corneal vascularization Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description formation of blood vessels in the cornea, which normally lacks vessels (Mammalian Phenotype Ontology, MP_0005542)
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33 gene mutations causing the corneal vascularization phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ARNTL aryl hydrocarbon receptor nuclear translocator-like
CCR5 chemokine (C-C motif) receptor 5 (gene/pseudogene)
CISD2 CDGSH iron sulfur domain 2
COL4A1 collagen, type IV, alpha 1
CSRP2BP CSRP2 binding protein
CXCR2 chemokine (C-X-C motif) receptor 2
DSTN destrin (actin depolymerizing factor)
EDA ectodysplasin A
FIGN fidgetin
FLT1 fms-related tyrosine kinase 1
FOXC1 forkhead box C1
FOXE3 forkhead box E3
FOXN1 forkhead box N1
IFNAR1 interferon (alpha, beta and omega) receptor 1
IFNG interferon, gamma
LGR4 leucine-rich repeat containing G protein-coupled receptor 4
LMX1B LIM homeobox transcription factor 1, beta
MCPH1 microcephalin 1
MYH9 myosin, heavy chain 9, non-muscle
NOTCH1 notch 1
PAX6 paired box 6
PEX3 peroxisomal biogenesis factor 3
PGF placental growth factor
PLG plasminogen
PPP1R13L protein phosphatase 1, regulatory subunit 13 like
PRDX6 peroxiredoxin 6
SFRP2 secreted frizzled-related protein 2
SPNS2 spinster homolog 2 (Drosophila)
TMC8 transmembrane channel-like 8
TRPC3 transient receptor potential cation channel, subfamily C, member 3
TRPC4AP transient receptor potential cation channel, subfamily C, member 4 associated protein
UCP1 uncoupling protein 1 (mitochondrial, proton carrier)
VEGFB vascular endothelial growth factor B