abnormal physiological neovascularization Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description anomalies in the development of new blood vessels in restoration of blood circulation during the healing process (Mammalian Phenotype Ontology, MP_0003710)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003710
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18 gene mutations causing the abnormal physiological neovascularization phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
B4GALT1 UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1
CCL13 chemokine (C-C motif) ligand 13
CD44 CD44 molecule (Indian blood group)
CD47 CD47 molecule
CLIC4 chloride intracellular channel 4
CXCL12 chemokine (C-X-C motif) ligand 12
CXCR3 chemokine (C-X-C motif) receptor 3
EPAS1 endothelial PAS domain protein 1
FLT1 fms-related tyrosine kinase 1
H2AFX H2A histone family, member X
ITGB3 integrin, beta 3 (platelet glycoprotein IIIa, antigen CD61)
MFGE8 milk fat globule-EGF factor 8 protein
MMP9 matrix metallopeptidase 9
NOS2 nitric oxide synthase 2, inducible
PTK2B protein tyrosine kinase 2 beta
RRAS related RAS viral (r-ras) oncogene homolog
SPP1 secreted phosphoprotein 1
THBS1 thrombospondin 1