abnormal canal of schlemm morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly in the vascular structure encircling the anterior chamber of the eye, through which the aqueous humor is returned to the blood circulation (Mammalian Phenotype Ontology, MP_0005204)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0005204
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8 gene mutations causing the abnormal canal of schlemm morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ADAM17 ADAM metallopeptidase domain 17
BMP4 bone morphogenetic protein 4
CYP1B1 cytochrome P450, family 1, subfamily B, polypeptide 1
FOXC1 forkhead box C1
FOXC2 forkhead box C2
FOXE3 forkhead box E3
FOXF2 forkhead box F2
LGR4 leucine-rich repeat containing G protein-coupled receptor 4