abnormal induced retinal neovascularization Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any anomaly in the response to conditions which induce the pathological growth of vessels into the retina (Mammalian Phenotype Ontology, MP_0009660)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0009660
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Genes

18 gene mutations causing the abnormal induced retinal neovascularization phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ADAM15 ADAM metallopeptidase domain 15
ANGPTL4 angiopoietin-like 4
BCL2 B-cell CLL/lymphoma 2
BMPER BMP binding endothelial regulator
DLL4 delta-like 4 (Drosophila)
F3 coagulation factor III (thromboplastin, tissue factor)
ITGB3 integrin, beta 3 (platelet glycoprotein IIIa, antigen CD61)
LIF leukemia inhibitory factor
MMP2 matrix metallopeptidase 2
MMP7 matrix metallopeptidase 7
MMP9 matrix metallopeptidase 9
NOS2 nitric oxide synthase 2, inducible
NOS3 nitric oxide synthase 3 (endothelial cell)
NOSTRIN nitric oxide synthase trafficking
NRARP NOTCH-regulated ankyrin repeat protein
NRP1 neuropilin 1
OPTC opticin
PTGS2 prostaglandin-endoperoxide synthase 2 (prostaglandin G/H synthase and cyclooxygenase)