Hemeralopia Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A visual defect characterized by the inability to see as clearly in bright light as in dim light. The word hemeralopia literally means day blindness. (Human Phenotype Ontology, HP_0012047)
External Link https://www.disgenet.org/browser/0/1/0/C0018975
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Genes

12 genes associated with the disease Hemeralopia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ATXN7 ataxin 7
CLN6 ceroid-lipofuscinosis, neuronal 6, late infantile, variant
CNGA3 cyclic nucleotide gated channel alpha 3
GRM6 glutamate receptor, metabotropic 6
GUCY2D guanylate cyclase 2D, membrane (retina-specific)
NR2E3 nuclear receptor subfamily 2, group E, member 3
NYX nyctalopin
SAG S-antigen; retina and pineal gland (arrestin)
TSEN2 TSEN2 tRNA splicing endonuclease subunit
TSEN34 TSEN34 tRNA splicing endonuclease subunit
TSEN54 TSEN54 tRNA splicing endonuclease subunit
TTPA tocopherol (alpha) transfer protein