abnormal retinal melanocyte morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the cells that produce pigment in the retina (Mammalian Phenotype Ontology, MP_0010190)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0010190
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2 gene mutations causing the abnormal retinal melanocyte morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
KXD1 KxDL motif containing 1
PMEL premelanosome protein