Dyschromatopsia Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A form of colorblindness in which only two of the three fundamental colors can be distinguished due to a lack of one of the retinal cone pigments. (Human Phenotype Ontology, HP_0007641)
External Link https://www.disgenet.org/browser/0/1/0/C0858618
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Genes

19 genes associated with the disease Dyschromatopsia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ATF6 activating transcription factor 6
CNGA3 cyclic nucleotide gated channel alpha 3
CNGB3 cyclic nucleotide gated channel beta 3
F9 coagulation factor IX
G6PD glucose-6-phosphate dehydrogenase
GNAT2 guanine nucleotide binding protein (G protein), alpha transducing activity polypeptide 2
GUCA1A guanylate cyclase activator 1A (retina)
GUCY2D guanylate cyclase 2D, membrane (retina-specific)
INS insulin
OPA1 optic atrophy 1 (autosomal dominant)
OPN1SW opsin 1 (cone pigments), short-wave-sensitive
PDE6C phosphodiesterase 6C, cGMP-specific, cone, alpha prime
PDE6H phosphodiesterase 6H, cGMP-specific, cone, gamma
POLG polymerase (DNA directed), gamma
PROM1 prominin 1
PRPH2 peripherin 2 (retinal degeneration, slow)
RPGR retinitis pigmentosa GTPase regulator
TK2 thymidine kinase 2, mitochondrial
TMEM126A transmembrane protein 126A