choroidal neovascularization Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description new, abnormal, vessel development of the thin, highly vascularized membrane covering most of the posterior of the eye between the retina and the sclera (Mammalian Phenotype Ontology, MP_0005546)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0005546
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Genes

15 gene mutations causing the choroidal neovascularization phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ADAM15 ADAM metallopeptidase domain 15
CCL13 chemokine (C-C motif) ligand 13
CCR2 chemokine (C-C motif) receptor 2
CD44 CD44 molecule (Indian blood group)
CD46 CD46 molecule, complement regulatory protein
CX3CR1 chemokine (C-X3-C motif) receptor 1
ICAM1 intercellular adhesion molecule 1
IL10 interleukin 10
ITGB2 integrin, beta 2 (complement component 3 receptor 3 and 4 subunit)
NOS1 nitric oxide synthase 1 (neuronal)
NOS2 nitric oxide synthase 2, inducible
PLAT plasminogen activator, tissue
PLAU plasminogen activator, urokinase
PLG plasminogen
VLDLR very low density lipoprotein receptor