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USH1G cDNA ORF clone, Homo sapiens (human)

Gene Symbol USH1G
Entrez Gene ID 124590
Full Name Usher syndrome 1G (autosomal recessive)
Synonyms ANKS4A, SANS
General protein information
Preferred Names
Usher syndrome type-1G protein
Names
Usher syndrome type-1G protein
scaffold protein containing ankyrin repeats and SAM domain
Gene Type protein-coding
Organism Homo sapiens (human)
Genome

17

17q25.1

Summary This gene encodes a protein that contains three ankyrin domains, a class I PDZ-binding motif and a sterile alpha motif. The encoded protein interacts with harmonin, which is associated with Usher syndrome type 1C. This protein plays a role in the development and maintenance of the auditory and visual systems and functions in the cohesion of hair bundles formed by inner ear sensory cells. Mutations in this gene are associated with Usher syndrome type 1G (USH1G). Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2013]. lac of sum
Disorder MIM:

607696

Disorder Html: Usher syndrome, type 1G, 606943 (3)

mRNA and Protein(s)

mRNA Protein Name
XM_011524296 XP_011522598 Usher syndrome type-1G protein isoform X1
NM_001282489 NP_001269418 Usher syndrome type-1G protein isoform 2
NM_173477 NP_775748 Usher syndrome type-1G protein isoform 1


Homo sapiens (human) USH1G NP_775748.2
Pan troglodytes (chimpanzee) USH1G XP_523715.2
Canis lupus familiaris (dog) USH1G XP_852112.2
Bos taurus (cattle) USH1G NP_001179631.1
Mus musculus (house mouse) Ush1g NP_789817.1
Rattus norvegicus (Norway rat) Ush1g NP_001099320.1
Gallus gallus (chicken) USH1G XP_426242.2
Danio rerio (zebrafish) LOC100330314 XP_002661315.1
Drosophila melanogaster (fruit fly) Sans NP_788340.1
Xenopus (Silurana) tropicalis (western clawed frog) ush1g XP_002939606.1


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

The following USH1G gene cDNA ORF clone sequences were retrieved from the NCBI Reference Sequence Database (RefSeq). These sequences represent the protein coding region of the USH1G 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
OHu23504
XM_011524296 PREDICTED: Homo sapiens Usher syndrome 1G (autosomal recessive) (USH1G), transcript variant X1, mRNA. pcDNA3.1+/C-(K)DYK or customized vector
in pcDNA3.1+/C-(K)DYK
$159.50-$223.30
$319.00
OHu23504
NM_001282489 Homo sapiens Usher syndrome 1G (autosomal recessive) (USH1G), transcript variant 2, mRNA. pcDNA3.1+/C-(K)DYK or customized vector
in pcDNA3.1+/C-(K)DYK
$159.50-$223.30
$319.00
OHu24077
NM_173477 Homo sapiens Usher syndrome 1G (autosomal recessive) (USH1G), transcript variant 1, mRNA. pcDNA3.1+/C-(K)DYK or customized vector
in pcDNA3.1+/C-(K)DYK
$189.50-$265.30
$379.00
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 OHu23504
Clone ID Related Accession (Same CDS sequence) NM_001282489 , XM_011524296
Accession Version XM_011524296.1 Documents for ORF clone product in dufault vector
Sequence Information ORF Nucleotide Sequence (Length: 1077bp)
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 Usher syndrome type-1G protein isoform X1
Comment MODEL REFSEQ: This record is predicted by automated computational analysis. This record is derived from a genomic sequence (NT_010783.16) annotated using gene prediction method: Gnomon, supported by mRNA and EST evidence. Also see: Documentation of NCBI's Annotation Process ##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
ATGGCTGCCA TGAAGGGCCA CATGGAATGC GTGCGCTACC TGGACTCCAT CGCGGCCAAG 
CAGAGCAGCC TCAACCCCAA GCTGGTGGGT AAGCTGAAGG ACAAGGCCTT CCGCGAGGCG
GAGCGGCGCA TCCGCGAGTG CGCCAAGCTG CAGCGGAGGC ACCACGAACG CATGGAGCGG
CGATACCGGC GCGAGCTGGC CGAGCGTTCC GACACCCTCA GCTTCTCCAG CCTCACGTCC
AGCACCCTGA GCCGCCGGCT GCAGCATCTG GCGCTGGGCA GCCACCTGCC GTACTCTCAG
GCCACGCTGC ACGGCACGGC CAGGGGCAAG ACCAAGATGC AGAAGAAGCT GGAGCGGCGC
AAGCAGGGCG GCGAAGGCAC CTTCAAGGTC TCCGAGGATG GGCGCAAGAG CGCCCGCTCG
CTCTCGGGCC TGCAGCTGGG CAGCGACGTG ATGTTCGTGC GCCAGGGCAC CTACGCCAAT
CCCAAGGAGT GGGGCCGAGC CCCGCTCCGG GACATGTTCC TCTCGGACGA GGACAGCGTC
TCCCGTGCCA CGCTGGCGGC CGAGCCTGCC CACTCGGAGG TCAGCACCGA CTCAGGCCAC
GACTCCCTGT TTACCCGCCC CGGCCTGGGC ACCATGGTGT TCCGCAGAAA TTACTTGAGC
AGTGGGCTGC ACGGACTGGG CCGCGAGGAT GGGGGTCTGG ATGGGGTGGG AGCGCCGCGG
GGTCGGCTGC AGAGCTCCCC CAGCCTGGAC GATGACAGCC TGGGCAGTGC CAACAGCCTG
CAGGACCGCA GCTGTGGGGA GGAGCTGCCC TGGGATGAGC TCGATTTAGG CTTGGACGAG
GACCTGGAGC CCGAGACTAG CCCGCTGGAG ACCTTCCTGG CCTCTCTGCA CATGGAGGAC
TTTGCCGCCC TCCTGCGGCA GGAGAAGATC GACCTCGAGG CTTTGATGCT GTGCTCTGAC
CTCGACCTCC GCAGCATCAG CGTCCCACTG GGGCCCCGAA AGAAGATCTT GGGGGCCGTG
AGGAGGCGGC GGCAGGCGAT GGAGCGCCCG CCGGCCCTGG AGGACACAGA GCTATAA

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

RefSeq XP_011522598.1
CDS469..1545
Misc Feature(1)1321..1518(+)
Misc Feature(2)1321..1509(+)
Misc Feature(3)1342..1503(+)
Translation

Target ORF information:

RefSeq Version XM_011524296
Organism Homo sapiens (human)
Definition PREDICTED: Homo sapiens Usher syndrome 1G (autosomal recessive) (USH1G), transcript variant X1, mRNA.

Target ORF information:

Epitope DYKDDDDK
Bacterial selection AMPR
Mammalian selection NeoR
Vector pcDNA3.1+/C-(K)DYK
XM_011524296

ORF Insert Sequence:

1
61
121
181
241
301
361
421
481
541
601
661
721
781
841
901
961
1021
ATGGCTGCCA TGAAGGGCCA CATGGAATGC GTGCGCTACC TGGACTCCAT CGCGGCCAAG 
CAGAGCAGCC TCAACCCCAA GCTGGTGGGT AAGCTGAAGG ACAAGGCCTT CCGCGAGGCG
GAGCGGCGCA TCCGCGAGTG CGCCAAGCTG CAGCGGAGGC ACCACGAACG CATGGAGCGG
CGATACCGGC GCGAGCTGGC CGAGCGTTCC GACACCCTCA GCTTCTCCAG CCTCACGTCC
AGCACCCTGA GCCGCCGGCT GCAGCATCTG GCGCTGGGCA GCCACCTGCC GTACTCTCAG
GCCACGCTGC ACGGCACGGC CAGGGGCAAG ACCAAGATGC AGAAGAAGCT GGAGCGGCGC
AAGCAGGGCG GCGAAGGCAC CTTCAAGGTC TCCGAGGATG GGCGCAAGAG CGCCCGCTCG
CTCTCGGGCC TGCAGCTGGG CAGCGACGTG ATGTTCGTGC GCCAGGGCAC CTACGCCAAT
CCCAAGGAGT GGGGCCGAGC CCCGCTCCGG GACATGTTCC TCTCGGACGA GGACAGCGTC
TCCCGTGCCA CGCTGGCGGC CGAGCCTGCC CACTCGGAGG TCAGCACCGA CTCAGGCCAC
GACTCCCTGT TTACCCGCCC CGGCCTGGGC ACCATGGTGT TCCGCAGAAA TTACTTGAGC
AGTGGGCTGC ACGGACTGGG CCGCGAGGAT GGGGGTCTGG ATGGGGTGGG AGCGCCGCGG
GGTCGGCTGC AGAGCTCCCC CAGCCTGGAC GATGACAGCC TGGGCAGTGC CAACAGCCTG
CAGGACCGCA GCTGTGGGGA GGAGCTGCCC TGGGATGAGC TCGATTTAGG CTTGGACGAG
GACCTGGAGC CCGAGACTAG CCCGCTGGAG ACCTTCCTGG CCTCTCTGCA CATGGAGGAC
TTTGCCGCCC TCCTGCGGCA GGAGAAGATC GACCTCGAGG CTTTGATGCT GTGCTCTGAC
CTCGACCTCC GCAGCATCAG CGTCCCACTG GGGCCCCGAA AGAAGATCTT GGGGGCCGTG
AGGAGGCGGC GGCAGGCGAT GGAGCGCCCG CCGGCCCTGG AGGACACAGA GCTATAA

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

CloneID OHu23504
Clone ID Related Accession (Same CDS sequence) NM_001282489 , XM_011524296
Accession Version NM_001282489.2 Documents for ORF clone product in dufault vector
Sequence Information ORF Nucleotide Sequence (Length: 1077bp)
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 15-MAR-2015
Organism Homo sapiens (human)
Product Usher syndrome type-1G protein isoform 2
Comment REVIEWED REFSEQ: This record has been curated by NCBI staff. The reference sequence was derived from DC403891.1, AK296899.1, BC101096.2 and AC087651.19. On Mar 25, 2014 this sequence version replaced gi:542133067. Transcript Variant: This variant (2) differs in its 5' UTR and initiates translation at a downstream start codon, compared to variant 1. The encoded isoform (2) is shorter, compared to isoform 1. Sequence Note: This RefSeq record was created from transcript and genomic sequence data to make the sequence consistent with the reference genome assembly. The genomic coordinates used for the transcript record were based on transcript alignments. 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 :: AK296899.1 [ECO:0000332] RNAseq introns :: mixed/partial sample support SAMEA2148093 [ECO:0000350] ##Evidence-Data-END##

1
61
121
181
241
301
361
421
481
541
601
661
721
781
841
901
961
1021
ATGGCTGCCA TGAAGGGCCA CATGGAATGC GTGCGCTACC TGGACTCCAT CGCGGCCAAG 
CAGAGCAGCC TCAACCCCAA GCTGGTGGGT AAGCTGAAGG ACAAGGCCTT CCGCGAGGCG
GAGCGGCGCA TCCGCGAGTG CGCCAAGCTG CAGCGGAGGC ACCACGAACG CATGGAGCGG
CGATACCGGC GCGAGCTGGC CGAGCGTTCC GACACCCTCA GCTTCTCCAG CCTCACGTCC
AGCACCCTGA GCCGCCGGCT GCAGCATCTG GCGCTGGGCA GCCACCTGCC GTACTCTCAG
GCCACGCTGC ACGGCACGGC CAGGGGCAAG ACCAAGATGC AGAAGAAGCT GGAGCGGCGC
AAGCAGGGCG GCGAAGGCAC CTTCAAGGTC TCCGAGGATG GGCGCAAGAG CGCCCGCTCG
CTCTCGGGCC TGCAGCTGGG CAGCGACGTG ATGTTCGTGC GCCAGGGCAC CTACGCCAAT
CCCAAGGAGT GGGGCCGAGC CCCGCTCCGG GACATGTTCC TCTCGGACGA GGACAGCGTC
TCCCGTGCCA CGCTGGCGGC CGAGCCTGCC CACTCGGAGG TCAGCACCGA CTCAGGCCAC
GACTCCCTGT TTACCCGCCC CGGCCTGGGC ACCATGGTGT TCCGCAGAAA TTACTTGAGC
AGTGGGCTGC ACGGACTGGG CCGCGAGGAT GGGGGTCTGG ATGGGGTGGG AGCGCCGCGG
GGTCGGCTGC AGAGCTCCCC CAGCCTGGAC GATGACAGCC TGGGCAGTGC CAACAGCCTG
CAGGACCGCA GCTGTGGGGA GGAGCTGCCC TGGGATGAGC TCGATTTAGG CTTGGACGAG
GACCTGGAGC CCGAGACTAG CCCGCTGGAG ACCTTCCTGG CCTCTCTGCA CATGGAGGAC
TTTGCCGCCC TCCTGCGGCA GGAGAAGATC GACCTCGAGG CTTTGATGCT GTGCTCTGAC
CTCGACCTCC GCAGCATCAG CGTCCCACTG GGGCCCCGAA AGAAGATCTT GGGGGCCGTG
AGGAGGCGGC GGCAGGCGAT GGAGCGCCCG CCGGCCCTGG AGGACACAGA GCTATAA

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

RefSeq NP_001269418.1
CDS447..1523
Misc Feature(1)345..347(+)
Misc Feature(2)1299..1496(+)
Misc Feature(3)1299..1487(+)
Misc Feature(4)1320..1481(+)
Exon (1)1..354
Gene:USH1G
Gene Synonym:
Exon (2)355..1519
Gene:USH1G
Gene Synonym:
Exon (3)1520..3512
Gene:USH1G
Gene Synonym:
Translation

Target ORF information:

RefSeq Version NM_001282489
Organism Homo sapiens (human)
Definition Homo sapiens Usher syndrome 1G (autosomal recessive) (USH1G), transcript variant 2, mRNA.

Target ORF information:

Epitope DYKDDDDK
Bacterial selection AMPR
Mammalian selection NeoR
Vector pcDNA3.1+/C-(K)DYK
NM_001282489

ORF Insert Sequence:

1
61
121
181
241
301
361
421
481
541
601
661
721
781
841
901
961
1021
ATGGCTGCCA TGAAGGGCCA CATGGAATGC GTGCGCTACC TGGACTCCAT CGCGGCCAAG 
CAGAGCAGCC TCAACCCCAA GCTGGTGGGT AAGCTGAAGG ACAAGGCCTT CCGCGAGGCG
GAGCGGCGCA TCCGCGAGTG CGCCAAGCTG CAGCGGAGGC ACCACGAACG CATGGAGCGG
CGATACCGGC GCGAGCTGGC CGAGCGTTCC GACACCCTCA GCTTCTCCAG CCTCACGTCC
AGCACCCTGA GCCGCCGGCT GCAGCATCTG GCGCTGGGCA GCCACCTGCC GTACTCTCAG
GCCACGCTGC ACGGCACGGC CAGGGGCAAG ACCAAGATGC AGAAGAAGCT GGAGCGGCGC
AAGCAGGGCG GCGAAGGCAC CTTCAAGGTC TCCGAGGATG GGCGCAAGAG CGCCCGCTCG
CTCTCGGGCC TGCAGCTGGG CAGCGACGTG ATGTTCGTGC GCCAGGGCAC CTACGCCAAT
CCCAAGGAGT GGGGCCGAGC CCCGCTCCGG GACATGTTCC TCTCGGACGA GGACAGCGTC
TCCCGTGCCA CGCTGGCGGC CGAGCCTGCC CACTCGGAGG TCAGCACCGA CTCAGGCCAC
GACTCCCTGT TTACCCGCCC CGGCCTGGGC ACCATGGTGT TCCGCAGAAA TTACTTGAGC
AGTGGGCTGC ACGGACTGGG CCGCGAGGAT GGGGGTCTGG ATGGGGTGGG AGCGCCGCGG
GGTCGGCTGC AGAGCTCCCC CAGCCTGGAC GATGACAGCC TGGGCAGTGC CAACAGCCTG
CAGGACCGCA GCTGTGGGGA GGAGCTGCCC TGGGATGAGC TCGATTTAGG CTTGGACGAG
GACCTGGAGC CCGAGACTAG CCCGCTGGAG ACCTTCCTGG CCTCTCTGCA CATGGAGGAC
TTTGCCGCCC TCCTGCGGCA GGAGAAGATC GACCTCGAGG CTTTGATGCT GTGCTCTGAC
CTCGACCTCC GCAGCATCAG CGTCCCACTG GGGCCCCGAA AGAAGATCTT GGGGGCCGTG
AGGAGGCGGC GGCAGGCGAT GGAGCGCCCG CCGGCCCTGG AGGACACAGA GCTATAA

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

CloneID OHu24077
Clone ID Related Accession (Same CDS sequence) NM_173477
Accession Version NM_173477.4 Documents for ORF clone product in dufault vector
Sequence Information ORF Nucleotide Sequence (Length: 1386bp)
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 15-MAR-2015
Organism Homo sapiens (human)
Product Usher syndrome type-1G protein isoform 1
Comment REVIEWED REFSEQ: This record has been curated by NCBI staff. The reference sequence was derived from DC403891.1, BC101096.2 and AC087651.19. On Mar 25, 2014 this sequence version replaced gi:542133066. Transcript Variant: This variant (1) represents the longer transcript and encodes the longer isoform (1). Sequence Note: This RefSeq record was created from transcript and genomic sequence data to make the sequence consistent with the reference genome assembly. The genomic coordinates used for the transcript record were based on transcript alignments. 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 :: AK091243.1, AK289804.1 [ECO:0000332] RNAseq introns :: single sample supports all introns SAMEA2148093 [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
1381
ATGAACGACC AGTACCACCG GGCAGCCCGG GATGGCTACC TGGAGCTCCT CAAGGAGGCC 
ACCCGAAAGG AGCTGAATGC CCCCGACGAG GATGGCATGA CCCCCACTCT CTGGGCTGCC
TACCATGGCA ACCTCGAGTC GCTGCGTCTC ATTGTGAGCC GCGGGGGTGA CCCGGACAAG
TGTGACATCT GGGGCAACAC ACCCCTGCAT CTGGCAGCTT CCAATGGCCA CTTGCACTGC
CTGTCCTTCC TGGTGTCCTT CGGAGCCAAC ATCTGGTGCC TAGACAACGA CTACCACACG
CCGCTGGACA TGGCTGCCAT GAAGGGCCAC ATGGAATGCG TGCGCTACCT GGACTCCATC
GCGGCCAAGC AGAGCAGCCT CAACCCCAAG CTGGTGGGTA AGCTGAAGGA CAAGGCCTTC
CGCGAGGCGG AGCGGCGCAT CCGCGAGTGC GCCAAGCTGC AGCGGAGGCA CCACGAACGC
ATGGAGCGGC GATACCGGCG CGAGCTGGCC GAGCGTTCCG ACACCCTCAG CTTCTCCAGC
CTCACGTCCA GCACCCTGAG CCGCCGGCTG CAGCATCTGG CGCTGGGCAG CCACCTGCCG
TACTCTCAGG CCACGCTGCA CGGCACGGCC AGGGGCAAGA CCAAGATGCA GAAGAAGCTG
GAGCGGCGCA AGCAGGGCGG CGAAGGCACC TTCAAGGTCT CCGAGGATGG GCGCAAGAGC
GCCCGCTCGC TCTCGGGCCT GCAGCTGGGC AGCGACGTGA TGTTCGTGCG CCAGGGCACC
TACGCCAATC CCAAGGAGTG GGGCCGAGCC CCGCTCCGGG ACATGTTCCT CTCGGACGAG
GACAGCGTCT CCCGTGCCAC GCTGGCGGCC GAGCCTGCCC ACTCGGAGGT CAGCACCGAC
TCAGGCCACG ACTCCCTGTT TACCCGCCCC GGCCTGGGCA CCATGGTGTT CCGCAGAAAT
TACTTGAGCA GTGGGCTGCA CGGACTGGGC CGCGAGGATG GGGGTCTGGA TGGGGTGGGA
GCGCCGCGGG GTCGGCTGCA GAGCTCCCCC AGCCTGGACG ATGACAGCCT GGGCAGTGCC
AACAGCCTGC AGGACCGCAG CTGTGGGGAG GAGCTGCCCT GGGATGAGCT CGATTTAGGC
TTGGACGAGG ACCTGGAGCC CGAGACTAGC CCGCTGGAGA CCTTCCTGGC CTCTCTGCAC
ATGGAGGACT TTGCCGCCCT CCTGCGGCAG GAGAAGATCG ACCTCGAGGC TTTGATGCTG
TGCTCTGACC TCGACCTCCG CAGCATCAGC GTCCCACTGG GGCCCCGAAA GAAGATCTTG
GGGGCCGTGA GGAGGCGGCG GCAGGCGATG GAGCGCCCGC CGGCCCTGGA GGACACAGAG
CTATAA

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

RefSeq NP_775748.2
CDS191..1576
Misc Feature(1)20..22(+)
Misc Feature(2)206..541(+)
Misc Feature(3)206..463(+)
Misc Feature(4)281..370(+)
Misc Feature(5)380..469(+)
Misc Feature(6)395..>541(+)
Misc Feature(7)479..568(+)
Misc Feature(8)1352..1549(+)
Misc Feature(9)1352..1540(+)
Misc Feature(10)1373..1534(+)
Exon (1)1..354
Gene:USH1G
Gene Synonym:
Exon (2)355..1572
Gene:USH1G
Gene Synonym:
Exon (3)1573..3565
Gene:USH1G
Gene Synonym:
Translation

Target ORF information:

RefSeq Version NM_173477
Organism Homo sapiens (human)
Definition Homo sapiens Usher syndrome 1G (autosomal recessive) (USH1G), transcript variant 1, mRNA.

Target ORF information:

Epitope DYKDDDDK
Bacterial selection AMPR
Mammalian selection NeoR
Vector pcDNA3.1+/C-(K)DYK
NM_173477

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
ATGAACGACC AGTACCACCG GGCAGCCCGG GATGGCTACC TGGAGCTCCT CAAGGAGGCC 
ACCCGAAAGG AGCTGAATGC CCCCGACGAG GATGGCATGA CCCCCACTCT CTGGGCTGCC
TACCATGGCA ACCTCGAGTC GCTGCGTCTC ATTGTGAGCC GCGGGGGTGA CCCGGACAAG
TGTGACATCT GGGGCAACAC ACCCCTGCAT CTGGCAGCTT CCAATGGCCA CTTGCACTGC
CTGTCCTTCC TGGTGTCCTT CGGAGCCAAC ATCTGGTGCC TAGACAACGA CTACCACACG
CCGCTGGACA TGGCTGCCAT GAAGGGCCAC ATGGAATGCG TGCGCTACCT GGACTCCATC
GCGGCCAAGC AGAGCAGCCT CAACCCCAAG CTGGTGGGTA AGCTGAAGGA CAAGGCCTTC
CGCGAGGCGG AGCGGCGCAT CCGCGAGTGC GCCAAGCTGC AGCGGAGGCA CCACGAACGC
ATGGAGCGGC GATACCGGCG CGAGCTGGCC GAGCGTTCCG ACACCCTCAG CTTCTCCAGC
CTCACGTCCA GCACCCTGAG CCGCCGGCTG CAGCATCTGG CGCTGGGCAG CCACCTGCCG
TACTCTCAGG CCACGCTGCA CGGCACGGCC AGGGGCAAGA CCAAGATGCA GAAGAAGCTG
GAGCGGCGCA AGCAGGGCGG CGAAGGCACC TTCAAGGTCT CCGAGGATGG GCGCAAGAGC
GCCCGCTCGC TCTCGGGCCT GCAGCTGGGC AGCGACGTGA TGTTCGTGCG CCAGGGCACC
TACGCCAATC CCAAGGAGTG GGGCCGAGCC CCGCTCCGGG ACATGTTCCT CTCGGACGAG
GACAGCGTCT CCCGTGCCAC GCTGGCGGCC GAGCCTGCCC ACTCGGAGGT CAGCACCGAC
TCAGGCCACG ACTCCCTGTT TACCCGCCCC GGCCTGGGCA CCATGGTGTT CCGCAGAAAT
TACTTGAGCA GTGGGCTGCA CGGACTGGGC CGCGAGGATG GGGGTCTGGA TGGGGTGGGA
GCGCCGCGGG GTCGGCTGCA GAGCTCCCCC AGCCTGGACG ATGACAGCCT GGGCAGTGCC
AACAGCCTGC AGGACCGCAG CTGTGGGGAG GAGCTGCCCT GGGATGAGCT CGATTTAGGC
TTGGACGAGG ACCTGGAGCC CGAGACTAGC CCGCTGGAGA CCTTCCTGGC CTCTCTGCAC
ATGGAGGACT TTGCCGCCCT CCTGCGGCAG GAGAAGATCG ACCTCGAGGC TTTGATGCTG
TGCTCTGACC TCGACCTCCG CAGCATCAGC GTCCCACTGG GGCCCCGAAA GAAGATCTTG
GGGGCCGTGA GGAGGCGGCG GCAGGCGATG GAGCGCCCGC CGGCCCTGGA GGACACAGAG
CTATAA

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

 
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