congenital stationary night blindness Gene Set

Dataset	DISEASES Curated Gene-Disease Association Evidence Scores
Category	disease or phenotype associations
Type	disease
Description	A night blindness that is characterized by hemeralopia with a moderate loss of visual acuity and caused by defective photoreceptor-to-bipolar cell signaling with common ERG findings of reduced or absent b-waves and generally normal a-waves. (Human Disease Ontology, DOID_0050534)
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Genes

13 genes involed in the disease congenital stationary night blindness from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

Symbol	Name
CABP4	calcium binding protein 4
CACNA1F	calcium channel, voltage-dependent, L type, alpha 1F subunit
GNAT1	guanine nucleotide binding protein (G protein), alpha transducing activity polypeptide 1
GPR179	G protein-coupled receptor 179
GRK1	G protein-coupled receptor kinase 1
GRM6	glutamate receptor, metabotropic 6
LRIT3	leucine-rich repeat, immunoglobulin-like and transmembrane domains 3
NYX	nyctalopin
PDE6B	phosphodiesterase 6B, cGMP-specific, rod, beta
RHO	rhodopsin
SAG	S-antigen; retina and pineal gland (arrestin)
SLC24A1	solute carrier family 24 (sodium/potassium/calcium exchanger), member 1
TRPM1	transient receptor potential cation channel, subfamily M, member 1