congenital glaucoma Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
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19 genes associated with the congenital glaucoma phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
AKT1 v-akt murine thymoma viral oncogene homolog 1
ATOH7 atonal homolog 7 (Drosophila)
B3GAT3 beta-1,3-glucuronyltransferase 3
CANT1 calcium activated nucleotidase 1
CYP1B1 cytochrome P450, family 1, subfamily B, polypeptide 1
FGFR2 fibroblast growth factor receptor 2
GLIS3 GLIS family zinc finger 3
GNAQ guanine nucleotide binding protein (G protein), q polypeptide
LTBP2 latent transforming growth factor beta binding protein 2
OCRL oculocerebrorenal syndrome of Lowe
PAX6 paired box 6
PITX2 paired-like homeodomain 2
POMGNT1 protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-)
POMT1 protein-O-mannosyltransferase 1
POMT2 protein-O-mannosyltransferase 2
PTEN phosphatase and tensin homolog
PXDN peroxidasin
PYCR1 pyrroline-5-carboxylate reductase 1
TWIST1 twist family bHLH transcription factor 1