Enhanced S-Cone Syndrome Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C1849394
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Genes

14 genes associated with the disease Enhanced S-Cone Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
CACNA1F calcium channel, voltage-dependent, L type, alpha 1F subunit
CNGA3 cyclic nucleotide gated channel alpha 3
CRB1 crumbs family member 1, photoreceptor morphogenesis associated
FRMD4B FERM domain containing 4B
GRK1 G protein-coupled receptor kinase 1
GRK7 G protein-coupled receptor kinase 7
GUCA1A guanylate cyclase activator 1A (retina)
NR2E3 nuclear receptor subfamily 2, group E, member 3
NRL neural retina leucine zipper
NYX nyctalopin
OPN1LW opsin 1 (cone pigments), long-wave-sensitive
PRPF8 pre-mRNA processing factor 8
RPE65 retinal pigment epithelium-specific protein 65kDa
TAAR5 trace amine associated receptor 5