absent visual evoked potential Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description absence of a characteristic electroencephalographic pattern recorded from the occipital area generated in response to retinal stimulation such as flashing lights or inverting a contrasting image; absence may indicate blindness (Mammalian Phenotype Ontology, MP_0010749)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0010749
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2 gene mutations causing the absent visual evoked potential phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CACNA1F calcium channel, voltage-dependent, L type, alpha 1F subunit
NYX nyctalopin