absent optic disc Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description absence of the area in the retina where all of the axons of the ganglion cells exit the retina to form the optic nerve (Mammalian Phenotype Ontology, MP_0011389)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0011389
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2 gene mutations causing the absent optic disc phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
MTERF4 mitochondrial transcription termination factor 4
TFB1M transcription factor B1, mitochondrial