anterior segment dysgenesis Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Abnormal development (dysgenesis) of the anterior segment of the eye globe. These structures are mainly of mesenchymal origin. (Human Phenotype Ontology, HP_0007700)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0007700
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Genes

11 genes associated with the anterior segment dysgenesis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
B3GALTL beta 1,3-galactosyltransferase-like
FOXE3 forkhead box E3
ISPD isoprenoid synthase domain containing
JAG1 jagged 1
PIK3R1 phosphoinositide-3-kinase, regulatory subunit 1 (alpha)
PITX2 paired-like homeodomain 2
PITX3 paired-like homeodomain 3
POMT1 protein-O-mannosyltransferase 1
POMT2 protein-O-mannosyltransferase 2
PXDN peroxidasin
SLC38A8 solute carrier family 38, member 8