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MKS1 cDNA ORF clone, Homo sapiens (human)

Gene Symbol MKS1
Entrez Gene ID 54903
Full Name Meckel syndrome, type 1
Synonyms BBS13, MES, MKS, POC12
General protein information
Preferred Names
Meckel syndrome type 1 protein
Names
Meckel syndrome type 1 protein
FABB proteome-like protein
POC12 centriolar protein homolog
Gene Type protein-coding
Organism Homo sapiens (human)
Genome

17

17q22

Summary The protein encoded by this gene localizes to the basal body and is required for formation of the primary cilium in ciliated epithelial cells. Mutations in this gene result in Meckel syndrome type 1 and in Bardet-Biedl syndrome type 13. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2009]. lac of sum
Disorder MIM:

609883

Disorder Html: Meckel syndrome, type 1, 249000 (3); Bardet-Biedl syndrome 13,

mRNA and Protein(s)

mRNA Protein Name
XM_011524957 XP_011523259 Meckel syndrome type 1 protein isoform X1
XM_011524958 XP_011523260 Meckel syndrome type 1 protein isoform X2
XM_005257483 XP_005257540 Meckel syndrome type 1 protein isoform X3
XM_011524959 XP_011523261 Meckel syndrome type 1 protein isoform X4
XM_011524960 XP_011523262 Meckel syndrome type 1 protein isoform X5
XM_005257485 XP_005257542 Meckel syndrome type 1 protein isoform X6
XM_006721965 XP_006722028 Meckel syndrome type 1 protein isoform X7
XM_005257486 XP_005257543 Meckel syndrome type 1 protein isoform X8
NM_017777 NP_060247 Meckel syndrome type 1 protein isoform 1
NM_001165927 NP_001159399 Meckel syndrome type 1 protein isoform 2



Homo sapiens (human) MKS1 NP_060247.2
Pan troglodytes (chimpanzee) MKS1 XP_001172592.1
Canis lupus familiaris (dog) MKS1 XP_003639341.1
Bos taurus (cattle) LOC101905689 XP_005220007.1
Mus musculus (house mouse) Mks1 NP_001034773.2
Rattus norvegicus (Norway rat) Mks1 NP_001030089.2
Gallus gallus (chicken) MKS1 XP_415705.3
Danio rerio (zebrafish) mks1 NP_001070841.2
Xenopus (Silurana) tropicalis (western clawed frog) mks1 NP_001039150.1


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

The following MKS1 gene cDNA ORF clone sequences were retrieved from the NCBI Reference Sequence Database (RefSeq). These sequences represent the protein coding region of the MKS1 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
OHu68758 XM_011524957 PREDICTED: Homo sapiens Meckel syndrome, type 1 (MKS1), transcript variant X1, mRNA. pcDNA3.1+/C-(K)DYK or customized vector 7-9 $307.30
$439.00
OHu68759 XM_011524958 PREDICTED: Homo sapiens Meckel syndrome, type 1 (MKS1), transcript variant X2, mRNA. pcDNA3.1+/C-(K)DYK or customized vector 7-9 $307.30
$439.00
OHu50503 XM_005257483 PREDICTED: Homo sapiens Meckel syndrome, type 1 (MKS1), transcript variant X3, mRNA. pcDNA3.1+/C-(K)DYK or customized vector 7-9 $307.30
$439.00
OHu68760 XM_011524959 PREDICTED: Homo sapiens Meckel syndrome, type 1 (MKS1), transcript variant X4, mRNA. pcDNA3.1+/C-(K)DYK or customized vector 7-9 $223.30
$319.00
OHu68761 XM_011524960 PREDICTED: Homo sapiens Meckel syndrome, type 1 (MKS1), transcript variant X5, mRNA. pcDNA3.1+/C-(K)DYK or customized vector 7-9 $223.30
$319.00
OHu50506 XM_005257485 PREDICTED: Homo sapiens Meckel syndrome, type 1 (MKS1), transcript variant X6, mRNA. pcDNA3.1+/C-(K)DYK or customized vector 7-9 $223.30
$319.00
OHu50507 XM_006721965 PREDICTED: Homo sapiens Meckel syndrome, type 1 (MKS1), transcript variant X7, mRNA. pcDNA3.1+/C-(K)DYK or customized vector 7-9 $223.30
$319.00
OHu50508 XM_005257486 PREDICTED: Homo sapiens Meckel syndrome, type 1 (MKS1), transcript variant X8, mRNA. pcDNA3.1+/C-(K)DYK or customized vector 5-7 $223.30
$319.00
OHu26205
NM_017777 Homo sapiens Meckel syndrome, type 1 (MKS1), transcript variant 1, mRNA. pcDNA3.1+/C-(K)DYK or customized vector
in pcDNA3.1+/C-(K)DYK
$234.50-$328.30
$469.00
OHu26353 NM_001165927 Homo sapiens Meckel syndrome, type 1 (MKS1), transcript variant 2, mRNA. pcDNA3.1+/C-(K)DYK or customized vector 7-9 $307.30
$439.00
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 OHu68758
Clone ID Related Accession (Same CDS sequence) XM_011524957
Accession Version XM_011524957.1 Documents for ORF clone product in dufault vector
Sequence Information ORF Nucleotide Sequence (Length: 1695bp)
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
ORF Insert Method CloneEZ® Seamless cloning technology
Structure linear
Update Date 12-MAR-2015
Organism Homo sapiens (human)
Product Meckel syndrome type 1 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 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
1081
1141
1201
1261
1321
1381
1441
1501
1561
1621
1681
ATGGCGGAGA CCGTCTGGAG CACTGACACC GGGGAGGCAG TGTATCGCTC CCGGGACCCC 
GTGCGCAACT TGCGCCTCCG AGTCCACCTG CAAAGAATCA CATCAAGCAA CTTTCTTCAT
TATCAGCCTG CTGCCGAGCT CGGGAAGGAC CTCATAGACT TGGCCACTTT TAGGCCTCAG
CCAACTGCCA TCTTTGGAGG TGGACACCGC CCAGAGGAAG ACGAAGAGGA GGAGATTGTG
ATTGGGTGGC AGGAGAAGCT CTTTAGCCAG TTTGAAGTAG ATCTGTACCA AAATGAAACA
GCCTGTCAGA GTCCTTTGGA TTATCAGTAC CGTCAGGAGA TCCTGAAGCT GGAGAATTCG
GGTGGCAAGA AAAACCGACG AATCTTTACC TACACTGACT CTGATAGATA CACCAATTTG
GAGGAGCACT GTCAGAGAAT GACCACTGCA GCCAGCGAGG TGCCTTCATT CTTGGTCGAG
CGAATGGCAA ATGTCAGGCG TCGCCGGCAG GACAGGCGAG GGATGGAGGG CGGCATCCTC
AAGTCACGCA TCGTCACCTG GGAGCCCTCA GAAGAGTTTG TCAGGAACAA CCACGTCATT
AACACCCCTC TTCAGACAAT GCACATCATG GCAGACCTGG GGCCCTATAA AAAGCTTGGC
TATAAGAAGT ATGAACATGT CCTGTGTACT CTGAAGGTGG ATAGCAATGG TGTGATCACA
GTAAAGCCTG ACTTCACGGG CCTCAAAGGA CCCTACAGGA TTGAGACGGA GGGGGAGAAG
CAGGAGCTGT GGAAATATAC GATCGACAAT GTTTCCCCCC ACGCACAGCC GGAGGAGGAG
GAGCGGGAAC GGCGAGTGTT CAAGGATCTT TATGGCCGGC ACAAGGAGTA TCTCAGCAGC
CTCGTAGGCA CCGACTTTGA GATGACTGTC CCAGGTGCCC TCCGGCTCTT TGTAAATGGA
GAGGTCGTTT CAGCCCAAGG CTATGAGTAT GACAATCTCT ACGTCCACTT CTTTGTAGAA
TTGCCAACTG CTCACTGGTC AAGCCCAGCA TTCCAGCAGC TCTCAGGAGT AACACAGACC
TGCACCACCA AGTCCCTGGC AATGGACAAG GTGGCTCACT TCTCCTACCC ATTCACGTTT
GAAGCCTTCT TCCTCCATGA GGATGAATCT TCTGATGCAC TCCCGGAGTG GCCTGTGCTC
TACTGTGAGG TCCTCTCGCT GGACTTCTGG CAGAGGTACC GTGTGGAAGG CTATGGGGCT
GTGGTGCTGC CTGCCACTCC AGGCTCACAC ACCCTGACAG TCTCCACGTG GAGACCTGTG
GAGCTTGGCA CGGTGGCTGA GCTGAGGAGG TTTTTCATTG GCGGTTCTCT GGAACTGGAG
GACCTCTCCT ATGTACGGAT ACCAGGATCC TTCAAGGGCC TTCATGGAAT CGAGCTCCCT
TCAGAAAAGG ATGCGGAGTG TGTTGGACCG TCTGGAAGGG TTCAGCCAGC AGAGTTCCAT
TCACAATGTG CTAGAGGCCT TCCGTCGAGC CCGGCGCCGC ATGCAGGAGG CCCGGGAAAG
CCTCCCGCAG GACCTAGTGA GCCCCTCTGG AACCCTGGTC TCCTAGCTCA CAGCAGCCCT
GGCCCACAGT GCAAGAGGAC AAGATGGGGG ATATCTGAGG CCAGTGCTCT CCTGCCTCTT
CGTCTTTCTG ATTAG

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

RefSeq XP_011523259.1
CDS49..1743
Misc Feature(1)991..1473(+)
Translation

Target ORF information:

RefSeq Version XM_011524957
Organism Homo sapiens (human)
Definition PREDICTED: Homo sapiens Meckel syndrome, type 1 (MKS1), transcript variant X1, mRNA.

Target ORF information:

Epitope DYKDDDDK
Bacterial selection AMPR
Mammalian selection NeoR
Vector pcDNA3.1+/C-(K)DYK
XM_011524957

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
1501
1561
1621
1681
ATGGCGGAGA CCGTCTGGAG CACTGACACC GGGGAGGCAG TGTATCGCTC CCGGGACCCC 
GTGCGCAACT TGCGCCTCCG AGTCCACCTG CAAAGAATCA CATCAAGCAA CTTTCTTCAT
TATCAGCCTG CTGCCGAGCT CGGGAAGGAC CTCATAGACT TGGCCACTTT TAGGCCTCAG
CCAACTGCCA TCTTTGGAGG TGGACACCGC CCAGAGGAAG ACGAAGAGGA GGAGATTGTG
ATTGGGTGGC AGGAGAAGCT CTTTAGCCAG TTTGAAGTAG ATCTGTACCA AAATGAAACA
GCCTGTCAGA GTCCTTTGGA TTATCAGTAC CGTCAGGAGA TCCTGAAGCT GGAGAATTCG
GGTGGCAAGA AAAACCGACG AATCTTTACC TACACTGACT CTGATAGATA CACCAATTTG
GAGGAGCACT GTCAGAGAAT GACCACTGCA GCCAGCGAGG TGCCTTCATT CTTGGTCGAG
CGAATGGCAA ATGTCAGGCG TCGCCGGCAG GACAGGCGAG GGATGGAGGG CGGCATCCTC
AAGTCACGCA TCGTCACCTG GGAGCCCTCA GAAGAGTTTG TCAGGAACAA CCACGTCATT
AACACCCCTC TTCAGACAAT GCACATCATG GCAGACCTGG GGCCCTATAA AAAGCTTGGC
TATAAGAAGT ATGAACATGT CCTGTGTACT CTGAAGGTGG ATAGCAATGG TGTGATCACA
GTAAAGCCTG ACTTCACGGG CCTCAAAGGA CCCTACAGGA TTGAGACGGA GGGGGAGAAG
CAGGAGCTGT GGAAATATAC GATCGACAAT GTTTCCCCCC ACGCACAGCC GGAGGAGGAG
GAGCGGGAAC GGCGAGTGTT CAAGGATCTT TATGGCCGGC ACAAGGAGTA TCTCAGCAGC
CTCGTAGGCA CCGACTTTGA GATGACTGTC CCAGGTGCCC TCCGGCTCTT TGTAAATGGA
GAGGTCGTTT CAGCCCAAGG CTATGAGTAT GACAATCTCT ACGTCCACTT CTTTGTAGAA
TTGCCAACTG CTCACTGGTC AAGCCCAGCA TTCCAGCAGC TCTCAGGAGT AACACAGACC
TGCACCACCA AGTCCCTGGC AATGGACAAG GTGGCTCACT TCTCCTACCC ATTCACGTTT
GAAGCCTTCT TCCTCCATGA GGATGAATCT TCTGATGCAC TCCCGGAGTG GCCTGTGCTC
TACTGTGAGG TCCTCTCGCT GGACTTCTGG CAGAGGTACC GTGTGGAAGG CTATGGGGCT
GTGGTGCTGC CTGCCACTCC AGGCTCACAC ACCCTGACAG TCTCCACGTG GAGACCTGTG
GAGCTTGGCA CGGTGGCTGA GCTGAGGAGG TTTTTCATTG GCGGTTCTCT GGAACTGGAG
GACCTCTCCT ATGTACGGAT ACCAGGATCC TTCAAGGGCC TTCATGGAAT CGAGCTCCCT
TCAGAAAAGG ATGCGGAGTG TGTTGGACCG TCTGGAAGGG TTCAGCCAGC AGAGTTCCAT
TCACAATGTG CTAGAGGCCT TCCGTCGAGC CCGGCGCCGC ATGCAGGAGG CCCGGGAAAG
CCTCCCGCAG GACCTAGTGA GCCCCTCTGG AACCCTGGTC TCCTAGCTCA CAGCAGCCCT
GGCCCACAGT GCAAGAGGAC AAGATGGGGG ATATCTGAGG CCAGTGCTCT CCTGCCTCTT
CGTCTTTCTG ATTAG

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

CloneID OHu68759
Clone ID Related Accession (Same CDS sequence) XM_011524958
Accession Version XM_011524958.1 Documents for ORF clone product in dufault vector
Sequence Information ORF Nucleotide Sequence (Length: 1689bp)
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
ORF Insert Method CloneEZ® Seamless cloning technology
Structure linear
Update Date 12-MAR-2015
Organism Homo sapiens (human)
Product Meckel syndrome type 1 protein isoform X2
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
1081
1141
1201
1261
1321
1381
1441
1501
1561
1621
1681
ATGGCGGAGA CCGTCTGGAG CACTGACACC GGGGAGGCAG TGTATCGCTC CCGGGACCCC 
GTGCGCAACT TGCGCCTCCG AGTCCACCTG CAAAGAATCA CATCAAGCAA CTTTCTTCAT
TATCAGCCTG CTGCCGAGCT CGGGAAGGAC CTCATAGACT TGGCCACTTT TAGGCCTCAG
CCAACTGCCA TCTTTGGAGG TGGACACCGC CCAGAGGAAG ACGAAGAGGA GGAGATTGTG
ATTGGGTGGC AGGAGAAGCT CTTTAGCCAG TTTGAAGTAG ATCTGTACCA AAATGAAACA
GCCTGTCAGA GTCCTTTGGA TTATCAGTAC CGTCAGGAGA TCCTGAAGCT GGAGAATTCG
GGTGGCAAGA AAAACCGACG AATCTTTACC TACACTGACT CTGATAGATA CACCAATTTG
GAGGAGCACT GTCAGAGAAT GACCACTGCA GCCAGCGAGG TGCCTTCATT CTTGGTCGAG
CGAATGGCAA ATGTCAGGCG TCGCCGGCAG GACAGGCGAG GGATGGAGGG CGGCATCCTC
AAGTCACGCA TCGTCACCTG GGAGCCCTCA GAAGAGTTTG TCAGGAACAA CCACGTCATT
AACACCCCTC TTCAGACAAT GCACATCATG GCAGACCTGG GGCCCTATAA AAAGCTTGGC
TATAAGAAGT ATGAACATGT CCTGTGTACT CTGAAGGTGG ATAGCAATGG TGTGATCACA
GTAAAGCCTG ACTTCACGGG CCTCAAAGGA CCCTACAGGA TTGAGACGGA GGGGGAGAAG
CAGGAGCTGT GGAAATATAC GATCGACAAT GTTTCCCCCC ACGCACAGCC GGAGGAGGAG
GAGCGGGAAC GGCGAGTGTT CAAGGATCTT TATGGCCGGC ACAAGGAGTA TCTCAGCAGC
CTCGTAGGCA CCGACTTTGA GATGACTGTC CCAGGTGCCC TCCGGCTCTT TGTAAATGGA
GAGGTCGTTT CAGCCCAAGG CTATGAGTAT GACAATCTCT ACGTCCACTT CTTTGTAGAA
TTGCCAACTG CTCACTGGTC AAGCCCAGCA TTCCAGCAGC TCTCAGGAGT AACACAGACC
TGCACCACCA AGTCCCTGGC AATGGACAAG GTGGCTCACT TCTCCTACCC ATTCACGTTT
GAAGCCTTCT TCCTCCATGA GGATGAATCT TCTGATGCAC TCCCGGAGTG GCCTGTGCTC
TACTGTGAGG TCCTCTCGCT GGACTTCTGG CAGAGGTACC GTGTGGAAGG CTATGGGGCT
GTGGTGCTGC CTGCCACTCC AGGCTCACAC ACCCTGACAG TCTCCACGTG GAGACCTGTG
GAGCTTGGCA CGGTGGCTGA GCTGAGGAGG TTTTTCATTG GCGGTTCTCT GGAACTGGAG
GACCTCTCCT ATGTACGGAT ACCAGGATCC TTCAAGGGGG AACGCCTGAG CCGCTTTGGA
CTCCGCACAG AGACCACAGG CACTGTCACC TTCCGCTTGC ACTGTCTGCA GCAGTCCAGG
GCCTTCATGG AATCGAGCTC CCTTCAGAAA AGGATGCGGA GTGTGTTGGA CCGTCTGGAA
GGGTTCAGCC AGCAGAGTTC CATTCACAAT GTGCTAGAGG CCTTCCGTCG AGCCCGGCGC
CGCATGCAGG AGGCCCGGGA AAGCCTCCCG CAGGACCTAG TGAGCCCCTC TGGAACCCTG
GTCTCCTAG

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

RefSeq XP_011523260.1
CDS49..1737
Misc Feature(1)991..1539(+)
Translation

Target ORF information:

RefSeq Version XM_011524958
Organism Homo sapiens (human)
Definition PREDICTED: Homo sapiens Meckel syndrome, type 1 (MKS1), transcript variant X2, mRNA.

Target ORF information:

Epitope DYKDDDDK
Bacterial selection AMPR
Mammalian selection NeoR
Vector pcDNA3.1+/C-(K)DYK
XM_011524958

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
1501
1561
1621
1681
ATGGCGGAGA CCGTCTGGAG CACTGACACC GGGGAGGCAG TGTATCGCTC CCGGGACCCC 
GTGCGCAACT TGCGCCTCCG AGTCCACCTG CAAAGAATCA CATCAAGCAA CTTTCTTCAT
TATCAGCCTG CTGCCGAGCT CGGGAAGGAC CTCATAGACT TGGCCACTTT TAGGCCTCAG
CCAACTGCCA TCTTTGGAGG TGGACACCGC CCAGAGGAAG ACGAAGAGGA GGAGATTGTG
ATTGGGTGGC AGGAGAAGCT CTTTAGCCAG TTTGAAGTAG ATCTGTACCA AAATGAAACA
GCCTGTCAGA GTCCTTTGGA TTATCAGTAC CGTCAGGAGA TCCTGAAGCT GGAGAATTCG
GGTGGCAAGA AAAACCGACG AATCTTTACC TACACTGACT CTGATAGATA CACCAATTTG
GAGGAGCACT GTCAGAGAAT GACCACTGCA GCCAGCGAGG TGCCTTCATT CTTGGTCGAG
CGAATGGCAA ATGTCAGGCG TCGCCGGCAG GACAGGCGAG GGATGGAGGG CGGCATCCTC
AAGTCACGCA TCGTCACCTG GGAGCCCTCA GAAGAGTTTG TCAGGAACAA CCACGTCATT
AACACCCCTC TTCAGACAAT GCACATCATG GCAGACCTGG GGCCCTATAA AAAGCTTGGC
TATAAGAAGT ATGAACATGT CCTGTGTACT CTGAAGGTGG ATAGCAATGG TGTGATCACA
GTAAAGCCTG ACTTCACGGG CCTCAAAGGA CCCTACAGGA TTGAGACGGA GGGGGAGAAG
CAGGAGCTGT GGAAATATAC GATCGACAAT GTTTCCCCCC ACGCACAGCC GGAGGAGGAG
GAGCGGGAAC GGCGAGTGTT CAAGGATCTT TATGGCCGGC ACAAGGAGTA TCTCAGCAGC
CTCGTAGGCA CCGACTTTGA GATGACTGTC CCAGGTGCCC TCCGGCTCTT TGTAAATGGA
GAGGTCGTTT CAGCCCAAGG CTATGAGTAT GACAATCTCT ACGTCCACTT CTTTGTAGAA
TTGCCAACTG CTCACTGGTC AAGCCCAGCA TTCCAGCAGC TCTCAGGAGT AACACAGACC
TGCACCACCA AGTCCCTGGC AATGGACAAG GTGGCTCACT TCTCCTACCC ATTCACGTTT
GAAGCCTTCT TCCTCCATGA GGATGAATCT TCTGATGCAC TCCCGGAGTG GCCTGTGCTC
TACTGTGAGG TCCTCTCGCT GGACTTCTGG CAGAGGTACC GTGTGGAAGG CTATGGGGCT
GTGGTGCTGC CTGCCACTCC AGGCTCACAC ACCCTGACAG TCTCCACGTG GAGACCTGTG
GAGCTTGGCA CGGTGGCTGA GCTGAGGAGG TTTTTCATTG GCGGTTCTCT GGAACTGGAG
GACCTCTCCT ATGTACGGAT ACCAGGATCC TTCAAGGGGG AACGCCTGAG CCGCTTTGGA
CTCCGCACAG AGACCACAGG CACTGTCACC TTCCGCTTGC ACTGTCTGCA GCAGTCCAGG
GCCTTCATGG AATCGAGCTC CCTTCAGAAA AGGATGCGGA GTGTGTTGGA CCGTCTGGAA
GGGTTCAGCC AGCAGAGTTC CATTCACAAT GTGCTAGAGG CCTTCCGTCG AGCCCGGCGC
CGCATGCAGG AGGCCCGGGA AAGCCTCCCG CAGGACCTAG TGAGCCCCTC TGGAACCCTG
GTCTCCTAG

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

CloneID OHu50503
Clone ID Related Accession (Same CDS sequence) XM_005257483
Accession Version XM_005257483.3 Documents for ORF clone product in dufault vector
Sequence Information ORF Nucleotide Sequence (Length: 1686bp)
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
ORF Insert Method CloneEZ® Seamless cloning technology
Structure linear
Update Date 12-MAR-2015
Organism Homo sapiens (human)
Product Meckel syndrome type 1 protein isoform X3
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 On Mar 12, 2015 this sequence version replaced gi:578831107. ##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
1501
1561
1621
1681
ATGGCGGAGA CCGTCTGGAG CACTGACACC GGGGAGGCAG TGTATCGCTC CCGGGACCCC 
GTGCGCAACT TGCGCCTCCG AGTCCACCTG CAAAGAATCA CATCAAGCAA CTTTCTTCAT
TATCAGCCTG CTGCCGAGCT CGGGAAGGAC CTCATAGACT TGGCCACTTT TAGGCCTCAG
CCAACTGCCA GTGGACACCG CCCAGAGGAA GACGAAGAGG AGGAGATTGT GATTGGGTGG
CAGGAGAAGC TCTTTAGCCA GTTTGAAGTA GATCTGTACC AAAATGAAAC AGCCTGTCAG
AGTCCTTTGG ATTATCAGTA CCGTCAGGAG ATCCTGAAGC TGGAGAATTC GGGTGGCAAG
AAAAACCGAC GAATCTTTAC CTACACTGAC TCTGATAGAT ACACCAATTT GGAGGAGCAC
TGTCAGAGAA TGACCACTGC AGCCAGCGAG GTGCCTTCAT TCTTGGTCGA GCGAATGGCA
AATGTCAGGC GTCGCCGGCA GGACAGGCGA GGGATGGAGG GCGGCATCCT CAAGTCACGC
ATCGTCACCT GGGAGCCCTC AGAAGAGTTT GTCAGGAACA ACCACGTCAT TAACACCCCT
CTTCAGACAA TGCACATCAT GGCAGACCTG GGGCCCTATA AAAAGCTTGG CTATAAGAAG
TATGAACATG TCCTGTGTAC TCTGAAGGTG GATAGCAATG GTGTGATCAC AGTAAAGCCT
GACTTCACGG GCCTCAAAGG ACCCTACAGG ATTGAGACGG AGGGGGAGAA GCAGGAGCTG
TGGAAATATA CGATCGACAA TGTTTCCCCC CACGCACAGC CGGAGGAGGA GGAGCGGGAA
CGGCGAGTGT TCAAGGATCT TTATGGCCGG CACAAGGAGT ATCTCAGCAG CCTCGTAGGC
ACCGACTTTG AGATGACTGT CCCAGGTGCC CTCCGGCTCT TTGTAAATGG AGAGGTCGTT
TCAGCCCAAG GCTATGAGTA TGACAATCTC TACGTCCACT TCTTTGTAGA ATTGCCAACT
GCTCACTGGT CAAGCCCAGC ATTCCAGCAG CTCTCAGGAG TAACACAGAC CTGCACCACC
AAGTCCCTGG CAATGGACAA GGTGGCTCAC TTCTCCTACC CATTCACGTT TGAAGCCTTC
TTCCTCCATG AGGATGAATC TTCTGATGCA CTCCCGGAGT GGCCTGTGCT CTACTGTGAG
GTCCTCTCGC TGGACTTCTG GCAGAGGTAC CGTGTGGAAG GCTATGGGGC TGTGGTGCTG
CCTGCCACTC CAGGCTCACA CACCCTGACA GTCTCCACGT GGAGACCTGT GGAGCTTGGC
ACGGTGGCTG AGCTGAGGAG GTTTTTCATT GGCGGTTCTC TGGAACTGGA GGACCTCTCC
TATGTACGGA TACCAGGATC CTTCAAGGGC CTTCATGGAA TCGAGCTCCC TTCAGAAAAG
GATGCGGAGT GTGTTGGACC GTCTGGAAGG GTTCAGCCAG CAGAGTTCCA TTCACAATGT
GCTAGAGGCC TTCCGTCGAG CCCGGCGCCG CATGCAGGAG GCCCGGGAAA GCCTCCCGCA
GGACCTAGTG AGCCCCTCTG GAACCCTGGT CTCCTAGCTC ACAGCAGCCC TGGCCCACAG
TGCAAGAGGA CAAGATGGGG GATATCTGAG GCCAGTGCTC TCCTGCCTCT TCGTCTTTCT
GATTAG

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

RefSeq XP_005257540.1
CDS62..1747
Misc Feature(1)995..1477(+)
Translation

Target ORF information:

RefSeq Version XM_005257483
Organism Homo sapiens (human)
Definition PREDICTED: Homo sapiens Meckel syndrome, type 1 (MKS1), transcript variant X3, mRNA.

Target ORF information:

Epitope DYKDDDDK
Bacterial selection AMPR
Mammalian selection NeoR
Vector pcDNA3.1+/C-(K)DYK
XM_005257483

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
1501
1561
1621
1681
ATGGCGGAGA CCGTCTGGAG CACTGACACC GGGGAGGCAG TGTATCGCTC CCGGGACCCC 
GTGCGCAACT TGCGCCTCCG AGTCCACCTG CAAAGAATCA CATCAAGCAA CTTTCTTCAT
TATCAGCCTG CTGCCGAGCT CGGGAAGGAC CTCATAGACT TGGCCACTTT TAGGCCTCAG
CCAACTGCCA GTGGACACCG CCCAGAGGAA GACGAAGAGG AGGAGATTGT GATTGGGTGG
CAGGAGAAGC TCTTTAGCCA GTTTGAAGTA GATCTGTACC AAAATGAAAC AGCCTGTCAG
AGTCCTTTGG ATTATCAGTA CCGTCAGGAG ATCCTGAAGC TGGAGAATTC GGGTGGCAAG
AAAAACCGAC GAATCTTTAC CTACACTGAC TCTGATAGAT ACACCAATTT GGAGGAGCAC
TGTCAGAGAA TGACCACTGC AGCCAGCGAG GTGCCTTCAT TCTTGGTCGA GCGAATGGCA
AATGTCAGGC GTCGCCGGCA GGACAGGCGA GGGATGGAGG GCGGCATCCT CAAGTCACGC
ATCGTCACCT GGGAGCCCTC AGAAGAGTTT GTCAGGAACA ACCACGTCAT TAACACCCCT
CTTCAGACAA TGCACATCAT GGCAGACCTG GGGCCCTATA AAAAGCTTGG CTATAAGAAG
TATGAACATG TCCTGTGTAC TCTGAAGGTG GATAGCAATG GTGTGATCAC AGTAAAGCCT
GACTTCACGG GCCTCAAAGG ACCCTACAGG ATTGAGACGG AGGGGGAGAA GCAGGAGCTG
TGGAAATATA CGATCGACAA TGTTTCCCCC CACGCACAGC CGGAGGAGGA GGAGCGGGAA
CGGCGAGTGT TCAAGGATCT TTATGGCCGG CACAAGGAGT ATCTCAGCAG CCTCGTAGGC
ACCGACTTTG AGATGACTGT CCCAGGTGCC CTCCGGCTCT TTGTAAATGG AGAGGTCGTT
TCAGCCCAAG GCTATGAGTA TGACAATCTC TACGTCCACT TCTTTGTAGA ATTGCCAACT
GCTCACTGGT CAAGCCCAGC ATTCCAGCAG CTCTCAGGAG TAACACAGAC CTGCACCACC
AAGTCCCTGG CAATGGACAA GGTGGCTCAC TTCTCCTACC CATTCACGTT TGAAGCCTTC
TTCCTCCATG AGGATGAATC TTCTGATGCA CTCCCGGAGT GGCCTGTGCT CTACTGTGAG
GTCCTCTCGC TGGACTTCTG GCAGAGGTAC CGTGTGGAAG GCTATGGGGC TGTGGTGCTG
CCTGCCACTC CAGGCTCACA CACCCTGACA GTCTCCACGT GGAGACCTGT GGAGCTTGGC
ACGGTGGCTG AGCTGAGGAG GTTTTTCATT GGCGGTTCTC TGGAACTGGA GGACCTCTCC
TATGTACGGA TACCAGGATC CTTCAAGGGC CTTCATGGAA TCGAGCTCCC TTCAGAAAAG
GATGCGGAGT GTGTTGGACC GTCTGGAAGG GTTCAGCCAG CAGAGTTCCA TTCACAATGT
GCTAGAGGCC TTCCGTCGAG CCCGGCGCCG CATGCAGGAG GCCCGGGAAA GCCTCCCGCA
GGACCTAGTG AGCCCCTCTG GAACCCTGGT CTCCTAGCTC ACAGCAGCCC TGGCCCACAG
TGCAAGAGGA CAAGATGGGG GATATCTGAG GCCAGTGCTC TCCTGCCTCT TCGTCTTTCT
GATTAG

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

CloneID OHu68760
Clone ID Related Accession (Same CDS sequence) XM_011524959
Accession Version XM_011524959.1 Documents for ORF clone product in dufault vector
Sequence Information ORF Nucleotide Sequence (Length: 1380bp)
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
ORF Insert Method CloneEZ® Seamless cloning technology
Structure linear
Update Date 12-MAR-2015
Organism Homo sapiens (human)
Product Meckel syndrome type 1 protein isoform X4
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 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
1081
1141
1201
1261
1321
ATGGCGGAGA CCGTCTGGAG CACTGACACC GGGGAGGCAG TGTATCGCTC CCGGGACCCC 
GTGCGCAACT TGCGCCTCCG AGTCCACCTG CAAAGAATCA CATCAAGCAA CTTTCTTCAT
TATCAGCCTG CTGCCGAGCT CGGGAAGGAC CTCATAGACT TGGCCACTTT TAGGCCTCAG
CCAACTGCCA TCTTTGGAGG TGGACACCGC CCAGAGGAAG ACGAAGAGGA GGAGATTGTG
ATTGGGTGGC AGGAGAAGCT CTTTAGCCAG TTTGAAGTAG ATCTGTACCA AAATGAAACA
GCCTGTCAGA GTCCTTTGGA TTATCAGTAC CGTCAGGAGA TCCTGAAGCT GGAGAATTCG
GGTGGCAAGA AAAACCGACG AATCTTTACC TACACTGACT CTGATAGATA CACCAATTTG
GAGGAGCACT GTCAGAGAAT GACCACTGCA GCCAGCGAGG TGCCTTCATT CTTGGTCGAG
CGAATGGCAA ATGTCAGGCG TCGCCGGCAG GACAGGCGAG GGATGGAGGG CGGCATCCTC
AAGTCACGCA TCGTCACCTG GGAGCCCTCA GAAGAGTTTG TCAGGAACAA CCACGTCATT
AACACCCCTC TTCAGACAAT GCACATCATG GCAGACCTGG GGCCCTATAA AAAGCTTGGC
TATAAGAAGT ATGAACATGT CCTGTGTACT CTGAAGGTGG ATAGCAATGG TGTGATCACA
GTAAAGCCTG ACTTCACGGG CCTCAAAGGA CCCTACAGGA TTGAGACGGA GGGGGAGAAG
CAGGAGCTGT GGAAATATAC GATCGACAAT GTTTCCCCCC ACGCACAGCC GGAGGAGGAG
GAGCGGGAAC GGCGAGTGTT CAAGGATCTT TATGGCCGGC ACAAGGAGTA TCTCAGCAGC
CTCGTAGGCA CCGACTTTGA GATGACTGTC CCAGGTGCCC TCCGGCTCTT TGTAAATGGA
GAGGTCGTTT CAGCCCAAGG CTATGAGTAT GACAATCTCT ACGTCCACTT CTTTGTAGAA
TTGCCAACTG CTCACTGGTC AAGCCCAGCA TTCCAGCAGC TCTCAGGAGT AACACAGACC
TGCACCACCA AGTCCCTGGC AATGGACAAG GTGGCTCACT TCTCCTACCC ATTCACGTTT
GAAGCCTTCT TCCTCCATGA GGATGAATCT TCTGATGCAC TCCCGGAGTG GCCTGTGCTC
TACTGTGAGG TCCTCTCGCT GGACTTCTGG CAGAGGTACC GTGTGGAAGG CTATGGGGCT
GTGGTGCTGC CTGCCACTCC AGGGCCTTCA TGGAATCGAG CTCCCTTCAG AAAAGGATGC
GGAGTGTGTT GGACCGTCTG GAAGGGTTCA GCCAGCAGAG TTCCATTCAC AATGTGCTAG

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

RefSeq XP_011523261.1
CDS49..1428
Misc Feature(1)991..>1332(+)
Translation

Target ORF information:

RefSeq Version XM_011524959
Organism Homo sapiens (human)
Definition PREDICTED: Homo sapiens Meckel syndrome, type 1 (MKS1), transcript variant X4, mRNA.

Target ORF information:

Epitope DYKDDDDK
Bacterial selection AMPR
Mammalian selection NeoR
Vector pcDNA3.1+/C-(K)DYK
XM_011524959

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
ATGGCGGAGA CCGTCTGGAG CACTGACACC GGGGAGGCAG TGTATCGCTC CCGGGACCCC 
GTGCGCAACT TGCGCCTCCG AGTCCACCTG CAAAGAATCA CATCAAGCAA CTTTCTTCAT
TATCAGCCTG CTGCCGAGCT CGGGAAGGAC CTCATAGACT TGGCCACTTT TAGGCCTCAG
CCAACTGCCA TCTTTGGAGG TGGACACCGC CCAGAGGAAG ACGAAGAGGA GGAGATTGTG
ATTGGGTGGC AGGAGAAGCT CTTTAGCCAG TTTGAAGTAG ATCTGTACCA AAATGAAACA
GCCTGTCAGA GTCCTTTGGA TTATCAGTAC CGTCAGGAGA TCCTGAAGCT GGAGAATTCG
GGTGGCAAGA AAAACCGACG AATCTTTACC TACACTGACT CTGATAGATA CACCAATTTG
GAGGAGCACT GTCAGAGAAT GACCACTGCA GCCAGCGAGG TGCCTTCATT CTTGGTCGAG
CGAATGGCAA ATGTCAGGCG TCGCCGGCAG GACAGGCGAG GGATGGAGGG CGGCATCCTC
AAGTCACGCA TCGTCACCTG GGAGCCCTCA GAAGAGTTTG TCAGGAACAA CCACGTCATT
AACACCCCTC TTCAGACAAT GCACATCATG GCAGACCTGG GGCCCTATAA AAAGCTTGGC
TATAAGAAGT ATGAACATGT CCTGTGTACT CTGAAGGTGG ATAGCAATGG TGTGATCACA
GTAAAGCCTG ACTTCACGGG CCTCAAAGGA CCCTACAGGA TTGAGACGGA GGGGGAGAAG
CAGGAGCTGT GGAAATATAC GATCGACAAT GTTTCCCCCC ACGCACAGCC GGAGGAGGAG
GAGCGGGAAC GGCGAGTGTT CAAGGATCTT TATGGCCGGC ACAAGGAGTA TCTCAGCAGC
CTCGTAGGCA CCGACTTTGA GATGACTGTC CCAGGTGCCC TCCGGCTCTT TGTAAATGGA
GAGGTCGTTT CAGCCCAAGG CTATGAGTAT GACAATCTCT ACGTCCACTT CTTTGTAGAA
TTGCCAACTG CTCACTGGTC AAGCCCAGCA TTCCAGCAGC TCTCAGGAGT AACACAGACC
TGCACCACCA AGTCCCTGGC AATGGACAAG GTGGCTCACT TCTCCTACCC ATTCACGTTT
GAAGCCTTCT TCCTCCATGA GGATGAATCT TCTGATGCAC TCCCGGAGTG GCCTGTGCTC
TACTGTGAGG TCCTCTCGCT GGACTTCTGG CAGAGGTACC GTGTGGAAGG CTATGGGGCT
GTGGTGCTGC CTGCCACTCC AGGGCCTTCA TGGAATCGAG CTCCCTTCAG AAAAGGATGC
GGAGTGTGTT GGACCGTCTG GAAGGGTTCA GCCAGCAGAG TTCCATTCAC AATGTGCTAG

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

CloneID OHu68761
Clone ID Related Accession (Same CDS sequence) XM_011524960
Accession Version XM_011524960.1 Documents for ORF clone product in dufault vector
Sequence Information ORF Nucleotide Sequence (Length: 1308bp)
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
ORF Insert Method CloneEZ® Seamless cloning technology
Structure linear
Update Date 12-MAR-2015
Organism Homo sapiens (human)
Product Meckel syndrome type 1 protein isoform X5
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 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
1081
1141
1201
1261
ATGGCGGAGA CCGTCTGGAG CACTGACACC GGGGAGGCAG TGTATCGCTC CCGGGACCCC 
GTGCGCAACT TGCGCCTCCG AGTCCACCTG CAAAGAATCA CATCAAGCAA CTTTCTTCAT
TATCAGCCTG CTGCCGAGCT CGGGAAGGAC CTCATAGACT TGGCCACTTT TAGGCCTCAG
CCAACTGCCA TCTTTGGAGG TGGACACCGC CCAGAGGAAG ACGAAGAGGA GGAGATTGTG
ATTGGGTGGC AGGAGAAGCT CTTTAGCCAG TTTGAAGTAG ATCTGTACCA AAATGAAACA
GCCTGTCAGA GTCCTTTGGA TTATCAGTAC CGTCAGGAGA TCCTGAAGCT GGAGAATTCG
GGTGGCAAGA AAAACCGACG AATCTTTACC TACACTGACT CTGATAGATA CACCAATTTG
GAGGAGCACT GTCAGAGAAT GACCACTGCA GCCAGCGAGG TGCCTTCATT CTTGGTCGAG
CGAATGGCAA ATGTCAGGCG TCGCCGGCAG GACAGGCGAG GGATGGAGGG CGGCATCCTC
AAGTCACGCA TCGTCACCTG GGAGCCCTCA GAAGAGTTTG TCAGGAACAA CCACGTCATT
AACACCCCTC TTCAGACAAT GCACATCATG GCAGACCTGG GGCCCTATAA AAAGCTTGGC
TATAAGAAGT ATGAACATGT CCTGTGTACT CTGAAGGTGG ATAGCAATGG TGTGATCACA
GTAAAGCCTG ACTTCACGGG CCTCAAAGGA CCCTACAGGA TTGAGACGGA GGGGGAGAAG
CAGGAGCTGT GGAAATATAC GATCGACAAT GTTTCCCCCC ACGCACAGCC GGAGGAGGAG
GAGCGGGAAC GGCGAGTGTT CAAGGATCTT TATGGCCGGC ACAAGGAGTA TCTCAGCAGC
CTCGTAGGCA CCGACTTTGA GATGACTGTC CCAGGTGCCC TCCGGCTCTT TGTAAATGGA
GAGGTCGTTT CAGCCCAAGG CTATGAGTAT GACAATCTCT ACGTCCACTT CTTTGTAGAA
TTGCCAACTG CTCACTGGTC AAGCCCAGCA TTCCAGCAGC TCTCAGGAGT AACACAGACC
TGCACCACCA AGTCCCTGGC AATGGACAAG GTGGCTCACT TCTCCTACCC ATTCACGTTT
GAAGCCTTCT TCCTCCATGA GGATGAATCT TCTGATGCAC TCCCGGAGTG GCCTGTGCTC
TACTGTGAGG TCCTCTCGCT GGACTTCTGG CAGAGGTACC GTGTGGAAGG CTATGGGGCT
GTGGTGCTGC CTGCCACTCC AGCGACAATG ACGTGGCCTT GGCACTGA

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

RefSeq XP_011523262.1
CDS49..1356
Misc Feature(1)991..>1329(+)
Translation

Target ORF information:

RefSeq Version XM_011524960
Organism Homo sapiens (human)
Definition PREDICTED: Homo sapiens Meckel syndrome, type 1 (MKS1), transcript variant X5, mRNA.

Target ORF information:

Epitope DYKDDDDK
Bacterial selection AMPR
Mammalian selection NeoR
Vector pcDNA3.1+/C-(K)DYK
XM_011524960

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
ATGGCGGAGA CCGTCTGGAG CACTGACACC GGGGAGGCAG TGTATCGCTC CCGGGACCCC 
GTGCGCAACT TGCGCCTCCG AGTCCACCTG CAAAGAATCA CATCAAGCAA CTTTCTTCAT
TATCAGCCTG CTGCCGAGCT CGGGAAGGAC CTCATAGACT TGGCCACTTT TAGGCCTCAG
CCAACTGCCA TCTTTGGAGG TGGACACCGC CCAGAGGAAG ACGAAGAGGA GGAGATTGTG
ATTGGGTGGC AGGAGAAGCT CTTTAGCCAG TTTGAAGTAG ATCTGTACCA AAATGAAACA
GCCTGTCAGA GTCCTTTGGA TTATCAGTAC CGTCAGGAGA TCCTGAAGCT GGAGAATTCG
GGTGGCAAGA AAAACCGACG AATCTTTACC TACACTGACT CTGATAGATA CACCAATTTG
GAGGAGCACT GTCAGAGAAT GACCACTGCA GCCAGCGAGG TGCCTTCATT CTTGGTCGAG
CGAATGGCAA ATGTCAGGCG TCGCCGGCAG GACAGGCGAG GGATGGAGGG CGGCATCCTC
AAGTCACGCA TCGTCACCTG GGAGCCCTCA GAAGAGTTTG TCAGGAACAA CCACGTCATT
AACACCCCTC TTCAGACAAT GCACATCATG GCAGACCTGG GGCCCTATAA AAAGCTTGGC
TATAAGAAGT ATGAACATGT CCTGTGTACT CTGAAGGTGG ATAGCAATGG TGTGATCACA
GTAAAGCCTG ACTTCACGGG CCTCAAAGGA CCCTACAGGA TTGAGACGGA GGGGGAGAAG
CAGGAGCTGT GGAAATATAC GATCGACAAT GTTTCCCCCC ACGCACAGCC GGAGGAGGAG
GAGCGGGAAC GGCGAGTGTT CAAGGATCTT TATGGCCGGC ACAAGGAGTA TCTCAGCAGC
CTCGTAGGCA CCGACTTTGA GATGACTGTC CCAGGTGCCC TCCGGCTCTT TGTAAATGGA
GAGGTCGTTT CAGCCCAAGG CTATGAGTAT GACAATCTCT ACGTCCACTT CTTTGTAGAA
TTGCCAACTG CTCACTGGTC AAGCCCAGCA TTCCAGCAGC TCTCAGGAGT AACACAGACC
TGCACCACCA AGTCCCTGGC AATGGACAAG GTGGCTCACT TCTCCTACCC ATTCACGTTT
GAAGCCTTCT TCCTCCATGA GGATGAATCT TCTGATGCAC TCCCGGAGTG GCCTGTGCTC
TACTGTGAGG TCCTCTCGCT GGACTTCTGG CAGAGGTACC GTGTGGAAGG CTATGGGGCT
GTGGTGCTGC CTGCCACTCC AGCGACAATG ACGTGGCCTT GGCACTGA

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

CloneID OHu50506
Clone ID Related Accession (Same CDS sequence) XM_005257485
Accession Version XM_005257485.3 Documents for ORF clone product in dufault vector
Sequence Information ORF Nucleotide Sequence (Length: 1257bp)
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
ORF Insert Method CloneEZ® Seamless cloning technology
Structure linear
Update Date 12-MAR-2015
Organism Homo sapiens (human)
Product Meckel syndrome type 1 protein isoform X6
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 EST evidence. Also see: Documentation of NCBI's Annotation Process On Mar 12, 2015 this sequence version replaced gi:578831111. ##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
ATGACCACTG CAGCCAGCGA GGTGCCTTCA TTCTTGGTCG AGCGAATGGC AAATGTCAGG 
CGTCGCCGGC AGGACAGGCG AGGGATGGAG GGCGGCATCC TCAAGTCACG CATCGTCACC
TGGGAGCCCT CAGAAGAGTT TGTCAGGAAC AACCACGTCA TTAACACCCC TCTTCAGACA
ATGCACATCA TGGCAGACCT GGGGCCCTAT AAAAAGCTTG GCTATAAGAA GTATGAACAT
GTCCTGTGTA CTCTGAAGGT GGATAGCAAT GGTGTGATCA CAGTAAAGCC TGACTTCACG
GGCCTCAAAG GACCCTACAG GATTGAGACG GAGGGGGAGA AGCAGGAGCT GTGGAAATAT
ACGATCGACA ATGTTTCCCC CCACGCACAG CCGGAGGAGG AGGAGCGGGA ACGGCGAGTG
TTCAAGGATC TTTATGGCCG GCACAAGGAG TATCTCAGCA GCCTCGTAGG CACCGACTTT
GAGATGACTG TCCCAGGTGC CCTCCGGCTC TTTGTAAATG GAGAGGTCGT TTCAGCCCAA
GGCTATGAGT ATGACAATCT CTACGTCCAC TTCTTTGTAG AATTGCCAAC TGCTCACTGG
TCAAGCCCAG CATTCCAGCA GCTCTCAGGA GTAACACAGA CCTGCACCAC CAAGTCCCTG
GCAATGGACA AGGTGGCTCA CTTCTCCTAC CCATTCACGT TTGAAGCCTT CTTCCTCCAT
GAGGATGAAT CTTCTGATGC ACTCCCGGAG TGGCCTGTGC TCTACTGTGA GGTCCTCTCG
CTGGACTTCT GGCAGAGGTA CCGTGTGGAA GGCTATGGGG CTGTGGTGCT GCCTGCCACT
CCAGGCTCAC ACACCCTGAC AGTCTCCACG TGGAGACCTG TGGAGCTTGG CACGGTGGCT
GAGCTGAGGA GGTTTTTCAT TGGCGGTTCT CTGGAACTGG AGGACCTCTC CTATGTACGG
ATACCAGGAT CCTTCAAGGG CCTTCATGGA ATCGAGCTCC CTTCAGAAAA GGATGCGGAG
TGTGTTGGAC CGTCTGGAAG GGTTCAGCCA GCAGAGTTCC ATTCACAATG TGCTAGAGGC
CTTCCGTCGA GCCCGGCGCC GCATGCAGGA GGCCCGGGAA AGCCTCCCGC AGGACCTAGT
GAGCCCCTCT GGAACCCTGG TCTCCTAGCT CACAGCAGCC CTGGCCCACA GTGCAAGAGG
ACAAGATGGG GGATATCTGA GGCCAGTGCT CTCCTGCCTC TTCGTCTTTC TGATTAG

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

RefSeq XP_005257542.1
CDS486..1742
Misc Feature(1)990..1472(+)
Translation

Target ORF information:

RefSeq Version XM_005257485
Organism Homo sapiens (human)
Definition PREDICTED: Homo sapiens Meckel syndrome, type 1 (MKS1), transcript variant X6, mRNA.

Target ORF information:

Epitope DYKDDDDK
Bacterial selection AMPR
Mammalian selection NeoR
Vector pcDNA3.1+/C-(K)DYK
XM_005257485

ORF Insert Sequence:

1
61
121
181
241
301
361
421
481
541
601
661
721
781
841
901
961
1021
1081
1141
1201
ATGACCACTG CAGCCAGCGA GGTGCCTTCA TTCTTGGTCG AGCGAATGGC AAATGTCAGG 
CGTCGCCGGC AGGACAGGCG AGGGATGGAG GGCGGCATCC TCAAGTCACG CATCGTCACC
TGGGAGCCCT CAGAAGAGTT TGTCAGGAAC AACCACGTCA TTAACACCCC TCTTCAGACA
ATGCACATCA TGGCAGACCT GGGGCCCTAT AAAAAGCTTG GCTATAAGAA GTATGAACAT
GTCCTGTGTA CTCTGAAGGT GGATAGCAAT GGTGTGATCA CAGTAAAGCC TGACTTCACG
GGCCTCAAAG GACCCTACAG GATTGAGACG GAGGGGGAGA AGCAGGAGCT GTGGAAATAT
ACGATCGACA ATGTTTCCCC CCACGCACAG CCGGAGGAGG AGGAGCGGGA ACGGCGAGTG
TTCAAGGATC TTTATGGCCG GCACAAGGAG TATCTCAGCA GCCTCGTAGG CACCGACTTT
GAGATGACTG TCCCAGGTGC CCTCCGGCTC TTTGTAAATG GAGAGGTCGT TTCAGCCCAA
GGCTATGAGT ATGACAATCT CTACGTCCAC TTCTTTGTAG AATTGCCAAC TGCTCACTGG
TCAAGCCCAG CATTCCAGCA GCTCTCAGGA GTAACACAGA CCTGCACCAC CAAGTCCCTG
GCAATGGACA AGGTGGCTCA CTTCTCCTAC CCATTCACGT TTGAAGCCTT CTTCCTCCAT
GAGGATGAAT CTTCTGATGC ACTCCCGGAG TGGCCTGTGC TCTACTGTGA GGTCCTCTCG
CTGGACTTCT GGCAGAGGTA CCGTGTGGAA GGCTATGGGG CTGTGGTGCT GCCTGCCACT
CCAGGCTCAC ACACCCTGAC AGTCTCCACG TGGAGACCTG TGGAGCTTGG CACGGTGGCT
GAGCTGAGGA GGTTTTTCAT TGGCGGTTCT CTGGAACTGG AGGACCTCTC CTATGTACGG
ATACCAGGAT CCTTCAAGGG CCTTCATGGA ATCGAGCTCC CTTCAGAAAA GGATGCGGAG
TGTGTTGGAC CGTCTGGAAG GGTTCAGCCA GCAGAGTTCC ATTCACAATG TGCTAGAGGC
CTTCCGTCGA GCCCGGCGCC GCATGCAGGA GGCCCGGGAA AGCCTCCCGC AGGACCTAGT
GAGCCCCTCT GGAACCCTGG TCTCCTAGCT CACAGCAGCC CTGGCCCACA GTGCAAGAGG
ACAAGATGGG GGATATCTGA GGCCAGTGCT CTCCTGCCTC TTCGTCTTTC TGATTAG

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

CloneID OHu50507
Clone ID Related Accession (Same CDS sequence) XM_006721965
Accession Version XM_006721965.2 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
ORF Insert Method CloneEZ® Seamless cloning technology
Structure linear
Update Date 12-MAR-2015
Organism Homo sapiens (human)
Product Meckel syndrome type 1 protein isoform X7
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 EST evidence. Also see: Documentation of NCBI's Annotation Process On Mar 12, 2015 this sequence version replaced gi:578831112. ##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
ATGCACATCA TGGCAGACCT GGGGCCCTAT AAAAAGCTTG GCTATAAGAA GTATGAACAT 
GTCCTGTGTA CTCTGAAGGT GGATAGCAAT GGTGTGATCA CAGTAAAGCC TGACTTCACG
GGCCTCAAAG GACCCTACAG GATTGAGACG GAGGGGGAGA AGCAGGAGCT GTGGAAATAT
ACGATCGACA ATGTTTCCCC CCACGCACAG CCGGAGGAGG AGGAGCGGGA ACGGCGAGTG
TTCAAGGATC TTTATGGCCG GCACAAGGAG TATCTCAGCA GCCTCGTAGG CACCGACTTT
GAGATGACTG TCCCAGGTGC CCTCCGGCTC TTTGTAAATG GAGAGGTCGT TTCAGCCCAA
GGCTATGAGT ATGACAATCT CTACGTCCAC TTCTTTGTAG AATTGCCAAC TGCTCACTGG
TCAAGCCCAG CATTCCAGCA GCTCTCAGGA GTAACACAGA CCTGCACCAC CAAGTCCCTG
GCAATGGACA AGGTGGCTCA CTTCTCCTAC CCATTCACGT TTGAAGCCTT CTTCCTCCAT
GAGGATGAAT CTTCTGATGC ACTCCCGGAG TGGCCTGTGC TCTACTGTGA GGTCCTCTCG
CTGGACTTCT GGCAGAGGTA CCGTGTGGAA GGCTATGGGG CTGTGGTGCT GCCTGCCACT
CCAGGCTCAC ACACCCTGAC AGTCTCCACG TGGAGACCTG TGGAGCTTGG CACGGTGGCT
GAGCTGAGGA GGTTTTTCAT TGGCGGTTCT CTGGAACTGG AGGACCTCTC CTATGTACGG
ATACCAGGAT CCTTCAAGGG CCTTCATGGA ATCGAGCTCC CTTCAGAAAA GGATGCGGAG
TGTGTTGGAC CGTCTGGAAG GGTTCAGCCA GCAGAGTTCC ATTCACAATG TGCTAGAGGC
CTTCCGTCGA GCCCGGCGCC GCATGCAGGA GGCCCGGGAA AGCCTCCCGC AGGACCTAGT
GAGCCCCTCT GGAACCCTGG TCTCCTAGCT CACAGCAGCC CTGGCCCACA GTGCAAGAGG
ACAAGATGGG GGATATCTGA GGCCAGTGCT CTCCTGCCTC TTCGTCTTTC TGATTAG

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

RefSeq XP_006722028.1
CDS519..1595
Misc Feature(1)843..1325(+)
Translation

Target ORF information:

RefSeq Version XM_006721965
Organism Homo sapiens (human)
Definition PREDICTED: Homo sapiens Meckel syndrome, type 1 (MKS1), transcript variant X7, mRNA.

Target ORF information:

Epitope DYKDDDDK
Bacterial selection AMPR
Mammalian selection NeoR
Vector pcDNA3.1+/C-(K)DYK
XM_006721965

ORF Insert Sequence:

1
61
121
181
241
301
361
421
481
541
601
661
721
781
841
901
961
1021
ATGCACATCA TGGCAGACCT GGGGCCCTAT AAAAAGCTTG GCTATAAGAA GTATGAACAT 
GTCCTGTGTA CTCTGAAGGT GGATAGCAAT GGTGTGATCA CAGTAAAGCC TGACTTCACG
GGCCTCAAAG GACCCTACAG GATTGAGACG GAGGGGGAGA AGCAGGAGCT GTGGAAATAT
ACGATCGACA ATGTTTCCCC CCACGCACAG CCGGAGGAGG AGGAGCGGGA ACGGCGAGTG
TTCAAGGATC TTTATGGCCG GCACAAGGAG TATCTCAGCA GCCTCGTAGG CACCGACTTT
GAGATGACTG TCCCAGGTGC CCTCCGGCTC TTTGTAAATG GAGAGGTCGT TTCAGCCCAA
GGCTATGAGT ATGACAATCT CTACGTCCAC TTCTTTGTAG AATTGCCAAC TGCTCACTGG
TCAAGCCCAG CATTCCAGCA GCTCTCAGGA GTAACACAGA CCTGCACCAC CAAGTCCCTG
GCAATGGACA AGGTGGCTCA CTTCTCCTAC CCATTCACGT TTGAAGCCTT CTTCCTCCAT
GAGGATGAAT CTTCTGATGC ACTCCCGGAG TGGCCTGTGC TCTACTGTGA GGTCCTCTCG
CTGGACTTCT GGCAGAGGTA CCGTGTGGAA GGCTATGGGG CTGTGGTGCT GCCTGCCACT
CCAGGCTCAC ACACCCTGAC AGTCTCCACG TGGAGACCTG TGGAGCTTGG CACGGTGGCT
GAGCTGAGGA GGTTTTTCAT TGGCGGTTCT CTGGAACTGG AGGACCTCTC CTATGTACGG
ATACCAGGAT CCTTCAAGGG CCTTCATGGA ATCGAGCTCC CTTCAGAAAA GGATGCGGAG
TGTGTTGGAC CGTCTGGAAG GGTTCAGCCA GCAGAGTTCC ATTCACAATG TGCTAGAGGC
CTTCCGTCGA GCCCGGCGCC GCATGCAGGA GGCCCGGGAA AGCCTCCCGC AGGACCTAGT
GAGCCCCTCT GGAACCCTGG TCTCCTAGCT CACAGCAGCC CTGGCCCACA GTGCAAGAGG
ACAAGATGGG GGATATCTGA GGCCAGTGCT CTCCTGCCTC TTCGTCTTTC TGATTAG

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

CloneID OHu50508
Clone ID Related Accession (Same CDS sequence) XM_005257486
Accession Version XM_005257486.3 Documents for ORF clone product in dufault vector
Sequence Information ORF Nucleotide Sequence (Length: 1071bp)
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
ORF Insert Method CloneEZ® Seamless cloning technology
Structure linear
Update Date 12-MAR-2015
Organism Homo sapiens (human)
Product Meckel syndrome type 1 protein isoform X8
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 On Mar 12, 2015 this sequence version replaced gi:578831114. ##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
ATGCACATCA TGGCAGACCT GGGGCCCTAT AAAAAGCTTG GCTATAAGAA GTATGAACAT 
GTCCTGTGTA CTCTGAAGGT GGATAGCAAT GGTGTGATCA CAGTAAAGCC TGACTTCACG
GGCCTCAAAG GACCCTACAG GATTGAGACG GAGGGGGAGA AGCAGGAGCT GTGGAAATAT
ACGATCGACA ATGTTTCCCC CCACGCACAG CCGGAGGAGG AGGAGCGGGA ACGGCGAGTG
TTCAAGGATC TTTATGGCCG GCACAAGGAG TATCTCAGCA GCCTCGTAGG CACCGACTTT
GAGATGACTG TCCCAGGTGC CCTCCGGCTC TTTGTAAATG GAGAGGTCGT TTCAGCCCAA
GGCTATGAGT ATGACAATCT CTACGTCCAC TTCTTTGTAG AATTGCCAAC TGCTCACTGG
TCAAGCCCAG CATTCCAGCA GCTCTCAGGA GTAACACAGA CCTGCACCAC CAAGTCCCTG
GCAATGGACA AGGTGGCTCA CTTCTCCTAC CCATTCACGT TTGAAGCCTT CTTCCTCCAT
GAGGATGAAT CTTCTGATGC ACTCCCGGAG TGGCCTGTGC TCTACTGTGA GGTCCTCTCG
CTGGACTTCT GGCAGAGGTA CCGTGTGGAA GGCTATGGGG CTGTGGTGCT GCCTGCCACT
CCAGGCTCAC ACACCCTGAC AGTCTCCACG TGGAGACCTG TGGAGCTTGG CACGGTGGCT
GAGCTGAGGA GGTTTTTCAT TGGCGGTTCT CTGGAACTGG AGGACCTCTC CTATGTACGG
ATACCAGGAT CCTTCAAGGG GGAACGCCTG AGCCGCTTTG GACTCCGCAC AGAGACCACA
GGCACTGTCA CCTTCCGCTT GCACTGTCTG CAGCAGTCCA GGGCCTTCAT GGAATCGAGC
TCCCTTCAGA AAAGGATGCG GAGTGTGTTG GACCGTCTGG AAGGGTTCAG CCAGCAGAGT
TCCATTCACA ATGTGCTAGA GGCCTTCCGT CGAGCCCGGC GCCGCATGCA GGAGGCCCGG
GAAAGCCTCC CGCAGGACCT AGTGAGCCCC TCTGGAACCC TGGTCTCCTA G

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

RefSeq XP_005257543.1
CDS519..1589
Misc Feature(1)843..1391(+)
Translation

Target ORF information:

RefSeq Version XM_005257486
Organism Homo sapiens (human)
Definition PREDICTED: Homo sapiens Meckel syndrome, type 1 (MKS1), transcript variant X8, mRNA.

Target ORF information:

Epitope DYKDDDDK
Bacterial selection AMPR
Mammalian selection NeoR
Vector pcDNA3.1+/C-(K)DYK
XM_005257486

ORF Insert Sequence:

1
61
121
181
241
301
361
421
481
541
601
661
721
781
841
901
961
1021
ATGCACATCA TGGCAGACCT GGGGCCCTAT AAAAAGCTTG GCTATAAGAA GTATGAACAT 
GTCCTGTGTA CTCTGAAGGT GGATAGCAAT GGTGTGATCA CAGTAAAGCC TGACTTCACG
GGCCTCAAAG GACCCTACAG GATTGAGACG GAGGGGGAGA AGCAGGAGCT GTGGAAATAT
ACGATCGACA ATGTTTCCCC CCACGCACAG CCGGAGGAGG AGGAGCGGGA ACGGCGAGTG
TTCAAGGATC TTTATGGCCG GCACAAGGAG TATCTCAGCA GCCTCGTAGG CACCGACTTT
GAGATGACTG TCCCAGGTGC CCTCCGGCTC TTTGTAAATG GAGAGGTCGT TTCAGCCCAA
GGCTATGAGT ATGACAATCT CTACGTCCAC TTCTTTGTAG AATTGCCAAC TGCTCACTGG
TCAAGCCCAG CATTCCAGCA GCTCTCAGGA GTAACACAGA CCTGCACCAC CAAGTCCCTG
GCAATGGACA AGGTGGCTCA CTTCTCCTAC CCATTCACGT TTGAAGCCTT CTTCCTCCAT
GAGGATGAAT CTTCTGATGC ACTCCCGGAG TGGCCTGTGC TCTACTGTGA GGTCCTCTCG
CTGGACTTCT GGCAGAGGTA CCGTGTGGAA GGCTATGGGG CTGTGGTGCT GCCTGCCACT
CCAGGCTCAC ACACCCTGAC AGTCTCCACG TGGAGACCTG TGGAGCTTGG CACGGTGGCT
GAGCTGAGGA GGTTTTTCAT TGGCGGTTCT CTGGAACTGG AGGACCTCTC CTATGTACGG
ATACCAGGAT CCTTCAAGGG GGAACGCCTG AGCCGCTTTG GACTCCGCAC AGAGACCACA
GGCACTGTCA CCTTCCGCTT GCACTGTCTG CAGCAGTCCA GGGCCTTCAT GGAATCGAGC
TCCCTTCAGA AAAGGATGCG GAGTGTGTTG GACCGTCTGG AAGGGTTCAG CCAGCAGAGT
TCCATTCACA ATGTGCTAGA GGCCTTCCGT CGAGCCCGGC GCCGCATGCA GGAGGCCCGG
GAAAGCCTCC CGCAGGACCT AGTGAGCCCC TCTGGAACCC TGGTCTCCTA G

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

CloneID OHu26205
Clone ID Related Accession (Same CDS sequence) NM_017777
Accession Version NM_017777.3 Documents for ORF clone product in dufault vector
Sequence Information ORF Nucleotide Sequence (Length: 1680bp)
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 Meckel syndrome type 1 protein isoform 1
Comment REVIEWED REFSEQ: This record has been curated by NCBI staff. The reference sequence was derived from DQ185029.1, AK000352.1 and BE327525.1. This sequence is a reference standard in the RefSeqGene project. On Sep 29, 2009 this sequence version replaced gi:89242136. Transcript Variant: This variant (1) represents the longer transcript and encodes the longer isoform (1). 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 :: DQ185029.1 [ECO:0000332] RNAseq introns :: mixed/partial sample support SAMEA1965299, SAMEA1966682 [ECO:0000350] ##Evidence-Data-END## COMPLETENESS: complete on the 3' 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
1501
1561
1621
ATGGCGGAGA CCGTCTGGAG CACTGACACC GGGGAGGCAG TGTATCGCTC CCGGGACCCC 
GTGCGCAACT TGCGCCTCCG AGTCCACCTG CAAAGAATCA CATCAAGCAA CTTTCTTCAT
TATCAGCCTG CTGCCGAGCT CGGGAAGGAC CTCATAGACT TGGCCACTTT TAGGCCTCAG
CCAACTGCCA GTGGACACCG CCCAGAGGAA GACGAAGAGG AGGAGATTGT GATTGGGTGG
CAGGAGAAGC TCTTTAGCCA GTTTGAAGTA GATCTGTACC AAAATGAAAC AGCCTGTCAG
AGTCCTTTGG ATTATCAGTA CCGTCAGGAG ATCCTGAAGC TGGAGAATTC GGGTGGCAAG
AAAAACCGAC GAATCTTTAC CTACACTGAC TCTGATAGAT ACACCAATTT GGAGGAGCAC
TGTCAGAGAA TGACCACTGC AGCCAGCGAG GTGCCTTCAT TCTTGGTCGA GCGAATGGCA
AATGTCAGGC GTCGCCGGCA GGACAGGCGA GGGATGGAGG GCGGCATCCT CAAGTCACGC
ATCGTCACCT GGGAGCCCTC AGAAGAGTTT GTCAGGAACA ACCACGTCAT TAACACCCCT
CTTCAGACAA TGCACATCAT GGCAGACCTG GGGCCCTATA AAAAGCTTGG CTATAAGAAG
TATGAACATG TCCTGTGTAC TCTGAAGGTG GATAGCAATG GTGTGATCAC AGTAAAGCCT
GACTTCACGG GCCTCAAAGG ACCCTACAGG ATTGAGACGG AGGGGGAGAA GCAGGAGCTG
TGGAAATATA CGATCGACAA TGTTTCCCCC CACGCACAGC CGGAGGAGGA GGAGCGGGAA
CGGCGAGTGT TCAAGGATCT TTATGGCCGG CACAAGGAGT ATCTCAGCAG CCTCGTAGGC
ACCGACTTTG AGATGACTGT CCCAGGTGCC CTCCGGCTCT TTGTAAATGG AGAGGTCGTT
TCAGCCCAAG GCTATGAGTA TGACAATCTC TACGTCCACT TCTTTGTAGA ATTGCCAACT
GCTCACTGGT CAAGCCCAGC ATTCCAGCAG CTCTCAGGAG TAACACAGAC CTGCACCACC
AAGTCCCTGG CAATGGACAA GGTGGCTCAC TTCTCCTACC CATTCACGTT TGAAGCCTTC
TTCCTCCATG AGGATGAATC TTCTGATGCA CTCCCGGAGT GGCCTGTGCT CTACTGTGAG
GTCCTCTCGC TGGACTTCTG GCAGAGGTAC CGTGTGGAAG GCTATGGGGC TGTGGTGCTG
CCTGCCACTC CAGGCTCACA CACCCTGACA GTCTCCACGT GGAGACCTGT GGAGCTTGGC
ACGGTGGCTG AGCTGAGGAG GTTTTTCATT GGCGGTTCTC TGGAACTGGA GGACCTCTCC
TATGTACGGA TACCAGGATC CTTCAAGGGG GAACGCCTGA GCCGCTTTGG ACTCCGCACA
GAGACCACAG GCACTGTCAC CTTCCGCTTG CACTGTCTGC AGCAGTCCAG GGCCTTCATG
GAATCGAGCT CCCTTCAGAA AAGGATGCGG AGTGTGTTGG ACCGTCTGGA AGGGTTCAGC
CAGCAGAGTT CCATTCACAA TGTGCTAGAG GCCTTCCGTC GAGCCCGGCG CCGCATGCAG
GAGGCCCGGG AAAGCCTCCC GCAGGACCTA GTGAGCCCCT CTGGAACCCT GGTCTCCTAG

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

RefSeq NP_060247.2
CDS76..1755
Misc Feature(1)1009..1557(+)
Exon (1)1..155
Gene:MKS1
Gene Synonym:
Exon (2)156..265
Gene:MKS1
Gene Synonym:
Exon (3)266..336
Gene:MKS1
Gene Synonym:
Exon (4)337..492
Gene:MKS1
Gene Synonym:
Exon (5)493..590
Gene:MKS1
Gene Synonym:
Exon (6)591..719
Gene:MKS1
Gene Synonym:
Exon (7)720..824
Gene:MKS1
Gene Synonym:
Exon (8)825..933
Gene:MKS1
Gene Synonym:
Exon (9)934..990
Gene:MKS1
Gene Synonym:
Exon (10)991..1033
Gene:MKS1
Gene Synonym:
Exon (11)1034..1099
Gene:MKS1
Gene Synonym:
Exon (12)1100..1170
Gene:MKS1
Gene Synonym:
Exon (13)1171..1240
Gene:MKS1
Gene Synonym:
Exon (14)1241..1348
Gene:MKS1
Gene Synonym:
Exon (15)1349..1482
Gene:MKS1
Gene Synonym:
Exon (16)1483..1565
Gene:MKS1
Gene Synonym:
Exon (17)1566..1663
Gene:MKS1
Gene Synonym:
Exon (18)1664..2398
Gene:MKS1
Gene Synonym:
Translation

Target ORF information:

RefSeq Version NM_017777
Organism Homo sapiens (human)
Definition Homo sapiens Meckel syndrome, type 1 (MKS1), transcript variant 1, mRNA.

Target ORF information:

Epitope DYKDDDDK
Bacterial selection AMPR
Mammalian selection NeoR
Vector pcDNA3.1+/C-(K)DYK
NM_017777

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
1501
1561
1621
ATGGCGGAGA CCGTCTGGAG CACTGACACC GGGGAGGCAG TGTATCGCTC CCGGGACCCC 
GTGCGCAACT TGCGCCTCCG AGTCCACCTG CAAAGAATCA CATCAAGCAA CTTTCTTCAT
TATCAGCCTG CTGCCGAGCT CGGGAAGGAC CTCATAGACT TGGCCACTTT TAGGCCTCAG
CCAACTGCCA GTGGACACCG CCCAGAGGAA GACGAAGAGG AGGAGATTGT GATTGGGTGG
CAGGAGAAGC TCTTTAGCCA GTTTGAAGTA GATCTGTACC AAAATGAAAC AGCCTGTCAG
AGTCCTTTGG ATTATCAGTA CCGTCAGGAG ATCCTGAAGC TGGAGAATTC GGGTGGCAAG
AAAAACCGAC GAATCTTTAC CTACACTGAC TCTGATAGAT ACACCAATTT GGAGGAGCAC
TGTCAGAGAA TGACCACTGC AGCCAGCGAG GTGCCTTCAT TCTTGGTCGA GCGAATGGCA
AATGTCAGGC GTCGCCGGCA GGACAGGCGA GGGATGGAGG GCGGCATCCT CAAGTCACGC
ATCGTCACCT GGGAGCCCTC AGAAGAGTTT GTCAGGAACA ACCACGTCAT TAACACCCCT
CTTCAGACAA TGCACATCAT GGCAGACCTG GGGCCCTATA AAAAGCTTGG CTATAAGAAG
TATGAACATG TCCTGTGTAC TCTGAAGGTG GATAGCAATG GTGTGATCAC AGTAAAGCCT
GACTTCACGG GCCTCAAAGG ACCCTACAGG ATTGAGACGG AGGGGGAGAA GCAGGAGCTG
TGGAAATATA CGATCGACAA TGTTTCCCCC CACGCACAGC CGGAGGAGGA GGAGCGGGAA
CGGCGAGTGT TCAAGGATCT TTATGGCCGG CACAAGGAGT ATCTCAGCAG CCTCGTAGGC
ACCGACTTTG AGATGACTGT CCCAGGTGCC CTCCGGCTCT TTGTAAATGG AGAGGTCGTT
TCAGCCCAAG GCTATGAGTA TGACAATCTC TACGTCCACT TCTTTGTAGA ATTGCCAACT
GCTCACTGGT CAAGCCCAGC ATTCCAGCAG CTCTCAGGAG TAACACAGAC CTGCACCACC
AAGTCCCTGG CAATGGACAA GGTGGCTCAC TTCTCCTACC CATTCACGTT TGAAGCCTTC
TTCCTCCATG AGGATGAATC TTCTGATGCA CTCCCGGAGT GGCCTGTGCT CTACTGTGAG
GTCCTCTCGC TGGACTTCTG GCAGAGGTAC CGTGTGGAAG GCTATGGGGC TGTGGTGCTG
CCTGCCACTC CAGGCTCACA CACCCTGACA GTCTCCACGT GGAGACCTGT GGAGCTTGGC
ACGGTGGCTG AGCTGAGGAG GTTTTTCATT GGCGGTTCTC TGGAACTGGA GGACCTCTCC
TATGTACGGA TACCAGGATC CTTCAAGGGG GAACGCCTGA GCCGCTTTGG ACTCCGCACA
GAGACCACAG GCACTGTCAC CTTCCGCTTG CACTGTCTGC AGCAGTCCAG GGCCTTCATG
GAATCGAGCT CCCTTCAGAA AAGGATGCGG AGTGTGTTGG ACCGTCTGGA AGGGTTCAGC
CAGCAGAGTT CCATTCACAA TGTGCTAGAG GCCTTCCGTC GAGCCCGGCG CCGCATGCAG
GAGGCCCGGG AAAGCCTCCC GCAGGACCTA GTGAGCCCCT CTGGAACCCT GGTCTCCTAG

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

CloneID OHu26353
Clone ID Related Accession (Same CDS sequence) NM_001165927
Accession Version NM_001165927.1 Documents for ORF clone product in dufault vector
Sequence Information ORF Nucleotide Sequence (Length: 1650bp)
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
ORF Insert Method CloneEZ® Seamless cloning technology
Structure linear
Update Date 15-MAR-2015
Organism Homo sapiens (human)
Product Meckel syndrome type 1 protein isoform 2
Comment REVIEWED REFSEQ: This record has been curated by NCBI staff. The reference sequence was derived from AK310815.1, AK000352.1 and BE327525.1. This sequence is a reference standard in the RefSeqGene project. Transcript Variant: This variant (2) represents use of an alternate promoter and 5' UTR and uses a distinct start codon, compared to variant 1. The resulting isoform (2) has a shorter and distinct N-terminus, compared to isoform 1. 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 :: AK310815.1 [ECO:0000332] RNAseq introns :: mixed/partial sample support SAMEA1965299, SAMEA1966682 [ECO:0000350] ##Evidence-Data-END## COMPLETENESS: complete on the 3' 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
1501
1561
1621
ATGGCTGTGC CAGTTTCCTC ATTTGCACAG CGCACGAGGT CCCGCTTTCG AGTCCACCTG 
CAAAGAATCA CATCAAGCAA CTTTCTTCAT TATCAGCCTG CTGCCGAGCT CGGGAAGGAC
CTCATAGACT TGGCCACTTT TAGGCCTCAG CCAACTGCCA GTGGACACCG CCCAGAGGAA
GACGAAGAGG AGGAGATTGT GATTGGGTGG CAGGAGAAGC TCTTTAGCCA GTTTGAAGTA
GATCTGTACC AAAATGAAAC AGCCTGTCAG AGTCCTTTGG ATTATCAGTA CCGTCAGGAG
ATCCTGAAGC TGGAGAATTC GGGTGGCAAG AAAAACCGAC GAATCTTTAC CTACACTGAC
TCTGATAGAT ACACCAATTT GGAGGAGCAC TGTCAGAGAA TGACCACTGC AGCCAGCGAG
GTGCCTTCAT TCTTGGTCGA GCGAATGGCA AATGTCAGGC GTCGCCGGCA GGACAGGCGA
GGGATGGAGG GCGGCATCCT CAAGTCACGC ATCGTCACCT GGGAGCCCTC AGAAGAGTTT
GTCAGGAACA ACCACGTCAT TAACACCCCT CTTCAGACAA TGCACATCAT GGCAGACCTG
GGGCCCTATA AAAAGCTTGG CTATAAGAAG TATGAACATG TCCTGTGTAC TCTGAAGGTG
GATAGCAATG GTGTGATCAC AGTAAAGCCT GACTTCACGG GCCTCAAAGG ACCCTACAGG
ATTGAGACGG AGGGGGAGAA GCAGGAGCTG TGGAAATATA CGATCGACAA TGTTTCCCCC
CACGCACAGC CGGAGGAGGA GGAGCGGGAA CGGCGAGTGT TCAAGGATCT TTATGGCCGG
CACAAGGAGT ATCTCAGCAG CCTCGTAGGC ACCGACTTTG AGATGACTGT CCCAGGTGCC
CTCCGGCTCT TTGTAAATGG AGAGGTCGTT TCAGCCCAAG GCTATGAGTA TGACAATCTC
TACGTCCACT TCTTTGTAGA ATTGCCAACT GCTCACTGGT CAAGCCCAGC ATTCCAGCAG
CTCTCAGGAG TAACACAGAC CTGCACCACC AAGTCCCTGG CAATGGACAA GGTGGCTCAC
TTCTCCTACC CATTCACGTT TGAAGCCTTC TTCCTCCATG AGGATGAATC TTCTGATGCA
CTCCCGGAGT GGCCTGTGCT CTACTGTGAG GTCCTCTCGC TGGACTTCTG GCAGAGGTAC
CGTGTGGAAG GCTATGGGGC TGTGGTGCTG CCTGCCACTC CAGGCTCACA CACCCTGACA
GTCTCCACGT GGAGACCTGT GGAGCTTGGC ACGGTGGCTG AGCTGAGGAG GTTTTTCATT
GGCGGTTCTC TGGAACTGGA GGACCTCTCC TATGTACGGA TACCAGGATC CTTCAAGGGG
GAACGCCTGA GCCGCTTTGG ACTCCGCACA GAGACCACAG GCACTGTCAC CTTCCGCTTG
CACTGTCTGC AGCAGTCCAG GGCCTTCATG GAATCGAGCT CCCTTCAGAA AAGGATGCGG
AGTGTGTTGG ACCGTCTGGA AGGGTTCAGC CAGCAGAGTT CCATTCACAA TGTGCTAGAG
GCCTTCCGTC GAGCCCGGCG CCGCATGCAG GAGGCCCGGG AAAGCCTCCC GCAGGACCTA
GTGAGCCCCT CTGGAACCCT GGTCTCCTAG

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

RefSeq NP_001159399.1
CDS95..1744
Misc Feature(1)83..85(+)
Misc Feature(2)998..1546(+)
Exon (1)1..144
Gene:MKS1
Gene Synonym:
Exon (2)145..254
Gene:MKS1
Gene Synonym:
Exon (3)255..325
Gene:MKS1
Gene Synonym:
Exon (4)326..481
Gene:MKS1
Gene Synonym:
Exon (5)482..579
Gene:MKS1
Gene Synonym:
Exon (6)580..708
Gene:MKS1
Gene Synonym:
Exon (7)709..813
Gene:MKS1
Gene Synonym:
Exon (8)814..922
Gene:MKS1
Gene Synonym:
Exon (9)923..979
Gene:MKS1
Gene Synonym:
Exon (10)980..1022
Gene:MKS1
Gene Synonym:
Exon (11)1023..1088
Gene:MKS1
Gene Synonym:
Exon (12)1089..1159
Gene:MKS1
Gene Synonym:
Exon (13)1160..1229
Gene:MKS1
Gene Synonym:
Exon (14)1230..1337
Gene:MKS1
Gene Synonym:
Exon (15)1338..1471
Gene:MKS1
Gene Synonym:
Exon (16)1472..1554
Gene:MKS1
Gene Synonym:
Exon (17)1555..1652
Gene:MKS1
Gene Synonym:
Exon (18)1653..2387
Gene:MKS1
Gene Synonym:
Translation

Target ORF information:

RefSeq Version NM_001165927
Organism Homo sapiens (human)
Definition Homo sapiens Meckel syndrome, type 1 (MKS1), transcript variant 2, mRNA.

Target ORF information:

Epitope DYKDDDDK
Bacterial selection AMPR
Mammalian selection NeoR
Vector pcDNA3.1+/C-(K)DYK
NM_001165927

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
1501
1561
1621
ATGGCTGTGC CAGTTTCCTC ATTTGCACAG CGCACGAGGT CCCGCTTTCG AGTCCACCTG 
CAAAGAATCA CATCAAGCAA CTTTCTTCAT TATCAGCCTG CTGCCGAGCT CGGGAAGGAC
CTCATAGACT TGGCCACTTT TAGGCCTCAG CCAACTGCCA GTGGACACCG CCCAGAGGAA
GACGAAGAGG AGGAGATTGT GATTGGGTGG CAGGAGAAGC TCTTTAGCCA GTTTGAAGTA
GATCTGTACC AAAATGAAAC AGCCTGTCAG AGTCCTTTGG ATTATCAGTA CCGTCAGGAG
ATCCTGAAGC TGGAGAATTC GGGTGGCAAG AAAAACCGAC GAATCTTTAC CTACACTGAC
TCTGATAGAT ACACCAATTT GGAGGAGCAC TGTCAGAGAA TGACCACTGC AGCCAGCGAG
GTGCCTTCAT TCTTGGTCGA GCGAATGGCA AATGTCAGGC GTCGCCGGCA GGACAGGCGA
GGGATGGAGG GCGGCATCCT CAAGTCACGC ATCGTCACCT GGGAGCCCTC AGAAGAGTTT
GTCAGGAACA ACCACGTCAT TAACACCCCT CTTCAGACAA TGCACATCAT GGCAGACCTG
GGGCCCTATA AAAAGCTTGG CTATAAGAAG TATGAACATG TCCTGTGTAC TCTGAAGGTG
GATAGCAATG GTGTGATCAC AGTAAAGCCT GACTTCACGG GCCTCAAAGG ACCCTACAGG
ATTGAGACGG AGGGGGAGAA GCAGGAGCTG TGGAAATATA CGATCGACAA TGTTTCCCCC
CACGCACAGC CGGAGGAGGA GGAGCGGGAA CGGCGAGTGT TCAAGGATCT TTATGGCCGG
CACAAGGAGT ATCTCAGCAG CCTCGTAGGC ACCGACTTTG AGATGACTGT CCCAGGTGCC
CTCCGGCTCT TTGTAAATGG AGAGGTCGTT TCAGCCCAAG GCTATGAGTA TGACAATCTC
TACGTCCACT TCTTTGTAGA ATTGCCAACT GCTCACTGGT CAAGCCCAGC ATTCCAGCAG
CTCTCAGGAG TAACACAGAC CTGCACCACC AAGTCCCTGG CAATGGACAA GGTGGCTCAC
TTCTCCTACC CATTCACGTT TGAAGCCTTC TTCCTCCATG AGGATGAATC TTCTGATGCA
CTCCCGGAGT GGCCTGTGCT CTACTGTGAG GTCCTCTCGC TGGACTTCTG GCAGAGGTAC
CGTGTGGAAG GCTATGGGGC TGTGGTGCTG CCTGCCACTC CAGGCTCACA CACCCTGACA
GTCTCCACGT GGAGACCTGT GGAGCTTGGC ACGGTGGCTG AGCTGAGGAG GTTTTTCATT
GGCGGTTCTC TGGAACTGGA GGACCTCTCC TATGTACGGA TACCAGGATC CTTCAAGGGG
GAACGCCTGA GCCGCTTTGG ACTCCGCACA GAGACCACAG GCACTGTCAC CTTCCGCTTG
CACTGTCTGC AGCAGTCCAG GGCCTTCATG GAATCGAGCT CCCTTCAGAA AAGGATGCGG
AGTGTGTTGG ACCGTCTGGA AGGGTTCAGC CAGCAGAGTT CCATTCACAA TGTGCTAGAG
GCCTTCCGTC GAGCCCGGCG CCGCATGCAG GAGGCCCGGG AAAGCCTCCC GCAGGACCTA
GTGAGCCCCT CTGGAACCCT GGTCTCCTAG

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

 
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