rod monochromacy Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A condition where the retina contains no functional cone cells, so that in addition to the absence of color discrimination, vision in lights of normal intensity is difficult. (Human Phenotype Ontology, HP_0011516)
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2 genes associated with the rod 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
GNAT2 guanine nucleotide binding protein (G protein), alpha transducing activity polypeptide 2