uveal coloboma Gene Set

Dataset	MPO Gene-Phenotype Associations
Category	disease or phenotype associations
Type	phenotype
Description	congenital defect of the uvea in which some part of the structure is absent (Mammalian Phenotype Ontology, MP_0012533)
External Link	http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0012533
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Genes

9 gene mutations causing the uveal coloboma phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol	Name
CITED2	Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2
GLCE	glucuronic acid epimerase
HS2ST1	heparan sulfate 2-O-sulfotransferase 1
JAG1	jagged 1
MYO10	myosin X
NDST1	N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1
PAX2	paired box 2
RPS7	ribosomal protein S7
SMOC1	SPARC related modular calcium binding 1