abnormal corneal endothelium morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the single layer of large flattened cells that cover the surface of the cornea (Mammalian Phenotype Ontology, MP_0005301)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0005301
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12 gene mutations causing the abnormal corneal endothelium morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ADAM17 ADAM metallopeptidase domain 17
CENPJ centromere protein J
COL8A2 collagen, type VIII, alpha 2
FOXC1 forkhead box C1
FOXE3 forkhead box E3
MAN2B1 mannosidase, alpha, class 2B, member 1
PAX6 paired box 6
PEX3 peroxisomal biogenesis factor 3
PITX2 paired-like homeodomain 2
SLC4A11 solute carrier family 4, sodium borate transporter, member 11
TGFB2 transforming growth factor, beta 2
ZEB1 zinc finger E-box binding homeobox 1