increased angiogenesis Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description enhanced process of blood vessel formation and the subsequent remodeling process; does not refer to the initial establishment of the vascular network (Mammalian Phenotype Ontology, MP_0005601)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0005601
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Genes

22 gene mutations causing the increased angiogenesis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
A4GNT alpha-1,4-N-acetylglucosaminyltransferase
ADAMTS12 ADAM metallopeptidase with thrombospondin type 1 motif, 12
AGTR2 angiotensin II receptor, type 2
CRHR2 corticotropin releasing hormone receptor 2
DSTN destrin (actin depolymerizing factor)
FLT1 fms-related tyrosine kinase 1
HPSE heparanase
ITGB3 integrin, beta 3 (platelet glycoprotein IIIa, antigen CD61)
MB myoglobin
MED1 mediator complex subunit 1
MMP9 matrix metallopeptidase 9
NOTCH1 notch 1
PARVA parvin, alpha
PLXND1 plexin D1
RORA RAR-related orphan receptor A
S1PR2 sphingosine-1-phosphate receptor 2
SERPINE1 serpin peptidase inhibitor, clade E (nexin, plasminogen activator inhibitor type 1), member 1
SERPINF1 serpin peptidase inhibitor, clade F (alpha-2 antiplasmin, pigment epithelium derived factor), member 1
STARD13 StAR-related lipid transfer (START) domain containing 13
TP53 tumor protein p53
VASH1 vasohibin 1
VHL von Hippel-Lindau tumor suppressor, E3 ubiquitin protein ligase