| Gene Symbol | Nyx |
| Entrez Gene ID | 302516 |
| Full Name | nyctalopin |
| Synonyms | RGD1561300 |
| General protein information |
|
| Gene Type | protein-coding |
| Organism | Rattus norvegicus(Norway rat) |
| Genome |
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Nyx cDNA ORF clone, Rattus norvegicus(Norway rat)
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Gene
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Clones
gRNAs
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.
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Reference Sequences (Refseq)
CloneID ORa00433 Clone ID Related Accession (Same CDS sequence) NM_001100967.1 Accession Version NM_001100967.1 Latest version! Documents for ORF clone product in default vector Sequence Information ORF Nucleotide Sequence (Length: 1431bp)
Protein sequence
SNPVector pcDNA3.1-C-(k)DYK or customized vector 
User ManualClone information Clone Map MSDSTag on pcDNA3.1+/C-(K)DYK C terminal DYKDDDDK tags ORF Insert Method CloneEZ™ Seamless cloning technology Insert Structure linear Update Date 1527350400000 Organism Rattus norvegicus(Norway rat) Product nyctalopin precursor Comment Comment: PROVISIONAL REFSEQ: This record has not yet been subject to final NCBI review. The reference sequence was derived from DQ393414.1. On or before Aug 12, 2007 this sequence version replaced XM_228750.4, XM_001060061.1. ##Evidence-Data-START## Transcript exon combination :: DQ393414.1 [ECO:0000332] RNAseq introns :: single sample supports all introns SAMD00052296, SAMD00052297 [ECO:0000348] ##Evidence-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
1381ATGCTGAACC TGCTTCTTTA TGCGGTGGTC TTCAGCCTGC CCTGCACCCG GGCCACCGAG
GCCTGTCTGC GGGCCTGCCC TGCGGCCTGC ACTTGCAGTA ACGTGGAGCG TGGCTGCTCA
GTGCGCTGTG ACCGTGCGGG CCTCCAGCGG GTGCCCACTG AGTTTCCGTG TGAGGCGGCC
TCCATCGACC TAGACCGGAA TGGGTTGCGC ATCCTGGGCG AGCGGGCCTT TGGCACGCTG
CCATCGTTAC GCTGCCTGTC GCTGCGCCAC AACAACCTGT CCTTTATTAC GCCTGGCGCC
TTCAAGGGCC TGCCGCGGTT GGCCGAGCTG CGCCTGGCGC ACAATGGTGA GCTACGCTAT
CTGCACGTGC GGACCTTCGC GGCGCTGGGT CGCCTGCGCC GCCTGGACCT GGCGGCCTGC
CGCCTCTTCA GCGTGCCCGA GCGTCTCCTG GCCGAGCTGC CGGCCCTGCG TGAGCTCACG
GCCTTCGACA ATCTCTTCCG CCGGGTGCCC GGCGCGCTCC GTGGCCTGGC TAACCTGACG
CACGCGCATT TCGAGCGCAG CCGCATCGAG GCTGTGGCCT CCAGCTCGCT GCTGGGCATG
CGGCGTCTGC GCTCGCTCAG CCTGCAGGCC AACCGCGTGC GCGCAGTGCA TGCCGGGGCC
TTTGGCGACT GCGTGGCCCT GGAGCACCTG CTGCTCAACG ATAACCTGCT GGCCTCGCTG
CCTGCCGCCG CCTTCCGCGG CCTTCGCCGC CTGCGCACCC TCAATCTGGG CGGCAACGCG
TTGGGCAGCG TGGCGCGCGG CTGGTTCTCC GACCTGGCAG AGCTCGAGCT GCTTTACCTA
GATCGCAACA GCATCACCTT TGTGGAGGAA GGCGCCTTCC AGAACCTCTC GGGCCTCCTG
GCCCTGCATC TCAATGGCAA CCGCCTCACT GTGCTCTCCT GGGCCGCTTT CCAGCCAGGC
TTCTTCCTGG GCCGCCTTTT TCTCTTCCGC AACCCTTGGC GCTGTGACTG CCACCTGGAG
TGGTTGCGTG ATTGGATGGA GGGCTCTGGG CGTGTGGCTG ATGTGGCATG CGCCTCCCCT
GGCTCTGTGG CCGGCCAGGA CCTCAGCCAG GTGGTCTTTG AGCGCTCCTC TGATGGCATC
TGTGTGGACC CTGATGAGCT GAACTTCACC ACGTTCAGTC CAGGCCCGAG TCCAGAGCCA
GTGGCCACCA CTGTGAGCAG ATTCAGCAGC CTCCTCTCCA AGCTGCTGGC CCCAAGGGCC
CCTGTGGAGG AGGTAGCCAA CACCACCTGG GAGCTGGTCA ATGTCTCCTT GAATGACAGT
TTTCGGTCCC ATGGAGTGAT GGTCATGTGC TACAAGGCCA CGTTTCTCTT CACTTCTTGC
CTCTGGCTCA GCCTGGCCCA GTATGTGGTG TTGGGTCCAC AGAGGGACTG AThe stop codons will be deleted if pcDNA3.1+/C-(K)DYK vector is selected.
RefSeq NP_001094437.1 CDS 202..1632 Translation 
Target ORF information:
RefSeq Version NM_001100967.1 Organism Rattus norvegicus(Norway rat) Definition Rattus norvegicus nyctalopin (Nyx), mRNA. Target ORF information:
Epitope DYKDDDDK Bacterial selection AMPR Mammalian selection NeoR Vector pcDNA3.1+/C-(K)DYK 
NM_001100967.1
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
1381ATGCTGAACC TGCTTCTTTA TGCGGTGGTC TTCAGCCTGC CCTGCACCCG GGCCACCGAG
GCCTGTCTGC GGGCCTGCCC TGCGGCCTGC ACTTGCAGTA ACGTGGAGCG TGGCTGCTCA
GTGCGCTGTG ACCGTGCGGG CCTCCAGCGG GTGCCCACTG AGTTTCCGTG TGAGGCGGCC
TCCATCGACC TAGACCGGAA TGGGTTGCGC ATCCTGGGCG AGCGGGCCTT TGGCACGCTG
CCATCGTTAC GCTGCCTGTC GCTGCGCCAC AACAACCTGT CCTTTATTAC GCCTGGCGCC
TTCAAGGGCC TGCCGCGGTT GGCCGAGCTG CGCCTGGCGC ACAATGGTGA GCTACGCTAT
CTGCACGTGC GGACCTTCGC GGCGCTGGGT CGCCTGCGCC GCCTGGACCT GGCGGCCTGC
CGCCTCTTCA GCGTGCCCGA GCGTCTCCTG GCCGAGCTGC CGGCCCTGCG TGAGCTCACG
GCCTTCGACA ATCTCTTCCG CCGGGTGCCC GGCGCGCTCC GTGGCCTGGC TAACCTGACG
CACGCGCATT TCGAGCGCAG CCGCATCGAG GCTGTGGCCT CCAGCTCGCT GCTGGGCATG
CGGCGTCTGC GCTCGCTCAG CCTGCAGGCC AACCGCGTGC GCGCAGTGCA TGCCGGGGCC
TTTGGCGACT GCGTGGCCCT GGAGCACCTG CTGCTCAACG ATAACCTGCT GGCCTCGCTG
CCTGCCGCCG CCTTCCGCGG CCTTCGCCGC CTGCGCACCC TCAATCTGGG CGGCAACGCG
TTGGGCAGCG TGGCGCGCGG CTGGTTCTCC GACCTGGCAG AGCTCGAGCT GCTTTACCTA
GATCGCAACA GCATCACCTT TGTGGAGGAA GGCGCCTTCC AGAACCTCTC GGGCCTCCTG
GCCCTGCATC TCAATGGCAA CCGCCTCACT GTGCTCTCCT GGGCCGCTTT CCAGCCAGGC
TTCTTCCTGG GCCGCCTTTT TCTCTTCCGC AACCCTTGGC GCTGTGACTG CCACCTGGAG
TGGTTGCGTG ATTGGATGGA GGGCTCTGGG CGTGTGGCTG ATGTGGCATG CGCCTCCCCT
GGCTCTGTGG CCGGCCAGGA CCTCAGCCAG GTGGTCTTTG AGCGCTCCTC TGATGGCATC
TGTGTGGACC CTGATGAGCT GAACTTCACC ACGTTCAGTC CAGGCCCGAG TCCAGAGCCA
GTGGCCACCA CTGTGAGCAG ATTCAGCAGC CTCCTCTCCA AGCTGCTGGC CCCAAGGGCC
CCTGTGGAGG AGGTAGCCAA CACCACCTGG GAGCTGGTCA ATGTCTCCTT GAATGACAGT
TTTCGGTCCC ATGGAGTGAT GGTCATGTGC TACAAGGCCA CGTTTCTCTT CACTTCTTGC
CTCTGGCTCA GCCTGGCCCA GTATGTGGTG TTGGGTCCAC AGAGGGACTG AThe stop codons will be deleted if pcDNA3.1+/C-(K)DYK vector is selected.
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PubMed
A naturally-occurring mutation in Cacna1f in a rat model of congenital stationary night blindness.
Molecular vision1420-8(2008 Jan)
Gu Y,Wang L,Zhou J,Guo Q,Liu N,Ding Z,Li L,Liu X,An J,Yan G,Yao L,Zhang Z
Contribution of Kir4.1 to the mouse electroretinogram.
Molecular vision10650-4(2004 Sep)
Wu J,Marmorstein AD,Kofuji P,Peachey NS
Identification of the gene and the mutation responsible for the mouse nob phenotype.
Investigative ophthalmology & visual science44(1)378-84(2003 Jan)
Gregg RG,Mukhopadhyay S,Candille SI,Ball SL,Pardue MT,McCall MA,Peachey NS
Mutations in NYX, encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindness.
Nature genetics26(3)319-23(2000 Nov)
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,Weleber RG
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