iris atrophy Gene Set

Dataset	MPO Gene-Phenotype Associations
Category	disease or phenotype associations
Type	phenotype
Description	Atrophy of the iris. (Human Phenotype Ontology, HP_0001089)
External Link	http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0006228
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Genes

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

Symbol	Name
GPNMB	glycoprotein (transmembrane) nmb
TYRP1	tyrosinase-related protein 1