abnormal retinal melanin granule morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the pigment particles in the retina (Mammalian Phenotype Ontology, MP_0010192)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0010192
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Genes

2 gene mutations causing the abnormal retinal melanin granule morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
KXD1 KxDL motif containing 1
PMEL premelanosome protein