iris hypoplasia Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description Congenital underdevelopment of the iris. (Human Phenotype Ontology, HP_0007676)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0006226
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Genes

11 gene mutations causing the iris hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
BMP4 bone morphogenetic protein 4
FOXC1 forkhead box C1
FOXC2 forkhead box C2
FOXE3 forkhead box E3
LGR4 leucine-rich repeat containing G protein-coupled receptor 4
LMX1B LIM homeobox transcription factor 1, beta
MITF microphthalmia-associated transcription factor
NCAPH non-SMC condensin I complex, subunit H
PAX6 paired box 6
PXDN peroxidasin
SLC24A5 solute carrier family 24 (sodium/potassium/calcium exchanger), member 5