tritanomaly Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Difficulty distinguishing between yellow and blue, possible related to dysfunction of the S photopigment. (Human Phenotype Ontology, HP_0000552)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0000552
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Genes

3 genes associated with the tritanomaly phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
NR2E3 nuclear receptor subfamily 2, group E, member 3
OPA1 optic atrophy 1 (autosomal dominant)
OPN1SW opsin 1 (cone pigments), short-wave-sensitive