Complete Congenital Stationary Night Blindness Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C4048798
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Genes

6 genes associated with the disease Complete Congenital Stationary Night Blindness 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
GPR179 G protein-coupled receptor 179
GRM6 glutamate receptor, metabotropic 6
LRIT3 leucine-rich repeat, immunoglobulin-like and transmembrane domains 3
NYX nyctalopin
TRPM1 transient receptor potential cation channel, subfamily M, member 1