Color Vision Defects Gene Set

Dataset HuGE Navigator Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
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Genes

9 genes associated with the Color Vision Defects phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Symbol Name
ABCA4 ATP-binding cassette, sub-family A (ABC1), member 4
BDNF brain-derived neurotrophic factor
CNGA3 cyclic nucleotide gated channel alpha 3
CNGB3 cyclic nucleotide gated channel beta 3
GNAT2 guanine nucleotide binding protein (G protein), alpha transducing activity polypeptide 2
KCNV2 potassium channel, voltage gated modifier subfamily V, member 2
LRRK2 leucine-rich repeat kinase 2
PDE6C phosphodiesterase 6C, cGMP-specific, cone, alpha prime
RPGR retinitis pigmentosa GTPase regulator