NYX (gene)

Nyctalopin
Identifiers
Symbols	NYX ; CLRP; CSNB1; CSNB4; MGC138447
External IDs	Template:OMIM5 Template:MGI HomoloGene: 11210
Gene ontology Molecular function Template:GNF GO Template:GNF GO Cellular component Template:GNF GO Template:GNF GO Biological process Template:GNF GO Template:GNF GO
RNA expression pattern
File:PBB GE NYX 221684 s at tn.png
More reference expression data
Orthologs
Template:GNF Ortholog box
Species	Human	Mouse
Entrez	n/a	n/a
Ensembl	n/a	n/a
UniProt	n/a	n/a
RefSeq (mRNA)	n/a	n/a
RefSeq (protein)	n/a	n/a
Location (UCSC)	n/a	n/a
PubMed search	n/a	n/a

Nyctalopin, also known as NYX, is a human gene.

Further reading

• Musarella MA, Weleber RG, Murphey WH; et al. (1990). "Assignment of the gene for complete X-linked congenital stationary night blindness (CSNB1) to Xp11.3". Genomics. 5 (4): 727–37. PMID 2574143.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Hardcastle AJ, David-Gray ZK, Jay M; et al. (1998). "Localization of CSNBX (CSNB4) between the retinitis pigmentosa loci RP2 and RP3 on proximal Xp". Invest. Ophthalmol. Vis. Sci. 38 (13): 2750–5. PMID 9418727.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Bech-Hansen NT, Naylor MJ, Maybaum TA; et al. (2000). "Mutations in NYX, encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindness". Nat. Genet. 26 (3): 319–23. doi:10.1038/81619. PMID 11062471.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Pusch CM, Zeitz C, Brandau O; et al. (2000). "The complete form of X-linked congenital stationary night blindness is caused by mutations in a gene encoding a leucine-rich repeat protein". Nat. Genet. 26 (3): 324–7. doi:10.1038/81627. PMID 11062472.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Jacobi FK, Andréasson S, Langrova H; et al. (2003). "Phenotypic expression of the complete type of X-linked congenital stationary night blindness in patients with different mutations in the NYX gene". Graefes Arch. Clin. Exp. Ophthalmol. 240 (10): 822–8. doi:10.1007/s00417-002-0562-z. PMID 12397430.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Strausberg RL, Feingold EA, Grouse LH; et al. (2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences". Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899–903. doi:10.1073/pnas.242603899. PMID 12477932.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Gregg RG, Mukhopadhyay S, Candille SI; et al. (2003). "Identification of the gene and the mutation responsible for the mouse nob phenotype". Invest. Ophthalmol. Vis. Sci. 44 (1): 378–84. PMID 12506099.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Zito I, Allen LE, Patel RJ; et al. (2003). "Mutations in the CACNA1F and NYX genes in British CSNBX families". Hum. Mutat. 21 (2): 169. doi:10.1002/humu.9106. PMID 12552565.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Zeitz C, Scherthan H, Freier S; et al. (2003). "NYX (nyctalopin on chromosome X), the gene mutated in congenital stationary night blindness, encodes a cell surface protein". Invest. Ophthalmol. Vis. Sci. 44 (10): 4184–91. PMID 14507859.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Khan NW, Kondo M, Hiriyanna KT; et al. (2005). "Primate Retinal Signaling Pathways: Suppressing ON-Pathway Activity in Monkey With Glutamate Analogues Mimics Human CSNB1-NYX Genetic Night Blindness". J. Neurophysiol. 93 (1): 481–92. doi:10.1152/jn.00365.2004. PMID 15331616.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Gerhard DS, Wagner L, Feingold EA; et al. (2004). "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)". Genome Res. 14 (10B): 2121–7. doi:10.1101/gr.2596504. PMID 15489334.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Zeitz C, Minotti R, Feil S; et al. (2005). "Novel mutations in CACNA1F and NYX in Dutch families with X-linked congenital stationary night blindness". Mol. Vis. 11: 179–83. PMID 15761389.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Ross MT, Grafham DV, Coffey AJ; et al. (2005). "The DNA sequence of the human X chromosome". Nature. 434 (7031): 325–37. doi:10.1038/nature03440. PMID 15772651.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Morgans CW, Ren G, Akileswaran L (2006). "Localization of nyctalopin in the mammalian retina". Eur. J. Neurosci. 23 (5): 1163–71. doi:10.1111/j.1460-9568.2006.04647.x. PMID 16553780.CS1 maint: Multiple names: authors list (link)
• Xiao X, Jia X, Guo X; et al. (2006). "CSNB1 in Chinese families associated with novel mutations in NYX". J. Hum. Genet. 51 (7): 634–40. doi:10.1007/s10038-006-0406-5. PMID 16670814.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Zhang Q, Xiao X, Li S; et al. (2007). "Mutations in NYX of individuals with high myopia, but without night blindness". Mol. Vis. 13: 330–6. PMID 17392683.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)