abnormal visual evoked potential Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description An anomaly of visually evoked potentials (VEP), which are electrical potentials, initiated by brief visual stimuli, which are recorded from the scalp overlying the visual cortex. (Human Phenotype Ontology, HP_0000649)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0010748
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Genes

9 gene mutations causing the abnormal 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
CDKL5 cyclin-dependent kinase-like 5
CLDN11 claudin 11
CNTNAP1 contactin associated protein 1
CSF1 colony stimulating factor 1 (macrophage)
HAPLN2 hyaluronan and proteoglycan link protein 2
NYX nyctalopin
OPA1 optic atrophy 1 (autosomal dominant)
TENM2 teneurin transmembrane protein 2