| Nyctalopin ELISA Kit|
|NYX: Defects in NYX are the cause of congenital stationary night blindness type 1A (CSNB1A); also called X- linked congenital stationary night blindness (XLCSNB). Congenital stationary night blindness is a non-progressive retinal disorder characterized by impaired night vision. CSNB1A is characterized by impaired scotopic vision, myopia, hyperopia, nystagmus and reduced visual acuity. Belongs to t |
he small leucine-rich proteoglycan (SLRP) family. SLRP class IV subfamily.
Protein type: Secreted; Secreted, signal peptide
Cellular Component: cytoplasm; intracellular
Molecular Function: protein kinase inhibitor activity
Biological Process: cytokine and chemokine mediated signaling pathway; negative regulation of JAK-STAT cascade; negative regulation of protein kinase activity; visual perception
| Nyx ELISA Kit|