absent retina Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description absence of the nerve layer lining the back of the eye that senses light, and creates impulses that travel through the optic nerve to the brain (Mammalian Phenotype Ontology, MP_0009773)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0009773
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1 gene mutations causing the absent retina phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
LHX2 LIM homeobox 2