abnormal corneal epithelium morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the smooth stratified squamous epithelium that covers the outer surface of the cornea (Mammalian Phenotype Ontology, MP_0006000)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0006000
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34 gene mutations causing the abnormal corneal epithelium morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ADAM17 ADAM metallopeptidase domain 17
ARNTL aryl hydrocarbon receptor nuclear translocator-like
ARSB arylsulfatase B
BNC1 basonuclin 1
CENPJ centromere protein J
CHUK conserved helix-loop-helix ubiquitous kinase
COL8A2 collagen, type VIII, alpha 2
CTNNB1 catenin (cadherin-associated protein), beta 1, 88kDa
DKK2 dickkopf WNT signaling pathway inhibitor 2
DSTN destrin (actin depolymerizing factor)
EDA ectodysplasin A
FOXC1 forkhead box C1
FOXE3 forkhead box E3
FREM1 FRAS1 related extracellular matrix 1
GRIP1 glutamate receptor interacting protein 1
INHBB inhibin, beta B
KLHL20 kelch-like family member 20
KRT12 keratin 12, type I
KRT14 keratin 14, type I
KRT4 keratin 4, type II
LGR4 leucine-rich repeat containing G protein-coupled receptor 4
LIMK2 LIM domain kinase 2
MSX2 msh homeobox 2
NRTN neurturin
PAX6 paired box 6
PITX2 paired-like homeodomain 2
PLG plasminogen
PLTP phospholipid transfer protein
PXDN peroxidasin
SLC4A11 solute carrier family 4, sodium borate transporter, member 11
TCF7L1 transcription factor 7-like 1 (T-cell specific, HMG-box)
THBS1 thrombospondin 1
TP63 tumor protein p63
ZEB1 zinc finger E-box binding homeobox 1