abnormal ciliary body pigmentation Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description anomalous coloring of the thickened portion of the vascular tunic, which lies between the choroid and the iris (Mammalian Phenotype Ontology, MP_0005101)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0005101
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4 gene mutations causing the abnormal ciliary body pigmentation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
GPR143 G protein-coupled receptor 143
HPS1 Hermansky-Pudlak syndrome 1
LYST lysosomal trafficking regulator
SLC24A5 solute carrier family 24 (sodium/potassium/calcium exchanger), member 5