abnormal eye movement Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description An abnormality in voluntary or involuntary eye movements or their control. (Human Phenotype Ontology, HP_0000496)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0001389
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4 gene mutations causing the abnormal eye movement phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AP3B1 adaptor-related protein complex 3, beta 1 subunit
GRID2 glutamate receptor, ionotropic, delta 2
OPN4 opsin 4
POU4F2 POU class 4 homeobox 2