abnormal iridocorneal angle Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the acute angle occurring between the iris and the cornea at the periphery of the anterior chamber of the eye (Mammalian Phenotype Ontology, MP_0004221)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004221
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19 gene mutations causing the abnormal iridocorneal angle phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ADAM17 ADAM metallopeptidase domain 17
BMP4 bone morphogenetic protein 4
CENPJ centromere protein J
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
KERA keratocan
LGR4 leucine-rich repeat containing G protein-coupled receptor 4
LMX1B LIM homeobox transcription factor 1, beta
LYST lysosomal trafficking regulator
PAX6 paired box 6
PRSS56 protease, serine, 56
PXDN peroxidasin
SPNS2 spinster homolog 2 (Drosophila)
TCF7L1 transcription factor 7-like 1 (T-cell specific, HMG-box)
VAV2 vav 2 guanine nucleotide exchange factor
ZEB1 zinc finger E-box binding homeobox 1