abnormal retina outer limiting membrane morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the row of junctional complexes between the plasma membranes of rod segments and the Muller glia cells; this barrier separates the layer of inner and outer segments of the rods and cones from the outer nuclear layer and forms a blood-retina barrier (Mammalian Phenotype Ontology, MP_0010236)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0010236
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3 gene mutations causing the abnormal retina outer limiting membrane morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CDKN1B cyclin-dependent kinase inhibitor 1B (p27, Kip1)
CRB1 crumbs family member 1, photoreceptor morphogenesis associated
PFDN5 prefoldin subunit 5