abnormality of binocular vision Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormality of binocular vision, that is of the ability to synthesize the visual inputs from both eyes to a single image with perception of depth. (Human Phenotype Ontology, HP_0011514)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0011514
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10 genes associated with the abnormality of binocular vision phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ATP1A2 ATPase, Na+/K+ transporting, alpha 2 polypeptide
ATXN3 ataxin 3
CACNA1A calcium channel, voltage-dependent, P/Q type, alpha 1A subunit
MAPT microtubule-associated protein tau
PRNP prion protein
PTPN22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid)
SERPINI1 serpin peptidase inhibitor, clade I (neuroserpin), member 1
SLC2A1 solute carrier family 2 (facilitated glucose transporter), member 1
TGFB1 transforming growth factor, beta 1
TPP1 tripeptidyl peptidase I