Progressive Cone Dystrophy (Without Rod Involvement) Gene Set

Dataset	DisGeNET Gene-Disease Associations
Category	disease or phenotype associations
Type	disease
External Link	https://www.disgenet.org/browser/0/1/0/C0271092
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Genes

9 genes associated with the disease Progressive Cone Dystrophy (Without Rod Involvement) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol	Name
ABCA4	ATP-binding cassette, sub-family A (ABC1), member 4
CACNA1F	calcium channel, voltage-dependent, L type, alpha 1F subunit
CNGB3	cyclic nucleotide gated channel beta 3
GNAT2	guanine nucleotide binding protein (G protein), alpha transducing activity polypeptide 2
GUCA1A	guanylate cyclase activator 1A (retina)
KCNV2	potassium channel, voltage gated modifier subfamily V, member 2
MKKS	McKusick-Kaufman syndrome
PDE6C	phosphodiesterase 6C, cGMP-specific, cone, alpha prime
PRPH2	peripherin 2 (retinal degeneration, slow)