Autosomal Dominant Congenital Stationary Night Blindness

Autosomal Dominant Congenital Stationary Night Blindness, also known as night blindness, congenital stationary, autosomal dominant, is related to congenital stationary night blindness and night blindness. An important gene associated with Autosomal Dominant Congenital Stationary Night Blindness is GNAT1 (G Protein Subunit Alpha Transducin 1), and among its related pathways/superpathways are Visual phototransduction and Visual Cycle in Retinal Rods. Affiliated tissues include retina and eye, and related phenotypes are Increased shRNA abundance (Z-score > 2) and pigmentation