disorganized retinal outer plexiform layer Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description a derangement of the normal pattern of the retinal layer that is the site of synapses between the rods and cones (axons) and the horizontal and bipolar cells (dendrites) (Mammalian Phenotype Ontology, MP_0008520)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0008520
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5 gene mutations causing the disorganized retinal outer plexiform layer phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CACNA1F calcium channel, voltage-dependent, L type, alpha 1F subunit
GJA10 gap junction protein, alpha 10, 62kDa
LARGE like-glycosyltransferase
LRP5 low density lipoprotein receptor-related protein 5
RORB RAR-related orphan receptor B