abnormality of the anterior chamber Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Abnormality of the anterior chamber, which is the space in the eye that is behind the cornea and in front of the iris. (Human Phenotype Ontology, HP_0000593)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0000593
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24 genes associated with the abnormality of the anterior chamber phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ADAMTS10 ADAM metallopeptidase with thrombospondin type 1 motif, 10
ASXL1 additional sex combs like transcriptional regulator 1
ATOH7 atonal homolog 7 (Drosophila)
B3GALTL beta 1,3-galactosyltransferase-like
CHST14 carbohydrate (N-acetylgalactosamine 4-0) sulfotransferase 14
FBN1 fibrillin 1
FOXC1 forkhead box C1
FOXE3 forkhead box E3
ISPD isoprenoid synthase domain containing
JAG1 jagged 1
LRP5 low density lipoprotein receptor-related protein 5
LTBP2 latent transforming growth factor beta binding protein 2
MASP1 mannan-binding lectin serine peptidase 1 (C4/C2 activating component of Ra-reactive factor)
MITF microphthalmia-associated transcription factor
NDP Norrie disease (pseudoglioma)
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
RAB18 RAB18, member RAS oncogene family
SLC38A8 solute carrier family 38, member 8
TSPAN12 tetraspanin 12