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NYX cDNA ORF clone, Homo sapiens (human)

Gene Symbol NYX
Entrez Gene ID 60506
Full Name nyctalopin
Synonyms CLRP, CSNB1, CSNB1A, CSNB4, NBM1
Gene Type protein-coding
Organism Homo sapiens (human)
Genome

X

Xp11.4

Summary The product of this gene belongs to the small leucine-rich proteoglycan (SLRP) family of proteins. Defects in this gene are the cause of congenital stationary night blindness type 1 (CSNB1), also called X-linked congenital stationary night blindness (XLCSNB). CSNB1 is a rare inherited retinal disorder characterized by impaired scotopic vision, myopia, hyperopia, nystagmus and reduced visual acuity. The role of other SLRP proteins suggests that mutations in this gene disrupt developing retinal interconnections involving the ON-bipolar cells, leading to the visual losses seen in patients with complete CSNB. [provided by RefSeq, Oct 2008]. lac of sum
Disorder MIM:

300278

Disorder Html: Night blindness, congenital stationary, type 1, 310500 (3)

mRNA and Protein(s)

mRNA Protein Name
NM_022567 NP_072089 nyctalopin precursor
XM_005272632 XP_005272689 nyctalopin isoform X1


Homo sapiens (human) NYX NP_072089.1
Pan troglodytes (chimpanzee) NYX XP_001138632.2
Macaca mulatta (Rhesus monkey) SLRN XP_001087613.1
Canis lupus familiaris (dog) NYX XP_005641316.1
Bos taurus (cattle) NYX XP_005228361.1
Mus musculus (house mouse) Nyx NP_775591.1
Rattus norvegicus (Norway rat) Nyx NP_001094437.1
Gallus gallus (chicken) NYX XP_004934667.1
Danio rerio (zebrafish) nyx NP_001071085.1
Xenopus (Silurana) tropicalis (western clawed frog) nyx XP_002932845.2


GeneRIFs: Gene References Into Functions What's a GeneRIF?

The following NYX gene cDNA ORF clone sequences were retrieved from the NCBI Reference Sequence Database (RefSeq). These sequences represent the protein coding region of the NYX cDNA ORF which is encoded by the open reading frame (ORF) sequence. ORF sequences can be delivered in our standard vector, pcDNA3.1+/C-(K)DYK or the vector of your choice as an expression/transfection-ready ORF clone. Not the clone you want? Click here to find your clone.

***CloneID RefSeq Accession Definition **Vector *Turnaround time Price Select
OHu19068
NM_022567 Homo sapiens nyctalopin (NYX), mRNA. pcDNA3.1+/C-(K)DYK or customized vector
in pcDNA3.1+/C-(K)DYK
$159.50-$223.30
$319.00
OHu19068
XM_005272632 PREDICTED: Homo sapiens nyctalopin (NYX), transcript variant X1, mRNA. pcDNA3.1+/C-(K)DYK or customized vector
in pcDNA3.1+/C-(K)DYK
$159.50-$223.30
$319.00
Next-day Shipping ORF Clones ( in default vector with tag)
1 Clone 30% OFF
2-4 Clone 40% OFF
5 or more Clone 50% OFF
All Other ORF Clones
30% OFF

*Business Day

** You may select a custom vector to replace pcDNA3.1+/C-(K)DYK after clone is added to cart.

** GenScript guarantees 100% sequence accuracy of all synthetic DNA constructs we deliver, but we do not guarantee protein expression in your experimental system. Protein expression is influenced by many factors that may vary between experiments or laboratories. In addition, please pay attention to the signal peptide, propeptide and transit peptide in target ORF, which may affect the choice of vector (N/C terminal tag vector).

***One clone ID might be correlated to multiple accession numbers, which share the same CDS sequence.


CloneID OHu19068
Clone ID Related Accession (Same CDS sequence) NM_022567 , XM_005272632
Accession Version NM_022567.2 Documents for ORF clone product in dufault vector
Sequence Information ORF Nucleotide Sequence (Length: 1446bp)
Protein sequence
SNP
Vector pcDNA3.1+/C-(K)DYK or customized vector User Manual
Clone information Clone Map MSDS
Tag on pcDNA3.1+/C-(K)DYK C terminal DYKDDDDK tags COA
ORF Insert Method CloneEZ® Seamless cloning technology
Structure linear
Update Date 03-MAY-2014
Organism Homo sapiens (human)
Product nyctalopin precursor
Comment REVIEWED REFSEQ: This record has been curated by NCBI staff. The reference sequence was derived from AJ278865.1. This sequence is a reference standard in the RefSeqGene project. On Sep 13, 2008 this sequence version replaced gi:12007645. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Gene record to access additional publications. ##Evidence-Data-START## Transcript exon combination :: AJ278865.1, BC112242.1 [ECO:0000332] ##Evidence-Data-END## COMPLETENESS: complete on the 3' end.

1
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181
241
301
361
421
481
541
601
661
721
781
841
901
961
1021
1081
1141
1201
1261
1321
1381
1441
ATGAAAGGCC GAGGGATGTT GGTCCTGCTT CTGCATGCGG TGGTCCTCGG CCTGCCCAGC 
GCCTGGGCCG TGGGGGCCTG CGCCCGCGCT TGTCCCGCCG CCTGCGCCTG CAGCACCGTG
GAGCGCGGCT GCTCGGTGCG CTGCGACCGC GCGGGCCTCC TGCGGGTGCC GGCCGAGCTC
CCGTGCGAGG CGGTCTCCAT CGACCTGGAC CGGAACGGCC TGCGCTTCCT GGGCGAGCGA
GCCTTCGGCA CGCTGCCGTC CTTGCGCCGC CTGTCGCTGC GCCACAACAA CCTGTCCTTC
ATCACGCCCG GCGCCTTCAA GGGCCTGCCG CGCCTGGCTG AGCTGCGCCT GGCGCACAAC
GGCGACCTGC GCTACCTGCA CGCGCGCACC TTCGCGGCGC TCAGCCGCCT GCGCCGCCTA
GACCTAGCAG CCTGCCGCCT CTTCAGCGTG CCCGAGCGCC TCCTGGCCGA ACTGCCGGCC
CTGCGCGAAC TCGCCGCCTT CGACAACCTG TTCCGCCGCG TGCCGGGCGC GCTGCGCGGC
CTGGCCAACC TGACGCACGC GCACCTGGAG CGCGGCCGCA TCGAGGCGGT GGCCTCCAGC
TCGCTGCAGG GCCTGCGCCG CCTGCGCTCG CTCAGCCTGC AGGCCAACCG CGTCCGTGCC
GTGCACGCTG GCGCCTTCGG GGACTGTGGC GTCCTGGAGC ATCTGCTGCT CAACGACAAC
CTGCTGGCCG AGCTCCCGGC CGACGCCTTC CGCGGCCTGC GGCGCCTGCG CACGCTCAAC
CTGGGTGGCA ACGCGCTGGA CCGCGTGGCG CGCGCCTGGT TCGCTGACCT GGCCGAGCTC
GAGCTGCTCT ACCTGGACCG CAACAGCATC GCCTTCGTGG AGGAGGGCGC CTTCCAGAAC
CTCTCGGGTC TCCTCGCGCT GCACCTCAAC GGCAACCGCC TCACCGTGCT CGCCTGGGTC
GCCTTCCAGC CCGGCTTCTT CCTGGGCCGC CTCTTCCTCT TCCGCAACCC GTGGTGCTGC
GACTGCCGTC TGGAGTGGCT GAGGGACTGG ATGGAGGGCT CCGGACGTGT CACCGACGTG
CCGTGCGCCT CCCCGGGCTC CGTGGCCGGC CTGGACCTCA GCCAGGTGAC CTTCGGGCGC
TCCTCCGATG GCCTCTGTGT GGACCCCGAG GAGCTGAACC TCACCACGTC CAGTCCAGGC
CCGTCCCCAG AACCAGCGGC CACCACCGTG AGCAGGTTCA GCAGCCTCCT CTCCAAGCTG
CTGGCCCCGA GGGTCCCGGT GGAGGAGGCG GCCAACACCA CTGGGGGGCT GGCCAACGCC
TCCCTGTCCG ACAGCCTCTC CTCCCGTGGG GTGGGAGGCG CGGGCCGGCA GCCCTGGTTT
CTCCTCGCCT CTTGTCTCCT GCCCAGCGTG GCCCAGCACG TGGTGTTTGG CCTGCAGATG
GACTGA

The stop codons will be deleted if pcDNA3.1+/C-(K)DYK vector is selected.

RefSeq NP_072089.1
CDS431..1876
Misc Feature(1)416..418(+)
Misc Feature(2)617..682(+)
Misc Feature(3)632..691(+)
Misc Feature(4)647..1381(+)
Misc Feature(5)686..871(+)
Misc Feature(6)689..754(+)
Misc Feature(7)692..1381(+)
Misc Feature(8)692..763(+)
Misc Feature(9)713..1288(+)
Misc Feature(10)761..820(+)
Misc Feature(11)764..838(+)
Misc Feature(12)836..907(+)
Misc Feature(13)839..910(+)
Misc Feature(14)908..976(+)
Misc Feature(15)911..979(+)
Misc Feature(16)977..1156(+)
Misc Feature(17)977..1042(+)
Misc Feature(18)980..1051(+)
Misc Feature(19)1049..1114(+)
Misc Feature(20)1052..1123(+)
Misc Feature(21)1121..1186(+)
Misc Feature(22)1124..1300(+)
Misc Feature(23)1124..1195(+)
Misc Feature(24)1193..1258(+)
Misc Feature(25)1196..1267(+)
Misc Feature(26)1265..1330(+)
Misc Feature(27)1268..>1399(+)
Misc Feature(28)1268..1333(+)
Misc Feature(29)1337..1402(+)
Misc Feature(30)1436..>1540(+)
Exon (1)1..467
Gene:NYX
Gene Synonym:
Exon (2)468..2629
Gene:NYX
Gene Synonym:
Translation

Target ORF information:

RefSeq Version NM_022567
Organism Homo sapiens (human)
Definition Homo sapiens nyctalopin (NYX), mRNA.

Target ORF information:

Epitope DYKDDDDK
Bacterial selection AMPR
Mammalian selection NeoR
Vector pcDNA3.1+/C-(K)DYK
NM_022567

ORF Insert Sequence:

1
61
121
181
241
301
361
421
481
541
601
661
721
781
841
901
961
1021
1081
1141
1201
1261
1321
1381
1441
ATGAAAGGCC GAGGGATGTT GGTCCTGCTT CTGCATGCGG TGGTCCTCGG CCTGCCCAGC 
GCCTGGGCCG TGGGGGCCTG CGCCCGCGCT TGTCCCGCCG CCTGCGCCTG CAGCACCGTG
GAGCGCGGCT GCTCGGTGCG CTGCGACCGC GCGGGCCTCC TGCGGGTGCC GGCCGAGCTC
CCGTGCGAGG CGGTCTCCAT CGACCTGGAC CGGAACGGCC TGCGCTTCCT GGGCGAGCGA
GCCTTCGGCA CGCTGCCGTC CTTGCGCCGC CTGTCGCTGC GCCACAACAA CCTGTCCTTC
ATCACGCCCG GCGCCTTCAA GGGCCTGCCG CGCCTGGCTG AGCTGCGCCT GGCGCACAAC
GGCGACCTGC GCTACCTGCA CGCGCGCACC TTCGCGGCGC TCAGCCGCCT GCGCCGCCTA
GACCTAGCAG CCTGCCGCCT CTTCAGCGTG CCCGAGCGCC TCCTGGCCGA ACTGCCGGCC
CTGCGCGAAC TCGCCGCCTT CGACAACCTG TTCCGCCGCG TGCCGGGCGC GCTGCGCGGC
CTGGCCAACC TGACGCACGC GCACCTGGAG CGCGGCCGCA TCGAGGCGGT GGCCTCCAGC
TCGCTGCAGG GCCTGCGCCG CCTGCGCTCG CTCAGCCTGC AGGCCAACCG CGTCCGTGCC
GTGCACGCTG GCGCCTTCGG GGACTGTGGC GTCCTGGAGC ATCTGCTGCT CAACGACAAC
CTGCTGGCCG AGCTCCCGGC CGACGCCTTC CGCGGCCTGC GGCGCCTGCG CACGCTCAAC
CTGGGTGGCA ACGCGCTGGA CCGCGTGGCG CGCGCCTGGT TCGCTGACCT GGCCGAGCTC
GAGCTGCTCT ACCTGGACCG CAACAGCATC GCCTTCGTGG AGGAGGGCGC CTTCCAGAAC
CTCTCGGGTC TCCTCGCGCT GCACCTCAAC GGCAACCGCC TCACCGTGCT CGCCTGGGTC
GCCTTCCAGC CCGGCTTCTT CCTGGGCCGC CTCTTCCTCT TCCGCAACCC GTGGTGCTGC
GACTGCCGTC TGGAGTGGCT GAGGGACTGG ATGGAGGGCT CCGGACGTGT CACCGACGTG
CCGTGCGCCT CCCCGGGCTC CGTGGCCGGC CTGGACCTCA GCCAGGTGAC CTTCGGGCGC
TCCTCCGATG GCCTCTGTGT GGACCCCGAG GAGCTGAACC TCACCACGTC CAGTCCAGGC
CCGTCCCCAG AACCAGCGGC CACCACCGTG AGCAGGTTCA GCAGCCTCCT CTCCAAGCTG
CTGGCCCCGA GGGTCCCGGT GGAGGAGGCG GCCAACACCA CTGGGGGGCT GGCCAACGCC
TCCCTGTCCG ACAGCCTCTC CTCCCGTGGG GTGGGAGGCG CGGGCCGGCA GCCCTGGTTT
CTCCTCGCCT CTTGTCTCCT GCCCAGCGTG GCCCAGCACG TGGTGTTTGG CCTGCAGATG
GACTGA

The stop codons will be deleted if pcDNA3.1+/C-(K)DYK vector is selected.

CloneID OHu19068
Clone ID Related Accession (Same CDS sequence) NM_022567 , XM_005272632
Accession Version XM_005272632.2 Documents for ORF clone product in dufault vector
Sequence Information ORF Nucleotide Sequence (Length: 1446bp)
Protein sequence
SNP
Vector pcDNA3.1+/C-(K)DYK or customized vector User Manual
Clone information Clone Map MSDS
Tag on pcDNA3.1+/C-(K)DYK C terminal DYKDDDDK tags COA
ORF Insert Method CloneEZ® Seamless cloning technology
Structure linear
Update Date 12-MAR-2015
Organism Homo sapiens (human)
Product nyctalopin isoform X1
Comment MODEL REFSEQ: This record is predicted by automated computational analysis. This record is derived from a genomic sequence (NT_079573.5) annotated using gene prediction method: Gnomon, supported by mRNA evidence. Also see: Documentation of NCBI's Annotation Process On Mar 12, 2015 this sequence version replaced gi:530421506. ##Genome-Annotation-Data-START## Annotation Provider :: NCBI Annotation Status :: Full annotation Annotation Version :: Homo sapiens Annotation Release 107 Annotation Pipeline :: NCBI eukaryotic genome annotation pipeline Annotation Software Version :: 6.2 Annotation Method :: Best-placed RefSeq; Gnomon Features Annotated :: Gene; mRNA; CDS; ncRNA ##Genome-Annotation-Data-END##

1
61
121
181
241
301
361
421
481
541
601
661
721
781
841
901
961
1021
1081
1141
1201
1261
1321
1381
1441
ATGAAAGGCC GAGGGATGTT GGTCCTGCTT CTGCATGCGG TGGTCCTCGG CCTGCCCAGC 
GCCTGGGCCG TGGGGGCCTG CGCCCGCGCT TGTCCCGCCG CCTGCGCCTG CAGCACCGTG
GAGCGCGGCT GCTCGGTGCG CTGCGACCGC GCGGGCCTCC TGCGGGTGCC GGCCGAGCTC
CCGTGCGAGG CGGTCTCCAT CGACCTGGAC CGGAACGGCC TGCGCTTCCT GGGCGAGCGA
GCCTTCGGCA CGCTGCCGTC CTTGCGCCGC CTGTCGCTGC GCCACAACAA CCTGTCCTTC
ATCACGCCCG GCGCCTTCAA GGGCCTGCCG CGCCTGGCTG AGCTGCGCCT GGCGCACAAC
GGCGACCTGC GCTACCTGCA CGCGCGCACC TTCGCGGCGC TCAGCCGCCT GCGCCGCCTA
GACCTAGCAG CCTGCCGCCT CTTCAGCGTG CCCGAGCGCC TCCTGGCCGA ACTGCCGGCC
CTGCGCGAAC TCGCCGCCTT CGACAACCTG TTCCGCCGCG TGCCGGGCGC GCTGCGCGGC
CTGGCCAACC TGACGCACGC GCACCTGGAG CGCGGCCGCA TCGAGGCGGT GGCCTCCAGC
TCGCTGCAGG GCCTGCGCCG CCTGCGCTCG CTCAGCCTGC AGGCCAACCG CGTCCGTGCC
GTGCACGCTG GCGCCTTCGG GGACTGTGGC GTCCTGGAGC ATCTGCTGCT CAACGACAAC
CTGCTGGCCG AGCTCCCGGC CGACGCCTTC CGCGGCCTGC GGCGCCTGCG CACGCTCAAC
CTGGGTGGCA ACGCGCTGGA CCGCGTGGCG CGCGCCTGGT TCGCTGACCT GGCCGAGCTC
GAGCTGCTCT ACCTGGACCG CAACAGCATC GCCTTCGTGG AGGAGGGCGC CTTCCAGAAC
CTCTCGGGTC TCCTCGCGCT GCACCTCAAC GGCAACCGCC TCACCGTGCT CGCCTGGGTC
GCCTTCCAGC CCGGCTTCTT CCTGGGCCGC CTCTTCCTCT TCCGCAACCC GTGGTGCTGC
GACTGCCGTC TGGAGTGGCT GAGGGACTGG ATGGAGGGCT CCGGACGTGT CACCGACGTG
CCGTGCGCCT CCCCGGGCTC CGTGGCCGGC CTGGACCTCA GCCAGGTGAC CTTCGGGCGC
TCCTCCGATG GCCTCTGTGT GGACCCCGAG GAGCTGAACC TCACCACGTC CAGTCCAGGC
CCGTCCCCAG AACCAGCGGC CACCACCGTG AGCAGGTTCA GCAGCCTCCT CTCCAAGCTG
CTGGCCCCGA GGGTCCCGGT GGAGGAGGCG GCCAACACCA CTGGGGGGCT GGCCAACGCC
TCCCTGTCCG ACAGCCTCTC CTCCCGTGGG GTGGGAGGCG CGGGCCGGCA GCCCTGGTTT
CTCCTCGCCT CTTGTCTCCT GCCCAGCGTG GCCCAGCACG TGGTGTTTGG CCTGCAGATG
GACTGA

The stop codons will be deleted if pcDNA3.1+/C-(K)DYK vector is selected.

RefSeq XP_005272689.1
CDS169..1614
Misc Feature(1)370..429(+)
Misc Feature(2)385..1119(+)
Misc Feature(3)424..609(+)
Misc Feature(4)430..1119(+)
Misc Feature(5)430..501(+)
Misc Feature(6)451..1026(+)
Misc Feature(7)502..576(+)
Misc Feature(8)577..648(+)
Misc Feature(9)649..717(+)
Misc Feature(10)715..894(+)
Misc Feature(11)718..789(+)
Misc Feature(12)790..861(+)
Misc Feature(13)862..1038(+)
Misc Feature(14)862..933(+)
Misc Feature(15)934..1005(+)
Misc Feature(16)1006..>1137(+)
Misc Feature(17)1006..1071(+)
Misc Feature(18)1174..>1278(+)
Translation

Target ORF information:

RefSeq Version XM_005272632
Organism Homo sapiens (human)
Definition PREDICTED: Homo sapiens nyctalopin (NYX), transcript variant X1, mRNA.

Target ORF information:

Epitope DYKDDDDK
Bacterial selection AMPR
Mammalian selection NeoR
Vector pcDNA3.1+/C-(K)DYK
XM_005272632

ORF Insert Sequence:

1
61
121
181
241
301
361
421
481
541
601
661
721
781
841
901
961
1021
1081
1141
1201
1261
1321
1381
1441
ATGAAAGGCC GAGGGATGTT GGTCCTGCTT CTGCATGCGG TGGTCCTCGG CCTGCCCAGC 
GCCTGGGCCG TGGGGGCCTG CGCCCGCGCT TGTCCCGCCG CCTGCGCCTG CAGCACCGTG
GAGCGCGGCT GCTCGGTGCG CTGCGACCGC GCGGGCCTCC TGCGGGTGCC GGCCGAGCTC
CCGTGCGAGG CGGTCTCCAT CGACCTGGAC CGGAACGGCC TGCGCTTCCT GGGCGAGCGA
GCCTTCGGCA CGCTGCCGTC CTTGCGCCGC CTGTCGCTGC GCCACAACAA CCTGTCCTTC
ATCACGCCCG GCGCCTTCAA GGGCCTGCCG CGCCTGGCTG AGCTGCGCCT GGCGCACAAC
GGCGACCTGC GCTACCTGCA CGCGCGCACC TTCGCGGCGC TCAGCCGCCT GCGCCGCCTA
GACCTAGCAG CCTGCCGCCT CTTCAGCGTG CCCGAGCGCC TCCTGGCCGA ACTGCCGGCC
CTGCGCGAAC TCGCCGCCTT CGACAACCTG TTCCGCCGCG TGCCGGGCGC GCTGCGCGGC
CTGGCCAACC TGACGCACGC GCACCTGGAG CGCGGCCGCA TCGAGGCGGT GGCCTCCAGC
TCGCTGCAGG GCCTGCGCCG CCTGCGCTCG CTCAGCCTGC AGGCCAACCG CGTCCGTGCC
GTGCACGCTG GCGCCTTCGG GGACTGTGGC GTCCTGGAGC ATCTGCTGCT CAACGACAAC
CTGCTGGCCG AGCTCCCGGC CGACGCCTTC CGCGGCCTGC GGCGCCTGCG CACGCTCAAC
CTGGGTGGCA ACGCGCTGGA CCGCGTGGCG CGCGCCTGGT TCGCTGACCT GGCCGAGCTC
GAGCTGCTCT ACCTGGACCG CAACAGCATC GCCTTCGTGG AGGAGGGCGC CTTCCAGAAC
CTCTCGGGTC TCCTCGCGCT GCACCTCAAC GGCAACCGCC TCACCGTGCT CGCCTGGGTC
GCCTTCCAGC CCGGCTTCTT CCTGGGCCGC CTCTTCCTCT TCCGCAACCC GTGGTGCTGC
GACTGCCGTC TGGAGTGGCT GAGGGACTGG ATGGAGGGCT CCGGACGTGT CACCGACGTG
CCGTGCGCCT CCCCGGGCTC CGTGGCCGGC CTGGACCTCA GCCAGGTGAC CTTCGGGCGC
TCCTCCGATG GCCTCTGTGT GGACCCCGAG GAGCTGAACC TCACCACGTC CAGTCCAGGC
CCGTCCCCAG AACCAGCGGC CACCACCGTG AGCAGGTTCA GCAGCCTCCT CTCCAAGCTG
CTGGCCCCGA GGGTCCCGGT GGAGGAGGCG GCCAACACCA CTGGGGGGCT GGCCAACGCC
TCCCTGTCCG ACAGCCTCTC CTCCCGTGGG GTGGGAGGCG CGGGCCGGCA GCCCTGGTTT
CTCCTCGCCT CTTGTCTCCT GCCCAGCGTG GCCCAGCACG TGGTGTTTGG CCTGCAGATG
GACTGA

The stop codons will be deleted if pcDNA3.1+/C-(K)DYK vector is selected.

book

Genotype and phenotype of 101 dutch patients with congenital stationary night blindness
Ophthalmology 120 (10), 2072-2081 (2013)
Bijveld MM, Florijn RJ, Bergen AA, van den Born LI, Kamermans M, Prick L, Riemslag FC, van Schooneveld MJ, Kappers AM and van Genderen MM.


book

Electroretinographic findings in a patient with congenital stationary night blindness due to a novel NYX mutation
Ophthalmic Genet. 34 (3), 167-173 (2013)
McAnany JJ, Alexander KR, Kumar NM, Ying H, Anastasakis A and Fishman GA.


book

A novel missense mutation in the NYX gene associated with high myopia
Ophthalmic Physiol Opt 33 (3), 346-353 (2013)
Yip SP, Li CC, Yiu WC, Hung WH, Lam WW, Lai MC, Ng PW, Fung WY, Chu PH, Jiang B, Chan HH and Yap MK.


book

Mutation screening of TRPM1, GRM6, NYX and CACNA1F genes in patients with congenital stationary night blindness
Int. J. Mol. Med. 30 (3), 521-526 (2012)
Wang Q, Gao Y, Li S, Guo X and Zhang Q.


book

TRPM1 forms complexes with nyctalopin in vivo and accumulates in postsynaptic compartment of ON-bipolar neurons in mGluR6-dependent manner
J. Neurosci. 31 (32), 11521-11526 (2011)
Cao Y, Posokhova E and Martemyanov KA.


book

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), 324-327 (2000)
Pusch CM, Zeitz C, Brandau O, Pesch K, Achatz H, Feil S, Scharfe C, Maurer J, Jacobi FK, Pinckers A, Andreasson S, Hardcastle A, Wissinger B, Berger W and Meindl A.


book

Mutations in NYX, encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindness
Nat. Genet. 26 (3), 319-323 (2000)
Bech-Hansen NT, Naylor MJ, Maybaum TA, Sparkes RL, Koop B, Birch DG, Bergen AA, Prinsen CF, Polomeno RC, Gal A, Drack AV, Musarella MA, Jacobson SG, Young RS and Weleber RG.


book

Localization of CSNBX (CSNB4) between the retinitis pigmentosa loci RP2 and RP3 on proximal Xp
Invest. Ophthalmol. Vis. Sci. 38 (13), 2750-2755 (1997)
Hardcastle AJ, David-Gray ZK, Jay M, Bird AC and Bhattacharya SS.


book

X-Linked Congenital Stationary Night Blindness
(in) Pagon RA, Adam MP, Ardinger HH, Bird TD, Dolan CR, Fong CT, Smith RJH and Stephens K (Eds.); GENEREVIEWS(R); (1993)
Boycott,K.M., Sauve,Y. and MacDonald,I.M.


book

Assignment of the gene for complete X-linked congenital stationary night blindness (CSNB1) to Xp11.3
Genomics 5 (4), 727-737 (1989)
Musarella MA, Weleber RG, Murphey WH, Young RS, Anson-Cartwright L, Mets M, Kraft SP, Polemeno R, Litt M and Worton RG.


 
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