monochromacy Gene Set

Dataset	HPO Gene-Disease Associations
Category	disease or phenotype associations
Type	phenotype
Description	Complete color blindness, a complete inability to distinguish colors. Affected persons cannot perceive colors, but only shades of gray. (Human Phenotype Ontology, HP_0007803)
External Link	http://compbio.charite.de/hpoweb/showterm?id=HP:0007803
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Genes

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

Symbol	Name
CNGA3	cyclic nucleotide gated channel alpha 3
CNGB3	cyclic nucleotide gated channel beta 3
CNNM4	cyclin and CBS domain divalent metal cation transport mediator 4
GNAT2	guanine nucleotide binding protein (G protein), alpha transducing activity polypeptide 2
OPN1LW	opsin 1 (cone pigments), long-wave-sensitive
OPN1MW	opsin 1 (cone pigments), medium-wave-sensitive