absent retinal ganglion layer Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description absence of the innermost nuclear layer of the retina, which contains neurons that project axons through the optic nerve to the brain (Mammalian Phenotype Ontology, MP_0008510)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0008510
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Genes

2 gene mutations causing the absent retinal ganglion layer phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ATOH7 atonal homolog 7 (Drosophila)
TFAP2A transcription factor AP-2 alpha (activating enhancer binding protein 2 alpha)