corneal vascularization Gene Set
Genes
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
|