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Protein Page:
NYX (human)

Overview
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 the small leucine-rich proteoglycan (SLRP) family. SLRP class IV subfamily. Note: This description may include information from UniProtKB.
Protein type: Secreted; Secreted, signal peptide
Chromosomal Location of Human Ortholog: Xp11.4
Cellular Component: proteinaceous extracellular matrix; intracellular
Biological Process: visual perception; response to stimulus
Reference #:  Q9GZU5 (UniProtKB)
Alt. Names/Synonyms: CLRP; CSNB1; CSNB4; leucine-rich repeat protein; MGC138447; Nyctalopin; NYX
Gene Symbols: NYX
Molecular weight: 52,000 Da
Basal Isoelectric point: 9.1  Predict pI for various phosphorylation states
Select Structure to View Below

NYX

Protein Structure Not Found.


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Modification Sites and Domains  

Modification Sites in Parent Protein, Orthologs, and Isoforms  
 

Show Multiple Sequence Alignment


 SS 

SS: The number of records in which this modification site was determined using site-specific methods. SS methods include amino acid sequencing, site-directed mutagenesis, modification site-specific antibodies, specific MS strategies, etc.


 MS 

MS: The number of records in which this modification site was assigned using ONLY proteomic discovery-mode mass spectrometry.


       human

 
0 1 Y284-p LAELELLyLDRNSIA
0 1 S364-p VTDVPCAsPGsVAGL
0 1 S367-p VPCAsPGsVAGLDLS
0 2 T377-p GLDLSQVtFGRSSDG
  mouse

 
Y279 LAELELLYLDRNSIT
S359 VADVACASPGSVAGQ
S362 VACASPGSVAGQDLS
V372 GQDLSQVVFERSSDG
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