
PROS1 protein S (alpha)
RAMP2 receptor (G protein-coupled) activity modifying protein 2
SERPING1 serpin peptidase inhibitor, clade G (C1 inhibitor), member 1
TIMP1 TIMP metallopeptidase inhibitor 1
TRPM4 transient receptor potential cation channel, subfamily M, member 4
VLDLR very low density lipoprotein receptor