red-green dyschromatopsia Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Difficulty with discriminating red and green hues. (Human Phenotype Ontology, HP_0000642)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0000642
Similar Terms
Downloads & Tools

Genes

4 genes associated with the red-green dyschromatopsia 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)
OPN1LW opsin 1 (cone pigments), long-wave-sensitive
OPN1MW opsin 1 (cone pigments), medium-wave-sensitive