abnormal visual acuity Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any abnormality in the spatial resolution or resolving power of the visual processing system (Mammalian Phenotype Ontology, MP_0011832)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0011832
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4 gene mutations causing the abnormal visual acuity phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CFH complement factor H
CHRNB2 cholinergic receptor, nicotinic, beta 2 (neuronal)
OTX2 orthodenticle homeobox 2
PDE6B phosphodiesterase 6B, cGMP-specific, rod, beta