FGFR1OP cDNA ORF clone, Homo sapiens(human)

Gene
Clones
gRNAs

Summary

Gene Symbol	FGFR1OP
Entrez Gene ID	11116
Full Name	FGFR1 oncogene partner
Synonyms	FOP
General protein information	Preferred Names FGFR1 oncogene partner Names FGFR1 oncogene partner fibroblast growth factor receptor 1 oncogene partner
Gene Type	protein-coding
Organism	Homo sapiens(human)
Genome	Chromosome: 6 Map Location: 6q27
Summary	This gene encodes a largely hydrophilic centrosomal protein that is required for anchoring microtubules to subcellular structures. A t(6;8)(q27;p11) chromosomal translocation, fusing this gene and the fibroblast growth factor receptor 1 (FGFR1) gene, has been found in cases of myeloproliferative disorder. The resulting chimeric protein contains the N-terminal leucine-rich region of this encoded protein fused to the catalytic domain of FGFR1. Alterations in this gene may also be associated with Crohn's disease, Graves' disease, and vitiligo. Alternatively spliced transcript variants that encode different proteins have been identified. [provided by RefSeq, Jul 2013].
Disorder MIM:	605392
Disorder Html:	Myeloproliferative disorder (2)

mRNA and Protein(s)

mRNA	Protein	Name
NM_007045.4	NP_008976.1	FGFR1 oncogene partner isoform a
NM_007045.3	NP_008976.1	FGFR1 oncogene partner isoform a
NM_001278690.1	NP_001265619.1	FGFR1 oncogene partner isoform c
NM_194429.2	NP_919410.1	FGFR1 oncogene partner isoform b
NM_194429.3	NP_919410.1	FGFR1 oncogene partner isoform b

Pathways from BioSystems

Homologies

Rattus norvegicus (Norway rat)	LOC683722	NP_001094478.1
Gallus gallus (chicken)	FGFR1OP	XP_419609.1
Danio rerio (zebrafish)	fgfr1op	NP_001002125.1
Mus musculus (house mouse)	Fgfr1op	NP_001183975.1
Pan troglodytes (chimpanzee)	FGFR1OP	XP_527596.3
Bos taurus (cattle)	FGFR1OP	NP_001071327.1
Xenopus tropicalis (tropical clawed frog)	fgfr1op	NP_001016758.1
Homo sapiens (human)	FGFR1OP	NP_008976.1
	FGFR1OP	XP_001102430.1
Canis lupus familiaris (dog)	FGFR1OP	XP_855273.2

Gene Ontology
Bibliography

Related articles in PubMed

The CEP19-RABL2 GTPase Complex Binds IFT-B to Initiate Intraflagellar Transport at the Ciliary Base.
Kanie T, Abbott KL, Mooney NA, Plowey ED, Demeter J, Jackson PK
Developmental cell42(1)22-36.e12(2017 07)

RABL2 interacts with the intraflagellar transport-B complex and CEP19 and participates in ciliary assembly.
Nishijima Y, Hagiya Y, Kubo T, Takei R, Katoh Y, Nakayama K
Molecular biology of the cell28(12)1652-1666(2017 Jun)

CEP19 cooperates with FOP and CEP350 to drive early steps in the ciliogenesis programme.
Mojarad BA, Gupta GD, Hasegan M, Goudiam O, Basto R, Gingras AC, Pelletier L
Open biology7(6)(2017 Jun)

Polymorphisms of the centrosomal gene (FGFR1OP) and lung cancer risk: a meta-analysis of 14,463 cases and 44,188 controls.
Kang X, Liu H, Onaitis MW, Liu Z, Owzar K, Han Y, Su L, Wei Y, Hung RJ, Brhane Y, McLaughlin J, Brennan P, Bickeb?ller H, Rosenberger A, Houlston RS, Caporaso N, Landi MT, Heinrich J, Risch A, Wu X, Ye Y, Christiani DC, Amos CI, Wei Q,
Carcinogenesis37(3)280-289(2016 Mar)

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

The rs151606 T>G was associated with an increased risk of lung cancer and rs12212247 T>C was associated with a decreased risk of lung cancer
Title: Polymorphisms of the centrosomal gene (FGFR1OP) and lung cancer risk: a meta-analysis of 14,463 cases and 44,188 controls.

FOP is a centriolar satellite protein involved in ciliogenesis.
Title: FOP is a centriolar satellite protein involved in ciliogenesis.

This study was designed to determine the association of CCR6 and FGFR10P (tag)single nucleotide polymorphisms with Vogt-Koyanagi-Harada (VKH) syndrome, in two independent Chinese Han populations.
Title: FGFR1OP tagSNP but not CCR6 polymorphisms are associated with Vogt-Koyanagi-Harada syndrome in Chinese Han.

Clinical trial of gene-disease association and gene-environment interaction. (HuGE Navigator)
Title: Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score.

Observational study and genome-wide association study of gene-disease association. (HuGE Navigator)
Title: Genome-wide association study for vitiligo identifies susceptibility loci at 6q27 and the MHC.

The following FGFR1OP gene cDNA ORF clone sequences were retrieved from the NCBI Reference Sequence Database (RefSeq). These sequences represent the protein coding region of the FGFR1OP 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	Accession No.	Definition	**Vector	*Turnaround time	Price (USD)
OHu00240	NM_194429.3 Latest version!	Homo sapiens FGFR1 oncogene partner (FGFR1OP), transcript variant 2, mRNA.	pcDNA3.1-C-(k)DYK or customized vector	7-9	$223.30 $319.00
OHu00349	NM_007045.4 Latest version!	Homo sapiens FGFR1 oncogene partner (FGFR1OP), transcript variant 1, mRNA.	pcDNA3.1-C-(k)DYK or customized vector	7-9	$237.30 $339.00
OHu01930	NM_001278690.1 Latest version!	Homo sapiens FGFR1 oncogene partner (FGFR1OP), transcript variant 3, mRNA.	pcDNA3.1-C-(k)DYK or customized vector	7-9	$223.30 $319.00
View Old Accession Versions >>
OHu00349	NM_007045.3	Homo sapiens FGFR1 oncogene partner (FGFR1OP), transcript variant 1, mRNA.	pcDNA3.1-C-(k)DYK or customized vector	7-9	$237.30 $339.00
OHu00240	NM_194429.2	Homo sapiens FGFR1 oncogene partner (FGFR1OP), transcript variant 2, mRNA.	pcDNA3.1-C-(k)DYK or customized vector	7-9	$223.30 $319.00
Hide Old Accession Versions >>

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** 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.

Reference Sequences (Refseq)

FGFR1OP ( NM_194429.2 ) cDNA ORF clone, Homo sapiens(human) -> NP_919410.1 Homo sapiens FGFR1 oncogene partner (FGFR1OP), transcript variant 2, mRNA.

Price & Availability↑

CloneID	OHu00240
Clone ID Related Accession (Same CDS sequence)	NM_194429.2 , NM_194429.3
Accession Version	NM_194429.2	Documents for ORF clone product in default vector
Sequence Information	ORF Nucleotide Sequence (Length: 1140bp) 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
Insert Structure	linear
Update Date	2019-02-23
Organism	Homo sapiens(human)
Product	FGFR1 oncogene partner isoform b
Comment	Comment: REVIEWED REFSEQ: This record has been curated by NCBI staff. The reference sequence was derived from DC418208.1, AK289846.1 and Z94721.1. On Jul 12, 2013 this sequence version replaced NM_194429.1. Transcript Variant: This variant (2) lacks an in-frame exon in the internal coding region, compared to variant 1. The encoded isoform (b) is shorter, compared to isoform a. 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 :: SRR1803611.156595.1, SRR1803611.10067.1 [ECO:0000332] RNAseq introns :: single sample supports all introns SAMEA1965299, SAMEA1966682 [ECO:0000348] ##Evidence-Data-END## COMPLETENESS: complete on the 3' end.

ATGGCGGCGA CGGCGGCCGC AGTGGTGGCC GAGGAGGACA CGGAGCTGCG GGACCTGCTG 
GTGCAGACGC TGGAGAACAG CGGGGTCCTG AACCGCATCA AGGCTGAACT CCGAGCAGCT 
GTGTTTTTAG CACTAGAGGA GCAAGAAAAA GTAGAGAACA AAACTCCTTT AGTTAATGAG 
AGCCTGAAAA AGTTTTTAAA TACCAAAGAC GGTCGTTTAG TGGCTAGTCT TGTTGCAGAA 
TTTCTTCAGT TTTTTAACCT TGACTTTACT TTGGCTGTTT TTCAACCTGA AACTAGCACA 
CTGCAAGGTC TCGAAGGTCG AGAGAATTTA GCCCGAGATT TAGGTATAAT TGAAGCAGAA 
GGTACTGTGG GTGGACCCTT ATTATTAGAA GTGATCAGGC GCTGTCAACA GAAAGAAAAA 
GGGCCAACCA CTGGGGAAGG TGCACTTGAT CTATCTGATG TACATTCTCC ACCAAAGTCA 
CCAGAGGGAA AAACAAGTGC ACAGACAACA CCAAGTAAGA AGGCCAATGA TGAGGCCAAT 
CAGAGTGATA CAAGTGTCTC CTTGTCAGAA CCCAAGAGCA AAAGCAGCCT TCACTTACTG 
TCCCATGAAA CAAAAATTGG ATCTTTTCTA AGCAACAGAA CTTTAGATGG CAAAGACAAA 
GCTGGCCTTT GTCCAGATGA AGATGATATG GAAGGAGATT CTTTCTTTGA TGATCCCATT 
CCTAAGCCAG AGAAAACTTA CGGTTTGAGG AAGGAACCTA GGAAGCAAGC AGGAAGTCTG 
GCCTCGCTCT CGGATGCACC CCCCTTAAAA AGTGGACTCA GCTCCCTGGC GGGAGCCCCT 
TCTTTAAAAG ACTCTGAGAG TAAAAGGGGA AATACAGTTT TGAAAGATCT GAAATTGATC 
AGTGATAAAA TTGGATCACT TGGATTAGGA ACTGGAGAAG ATGATGACTA TGTTGATGAT 
TTTAATAGTA CCAGCCATCG CTCAGAGAAA AGTGAGATAA GTATTGGTGA AGAGATAGAA 
GAAGACCTTT CTGTGGAAAT AGATGACATC AATACCAGTG ATAAGCTTGA TGACCTCACA 
CAAGATCTGA CTGTATCCCA GCTCAGTGAT GTTGCGGATT ATCTGGAAGA TGTTGCATAG

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

RefSeq	NP_919410.1
CDS	97..1236
Translation	MAATAAAVVAEEDTELRDLLVQTLENSGVLNRIKAELRAAVFLALEEQEKVENKTPLVNESLKKFLNTKDGRLVASLVAEFLQFFNLDFTLAVFQPETSTLQGLEGRENLARDLGIIEAEGTVGGPLLLEVIRRCQQKEKGPTTGEGALDLSDVHSPPKSPEGKTSAQTTPSKKANDEANQSDTSVSLSEPKSKSSLHLLSHETKIGSFLSNRTLDGKDKAGLCPDEDDMEGDSFFDDPIPKPEKTYGLRKEPRKQAGSLASLSDAPPLKSGLSSLAGAPSLKDSESKRGNTVLKDLKLISDKIGSLGLGTGEDDDYVDDFNSTSHRSEKSEISIGEEIEEDLSVEIDDINTSDKLDDLTQDLTVSQLSDVADYLEDVA

Target ORF information:

RefSeq Version	NM_194429.2
Organism	Homo sapiens(human)
Definition	Homo sapiens FGFR1 oncogene partner (FGFR1OP), transcript variant 2, mRNA.

Target ORF information:

Epitope	DYKDDDDK
Bacterial selection	AMP^R
Mammalian selection	Neo^R
Vector	pcDNA3.1⁺/C-(K)DYK

NM_194429.2

ORF Insert Sequence:

ATGGCGGCGA CGGCGGCCGC AGTGGTGGCC GAGGAGGACA CGGAGCTGCG GGACCTGCTG 
GTGCAGACGC TGGAGAACAG CGGGGTCCTG AACCGCATCA AGGCTGAACT CCGAGCAGCT 
GTGTTTTTAG CACTAGAGGA GCAAGAAAAA GTAGAGAACA AAACTCCTTT AGTTAATGAG 
AGCCTGAAAA AGTTTTTAAA TACCAAAGAC GGTCGTTTAG TGGCTAGTCT TGTTGCAGAA 
TTTCTTCAGT TTTTTAACCT TGACTTTACT TTGGCTGTTT TTCAACCTGA AACTAGCACA 
CTGCAAGGTC TCGAAGGTCG AGAGAATTTA GCCCGAGATT TAGGTATAAT TGAAGCAGAA 
GGTACTGTGG GTGGACCCTT ATTATTAGAA GTGATCAGGC GCTGTCAACA GAAAGAAAAA 
GGGCCAACCA CTGGGGAAGG TGCACTTGAT CTATCTGATG TACATTCTCC ACCAAAGTCA 
CCAGAGGGAA AAACAAGTGC ACAGACAACA CCAAGTAAGA AGGCCAATGA TGAGGCCAAT 
CAGAGTGATA CAAGTGTCTC CTTGTCAGAA CCCAAGAGCA AAAGCAGCCT TCACTTACTG 
TCCCATGAAA CAAAAATTGG ATCTTTTCTA AGCAACAGAA CTTTAGATGG CAAAGACAAA 
GCTGGCCTTT GTCCAGATGA AGATGATATG GAAGGAGATT CTTTCTTTGA TGATCCCATT 
CCTAAGCCAG AGAAAACTTA CGGTTTGAGG AAGGAACCTA GGAAGCAAGC AGGAAGTCTG 
GCCTCGCTCT CGGATGCACC CCCCTTAAAA AGTGGACTCA GCTCCCTGGC GGGAGCCCCT 
TCTTTAAAAG ACTCTGAGAG TAAAAGGGGA AATACAGTTT TGAAAGATCT GAAATTGATC 
AGTGATAAAA TTGGATCACT TGGATTAGGA ACTGGAGAAG ATGATGACTA TGTTGATGAT 
TTTAATAGTA CCAGCCATCG CTCAGAGAAA AGTGAGATAA GTATTGGTGA AGAGATAGAA 
GAAGACCTTT CTGTGGAAAT AGATGACATC AATACCAGTG ATAAGCTTGA TGACCTCACA 
CAAGATCTGA CTGTATCCCA GCTCAGTGAT GTTGCGGATT ATCTGGAAGA TGTTGCATAG

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

FGFR1OP ( NM_194429.3 ) cDNA ORF clone, Homo sapiens(human) -> NP_919410.1 Homo sapiens FGFR1 oncogene partner (FGFR1OP), transcript variant 2, mRNA.

Price & Availability↑

CloneID	OHu00240
Clone ID Related Accession (Same CDS sequence)	NM_194429.2 , NM_194429.3
Accession Version	NM_194429.3 Latest version!	Documents for ORF clone product in default vector
Sequence Information	ORF Nucleotide Sequence (Length: 1140bp) 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
Insert Structure	linear
Update Date	2019-05-31
Organism	Homo sapiens(human)
Product	FGFR1 oncogene partner isoform b
Comment	Comment: REVIEWED REFSEQ: This record has been curated by NCBI staff. The reference sequence was derived from AK289846.1 and Z94721.1. On Jun 1, 2019 this sequence version replaced NM_194429.2. Transcript Variant: This variant (2) lacks an in-frame exon in the internal coding region, compared to variant 1. The encoded isoform (b) is shorter, compared to isoform a. 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 :: SRR1803615.1715.1, SRR1803613.9872.1 [ECO:0000332] RNAseq introns :: single sample supports all introns SAMEA1965299, SAMEA1966682 [ECO:0000348] ##Evidence-Data-END## COMPLETENESS: complete on the 3' end.

ATGGCGGCGA CGGCGGCCGC AGTGGTGGCC GAGGAGGACA CGGAGCTGCG GGACCTGCTG 
GTGCAGACGC TGGAGAACAG CGGGGTCCTG AACCGCATCA AGGCTGAACT CCGAGCAGCT 
GTGTTTTTAG CACTAGAGGA GCAAGAAAAA GTAGAGAACA AAACTCCTTT AGTTAATGAG 
AGCCTGAAAA AGTTTTTAAA TACCAAAGAC GGTCGTTTAG TGGCTAGTCT TGTTGCAGAA 
TTTCTTCAGT TTTTTAACCT TGACTTTACT TTGGCTGTTT TTCAACCTGA AACTAGCACA 
CTGCAAGGTC TCGAAGGTCG AGAGAATTTA GCCCGAGATT TAGGTATAAT TGAAGCAGAA 
GGTACTGTGG GTGGACCCTT ATTATTAGAA GTGATCAGGC GCTGTCAACA GAAAGAAAAA 
GGGCCAACCA CTGGGGAAGG TGCACTTGAT CTATCTGATG TACATTCTCC ACCAAAGTCA 
CCAGAGGGAA AAACAAGTGC ACAGACAACA CCAAGTAAGA AGGCCAATGA TGAGGCCAAT 
CAGAGTGATA CAAGTGTCTC CTTGTCAGAA CCCAAGAGCA AAAGCAGCCT TCACTTACTG 
TCCCATGAAA CAAAAATTGG ATCTTTTCTA AGCAACAGAA CTTTAGATGG CAAAGACAAA 
GCTGGCCTTT GTCCAGATGA AGATGATATG GAAGGAGATT CTTTCTTTGA TGATCCCATT 
CCTAAGCCAG AGAAAACTTA CGGTTTGAGG AAGGAACCTA GGAAGCAAGC AGGAAGTCTG 
GCCTCGCTCT CGGATGCACC CCCCTTAAAA AGTGGACTCA GCTCCCTGGC GGGAGCCCCT 
TCTTTAAAAG ACTCTGAGAG TAAAAGGGGA AATACAGTTT TGAAAGATCT GAAATTGATC 
AGTGATAAAA TTGGATCACT TGGATTAGGA ACTGGAGAAG ATGATGACTA TGTTGATGAT 
TTTAATAGTA CCAGCCATCG CTCAGAGAAA AGTGAGATAA GTATTGGTGA AGAGATAGAA 
GAAGACCTTT CTGTGGAAAT AGATGACATC AATACCAGTG ATAAGCTTGA TGACCTCACA 
CAAGATCTGA CTGTATCCCA GCTCAGTGAT GTTGCGGATT ATCTGGAAGA TGTTGCATAG

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

RefSeq	NP_919410.1
CDS	17..1156
Translation	MAATAAAVVAEEDTELRDLLVQTLENSGVLNRIKAELRAAVFLALEEQEKVENKTPLVNESLKKFLNTKDGRLVASLVAEFLQFFNLDFTLAVFQPETSTLQGLEGRENLARDLGIIEAEGTVGGPLLLEVIRRCQQKEKGPTTGEGALDLSDVHSPPKSPEGKTSAQTTPSKKANDEANQSDTSVSLSEPKSKSSLHLLSHETKIGSFLSNRTLDGKDKAGLCPDEDDMEGDSFFDDPIPKPEKTYGLRKEPRKQAGSLASLSDAPPLKSGLSSLAGAPSLKDSESKRGNTVLKDLKLISDKIGSLGLGTGEDDDYVDDFNSTSHRSEKSEISIGEEIEEDLSVEIDDINTSDKLDDLTQDLTVSQLSDVADYLEDVA

Target ORF information:

RefSeq Version	NM_194429.3
Organism	Homo sapiens(human)
Definition	Homo sapiens FGFR1 oncogene partner (FGFR1OP), transcript variant 2, mRNA.

Target ORF information:

Epitope	DYKDDDDK
Bacterial selection	AMP^R
Mammalian selection	Neo^R
Vector	pcDNA3.1⁺/C-(K)DYK

NM_194429.3

ORF Insert Sequence:

ATGGCGGCGA CGGCGGCCGC AGTGGTGGCC GAGGAGGACA CGGAGCTGCG GGACCTGCTG 
GTGCAGACGC TGGAGAACAG CGGGGTCCTG AACCGCATCA AGGCTGAACT CCGAGCAGCT 
GTGTTTTTAG CACTAGAGGA GCAAGAAAAA GTAGAGAACA AAACTCCTTT AGTTAATGAG 
AGCCTGAAAA AGTTTTTAAA TACCAAAGAC GGTCGTTTAG TGGCTAGTCT TGTTGCAGAA 
TTTCTTCAGT TTTTTAACCT TGACTTTACT TTGGCTGTTT TTCAACCTGA AACTAGCACA 
CTGCAAGGTC TCGAAGGTCG AGAGAATTTA GCCCGAGATT TAGGTATAAT TGAAGCAGAA 
GGTACTGTGG GTGGACCCTT ATTATTAGAA GTGATCAGGC GCTGTCAACA GAAAGAAAAA 
GGGCCAACCA CTGGGGAAGG TGCACTTGAT CTATCTGATG TACATTCTCC ACCAAAGTCA 
CCAGAGGGAA AAACAAGTGC ACAGACAACA CCAAGTAAGA AGGCCAATGA TGAGGCCAAT 
CAGAGTGATA CAAGTGTCTC CTTGTCAGAA CCCAAGAGCA AAAGCAGCCT TCACTTACTG 
TCCCATGAAA CAAAAATTGG ATCTTTTCTA AGCAACAGAA CTTTAGATGG CAAAGACAAA 
GCTGGCCTTT GTCCAGATGA AGATGATATG GAAGGAGATT CTTTCTTTGA TGATCCCATT 
CCTAAGCCAG AGAAAACTTA CGGTTTGAGG AAGGAACCTA GGAAGCAAGC AGGAAGTCTG 
GCCTCGCTCT CGGATGCACC CCCCTTAAAA AGTGGACTCA GCTCCCTGGC GGGAGCCCCT 
TCTTTAAAAG ACTCTGAGAG TAAAAGGGGA AATACAGTTT TGAAAGATCT GAAATTGATC 
AGTGATAAAA TTGGATCACT TGGATTAGGA ACTGGAGAAG ATGATGACTA TGTTGATGAT 
TTTAATAGTA CCAGCCATCG CTCAGAGAAA AGTGAGATAA GTATTGGTGA AGAGATAGAA 
GAAGACCTTT CTGTGGAAAT AGATGACATC AATACCAGTG ATAAGCTTGA TGACCTCACA 
CAAGATCTGA CTGTATCCCA GCTCAGTGAT GTTGCGGATT ATCTGGAAGA TGTTGCATAG

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

FGFR1OP ( NM_007045.4 ) cDNA ORF clone, Homo sapiens(human) -> NP_008976.1 Homo sapiens FGFR1 oncogene partner (FGFR1OP), transcript variant 1, mRNA.

Price & Availability↑

CloneID	OHu00349
Clone ID Related Accession (Same CDS sequence)	NM_007045.4 , NM_007045.3
Accession Version	NM_007045.4 Latest version!	Documents for ORF clone product in default vector
Sequence Information	ORF Nucleotide Sequence (Length: 1200bp) 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
Insert Structure	linear
Update Date	2019-12-30
Organism	Homo sapiens(human)
Product	FGFR1 oncogene partner isoform a
Comment	Comment: REVIEWED REFSEQ: This record has been curated by NCBI staff. The reference sequence was derived from DC418208.1, AK312791.1 and Z94721.1. On Nov 23, 2018 this sequence version replaced NM_007045.3. Transcript Variant: This variant (1) represents the longest transcript and encodes the longest isoform (a). 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 :: SRR1803617.246086.1, SRR1803615.81276.1 [ECO:0000332] RNAseq introns :: single sample supports all introns SAMEA1965299, SAMEA1966682 [ECO:0000348] ##Evidence-Data-END## ##RefSeq-Attributes-START## MANE Ensembl match :: ENST00000366847.9/ ENSP00000355812.3 RefSeq Select criteria :: based on conservation, expression, longest protein ##RefSeq-Attributes-END## COMPLETENESS: full length.

ATGGCGGCGA CGGCGGCCGC AGTGGTGGCC GAGGAGGACA CGGAGCTGCG GGACCTGCTG 
GTGCAGACGC TGGAGAACAG CGGGGTCCTG AACCGCATCA AGGCTGAACT CCGAGCAGCT 
GTGTTTTTAG CACTAGAGGA GCAAGAAAAA GTAGAGAACA AAACTCCTTT AGTTAATGAG 
AGCCTGAAAA AGTTTTTAAA TACCAAAGAC GGTCGTTTAG TGGCTAGTCT TGTTGCAGAA 
TTTCTTCAGT TTTTTAACCT TGACTTTACT TTGGCTGTTT TTCAACCTGA AACTAGCACA 
CTGCAAGGTC TCGAAGGTCG AGAGAATTTA GCCCGAGATT TAGGTATAAT TGAAGCAGAA 
GGTACTGTGG GTGGACCCTT ATTATTAGAA GTGATCAGGC GCTGTCAACA GAAAGAAAAA 
GGGCCAACCA CTGGGGAAGG TGCACTTGAT CTATCTGATG TACATTCTCC ACCAAAGTCA 
CCAGAGGGAA AAACAAGTGC ACAGACAACA CCAAGTAAGA TACCAAGGTA TAAAGGACAA 
GGTAAGAAGA AGACAAGCGG GCAGAAGGCT GGTGACAAGA AGGCCAATGA TGAGGCCAAT 
CAGAGTGATA CAAGTGTCTC CTTGTCAGAA CCCAAGAGCA AAAGCAGCCT TCACTTACTG 
TCCCATGAAA CAAAAATTGG ATCTTTTCTA AGCAACAGAA CTTTAGATGG CAAAGACAAA 
GCTGGCCTTT GTCCAGATGA AGATGATATG GAAGGAGATT CTTTCTTTGA TGATCCCATT 
CCTAAGCCAG AGAAAACTTA CGGTTTGAGG AAGGAACCTA GGAAGCAAGC AGGAAGTCTG 
GCCTCGCTCT CGGATGCACC CCCCTTAAAA AGTGGACTCA GCTCCCTGGC GGGAGCCCCT 
TCTTTAAAAG ACTCTGAGAG TAAAAGGGGA AATACAGTTT TGAAAGATCT GAAATTGATC 
AGTGATAAAA TTGGATCACT TGGATTAGGA ACTGGAGAAG ATGATGACTA TGTTGATGAT 
TTTAATAGTA CCAGCCATCG CTCAGAGAAA AGTGAGATAA GTATTGGTGA AGAGATAGAA 
GAAGACCTTT CTGTGGAAAT AGATGACATC AATACCAGTG ATAAGCTTGA TGACCTCACA 
CAAGATCTGA CTGTATCCCA GCTCAGTGAT GTTGCGGATT ATCTGGAAGA TGTTGCATAG

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

RefSeq	NP_008976.1
CDS	17..1216
Translation	MAATAAAVVAEEDTELRDLLVQTLENSGVLNRIKAELRAAVFLALEEQEKVENKTPLVNESLKKFLNTKDGRLVASLVAEFLQFFNLDFTLAVFQPETSTLQGLEGRENLARDLGIIEAEGTVGGPLLLEVIRRCQQKEKGPTTGEGALDLSDVHSPPKSPEGKTSAQTTPSKIPRYKGQGKKKTSGQKAGDKKANDEANQSDTSVSLSEPKSKSSLHLLSHETKIGSFLSNRTLDGKDKAGLCPDEDDMEGDSFFDDPIPKPEKTYGLRKEPRKQAGSLASLSDAPPLKSGLSSLAGAPSLKDSESKRGNTVLKDLKLISDKIGSLGLGTGEDDDYVDDFNSTSHRSEKSEISIGEEIEEDLSVEIDDINTSDKLDDLTQDLTVSQLSDVADYLEDVA

Target ORF information:

RefSeq Version	NM_007045.4
Organism	Homo sapiens(human)
Definition	Homo sapiens FGFR1 oncogene partner (FGFR1OP), transcript variant 1, mRNA.

Target ORF information:

Epitope	DYKDDDDK
Bacterial selection	AMP^R
Mammalian selection	Neo^R
Vector	pcDNA3.1⁺/C-(K)DYK

NM_007045.4

ORF Insert Sequence:

ATGGCGGCGA CGGCGGCCGC AGTGGTGGCC GAGGAGGACA CGGAGCTGCG GGACCTGCTG 
GTGCAGACGC TGGAGAACAG CGGGGTCCTG AACCGCATCA AGGCTGAACT CCGAGCAGCT 
GTGTTTTTAG CACTAGAGGA GCAAGAAAAA GTAGAGAACA AAACTCCTTT AGTTAATGAG 
AGCCTGAAAA AGTTTTTAAA TACCAAAGAC GGTCGTTTAG TGGCTAGTCT TGTTGCAGAA 
TTTCTTCAGT TTTTTAACCT TGACTTTACT TTGGCTGTTT TTCAACCTGA AACTAGCACA 
CTGCAAGGTC TCGAAGGTCG AGAGAATTTA GCCCGAGATT TAGGTATAAT TGAAGCAGAA 
GGTACTGTGG GTGGACCCTT ATTATTAGAA GTGATCAGGC GCTGTCAACA GAAAGAAAAA 
GGGCCAACCA CTGGGGAAGG TGCACTTGAT CTATCTGATG TACATTCTCC ACCAAAGTCA 
CCAGAGGGAA AAACAAGTGC ACAGACAACA CCAAGTAAGA TACCAAGGTA TAAAGGACAA 
GGTAAGAAGA AGACAAGCGG GCAGAAGGCT GGTGACAAGA AGGCCAATGA TGAGGCCAAT 
CAGAGTGATA CAAGTGTCTC CTTGTCAGAA CCCAAGAGCA AAAGCAGCCT TCACTTACTG 
TCCCATGAAA CAAAAATTGG ATCTTTTCTA AGCAACAGAA CTTTAGATGG CAAAGACAAA 
GCTGGCCTTT GTCCAGATGA AGATGATATG GAAGGAGATT CTTTCTTTGA TGATCCCATT 
CCTAAGCCAG AGAAAACTTA CGGTTTGAGG AAGGAACCTA GGAAGCAAGC AGGAAGTCTG 
GCCTCGCTCT CGGATGCACC CCCCTTAAAA AGTGGACTCA GCTCCCTGGC GGGAGCCCCT 
TCTTTAAAAG ACTCTGAGAG TAAAAGGGGA AATACAGTTT TGAAAGATCT GAAATTGATC 
AGTGATAAAA TTGGATCACT TGGATTAGGA ACTGGAGAAG ATGATGACTA TGTTGATGAT 
TTTAATAGTA CCAGCCATCG CTCAGAGAAA AGTGAGATAA GTATTGGTGA AGAGATAGAA 
GAAGACCTTT CTGTGGAAAT AGATGACATC AATACCAGTG ATAAGCTTGA TGACCTCACA 
CAAGATCTGA CTGTATCCCA GCTCAGTGAT GTTGCGGATT ATCTGGAAGA TGTTGCATAG

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

FGFR1OP ( NM_007045.3 ) cDNA ORF clone, Homo sapiens(human) -> NP_008976.1 Homo sapiens FGFR1 oncogene partner (FGFR1OP), transcript variant 1, mRNA.

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CloneID	OHu00349
Clone ID Related Accession (Same CDS sequence)	NM_007045.4 , NM_007045.3
Accession Version	NM_007045.3	Documents for ORF clone product in default vector
Sequence Information	ORF Nucleotide Sequence (Length: 1200bp) 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
Insert Structure	linear
Update Date	2017-11-11
Organism	Homo sapiens(human)
Product	FGFR1 oncogene partner isoform a
Comment	Comment: REVIEWED REFSEQ: This record has been curated by NCBI staff. The reference sequence was derived from DC418208.1, AK312791.1 and Z94721.1. On Jul 12, 2013 this sequence version replaced NM_007045.2. Transcript Variant: This variant (1) represents the longest transcript and encodes the longest isoform (a). 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 :: SRR1660809.77525.1, SRR1803617.246086.1 [ECO:0000332] RNAseq introns :: single sample supports all introns SAMEA1965299, SAMEA1966682 [ECO:0000348] ##Evidence-Data-END## COMPLETENESS: complete on the 3' end.

ATGGCGGCGA CGGCGGCCGC AGTGGTGGCC GAGGAGGACA CGGAGCTGCG GGACCTGCTG 
GTGCAGACGC TGGAGAACAG CGGGGTCCTG AACCGCATCA AGGCTGAACT CCGAGCAGCT 
GTGTTTTTAG CACTAGAGGA GCAAGAAAAA GTAGAGAACA AAACTCCTTT AGTTAATGAG 
AGCCTGAAAA AGTTTTTAAA TACCAAAGAC GGTCGTTTAG TGGCTAGTCT TGTTGCAGAA 
TTTCTTCAGT TTTTTAACCT TGACTTTACT TTGGCTGTTT TTCAACCTGA AACTAGCACA 
CTGCAAGGTC TCGAAGGTCG AGAGAATTTA GCCCGAGATT TAGGTATAAT TGAAGCAGAA 
GGTACTGTGG GTGGACCCTT ATTATTAGAA GTGATCAGGC GCTGTCAACA GAAAGAAAAA 
GGGCCAACCA CTGGGGAAGG TGCACTTGAT CTATCTGATG TACATTCTCC ACCAAAGTCA 
CCAGAGGGAA AAACAAGTGC ACAGACAACA CCAAGTAAGA TACCAAGGTA TAAAGGACAA 
GGTAAGAAGA AGACAAGCGG GCAGAAGGCT GGTGACAAGA AGGCCAATGA TGAGGCCAAT 
CAGAGTGATA CAAGTGTCTC CTTGTCAGAA CCCAAGAGCA AAAGCAGCCT TCACTTACTG 
TCCCATGAAA CAAAAATTGG ATCTTTTCTA AGCAACAGAA CTTTAGATGG CAAAGACAAA 
GCTGGCCTTT GTCCAGATGA AGATGATATG GAAGGAGATT CTTTCTTTGA TGATCCCATT 
CCTAAGCCAG AGAAAACTTA CGGTTTGAGG AAGGAACCTA GGAAGCAAGC AGGAAGTCTG 
GCCTCGCTCT CGGATGCACC CCCCTTAAAA AGTGGACTCA GCTCCCTGGC GGGAGCCCCT 
TCTTTAAAAG ACTCTGAGAG TAAAAGGGGA AATACAGTTT TGAAAGATCT GAAATTGATC 
AGTGATAAAA TTGGATCACT TGGATTAGGA ACTGGAGAAG ATGATGACTA TGTTGATGAT 
TTTAATAGTA CCAGCCATCG CTCAGAGAAA AGTGAGATAA GTATTGGTGA AGAGATAGAA 
GAAGACCTTT CTGTGGAAAT AGATGACATC AATACCAGTG ATAAGCTTGA TGACCTCACA 
CAAGATCTGA CTGTATCCCA GCTCAGTGAT GTTGCGGATT ATCTGGAAGA TGTTGCATAG

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

RefSeq	NP_008976.1
CDS	97..1296
Translation	MAATAAAVVAEEDTELRDLLVQTLENSGVLNRIKAELRAAVFLALEEQEKVENKTPLVNESLKKFLNTKDGRLVASLVAEFLQFFNLDFTLAVFQPETSTLQGLEGRENLARDLGIIEAEGTVGGPLLLEVIRRCQQKEKGPTTGEGALDLSDVHSPPKSPEGKTSAQTTPSKIPRYKGQGKKKTSGQKAGDKKANDEANQSDTSVSLSEPKSKSSLHLLSHETKIGSFLSNRTLDGKDKAGLCPDEDDMEGDSFFDDPIPKPEKTYGLRKEPRKQAGSLASLSDAPPLKSGLSSLAGAPSLKDSESKRGNTVLKDLKLISDKIGSLGLGTGEDDDYVDDFNSTSHRSEKSEISIGEEIEEDLSVEIDDINTSDKLDDLTQDLTVSQLSDVADYLEDVA

Target ORF information:

RefSeq Version	NM_007045.3
Organism	Homo sapiens(human)
Definition	Homo sapiens FGFR1 oncogene partner (FGFR1OP), transcript variant 1, mRNA.

Target ORF information:

Epitope	DYKDDDDK
Bacterial selection	AMP^R
Mammalian selection	Neo^R
Vector	pcDNA3.1⁺/C-(K)DYK

NM_007045.3

ORF Insert Sequence:

ATGGCGGCGA CGGCGGCCGC AGTGGTGGCC GAGGAGGACA CGGAGCTGCG GGACCTGCTG 
GTGCAGACGC TGGAGAACAG CGGGGTCCTG AACCGCATCA AGGCTGAACT CCGAGCAGCT 
GTGTTTTTAG CACTAGAGGA GCAAGAAAAA GTAGAGAACA AAACTCCTTT AGTTAATGAG 
AGCCTGAAAA AGTTTTTAAA TACCAAAGAC GGTCGTTTAG TGGCTAGTCT TGTTGCAGAA 
TTTCTTCAGT TTTTTAACCT TGACTTTACT TTGGCTGTTT TTCAACCTGA AACTAGCACA 
CTGCAAGGTC TCGAAGGTCG AGAGAATTTA GCCCGAGATT TAGGTATAAT TGAAGCAGAA 
GGTACTGTGG GTGGACCCTT ATTATTAGAA GTGATCAGGC GCTGTCAACA GAAAGAAAAA 
GGGCCAACCA CTGGGGAAGG TGCACTTGAT CTATCTGATG TACATTCTCC ACCAAAGTCA 
CCAGAGGGAA AAACAAGTGC ACAGACAACA CCAAGTAAGA TACCAAGGTA TAAAGGACAA 
GGTAAGAAGA AGACAAGCGG GCAGAAGGCT GGTGACAAGA AGGCCAATGA TGAGGCCAAT 
CAGAGTGATA CAAGTGTCTC CTTGTCAGAA CCCAAGAGCA AAAGCAGCCT TCACTTACTG 
TCCCATGAAA CAAAAATTGG ATCTTTTCTA AGCAACAGAA CTTTAGATGG CAAAGACAAA 
GCTGGCCTTT GTCCAGATGA AGATGATATG GAAGGAGATT CTTTCTTTGA TGATCCCATT 
CCTAAGCCAG AGAAAACTTA CGGTTTGAGG AAGGAACCTA GGAAGCAAGC AGGAAGTCTG 
GCCTCGCTCT CGGATGCACC CCCCTTAAAA AGTGGACTCA GCTCCCTGGC GGGAGCCCCT 
TCTTTAAAAG ACTCTGAGAG TAAAAGGGGA AATACAGTTT TGAAAGATCT GAAATTGATC 
AGTGATAAAA TTGGATCACT TGGATTAGGA ACTGGAGAAG ATGATGACTA TGTTGATGAT 
TTTAATAGTA CCAGCCATCG CTCAGAGAAA AGTGAGATAA GTATTGGTGA AGAGATAGAA 
GAAGACCTTT CTGTGGAAAT AGATGACATC AATACCAGTG ATAAGCTTGA TGACCTCACA 
CAAGATCTGA CTGTATCCCA GCTCAGTGAT GTTGCGGATT ATCTGGAAGA TGTTGCATAG

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

FGFR1OP ( NM_001278690.1 ) cDNA ORF clone, Homo sapiens(human) -> NP_001265619.1 Homo sapiens FGFR1 oncogene partner (FGFR1OP), transcript variant 3, mRNA.

Price & Availability↑

CloneID	OHu01930
Clone ID Related Accession (Same CDS sequence)	NM_001278690.1
Accession Version	NM_001278690.1 Latest version!	Documents for ORF clone product in default vector
Sequence Information	ORF Nucleotide Sequence (Length: 1056bp) 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
Insert Structure	linear
Update Date	2019-04-01
Organism	Homo sapiens(human)
Product	FGFR1 oncogene partner isoform c
Comment	Comment: REVIEWED REFSEQ: This record has been curated by NCBI staff. The reference sequence was derived from DC418208.1, AK294950.1 and Z94721.1. Transcript Variant: This variant (3) lacks two consecutive in-frame exons in the internal coding region, and uses an alternate splice site at the 3'-terminal exon, compared to variant 1. The encoded isoform (c) is shorter and has a distinct C-terminus, compared to isoform a. 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 :: AK294950.1 [ECO:0000332] RNAseq introns :: single sample supports all introns SAMEA1968968, SAMEA2148093 [ECO:0000348] ##Evidence-Data-END## COMPLETENESS: complete on the 3' end.

ATGGCGGCGA CGGCGGCCGC AGTGGTGGCC GAGGAGGACA CGGAGCTGCG GGACCTGCTG 
GTGCAGACGC TGGAGAACAG CGGGGTCCTG AACCGCATCA AGGCTGAACT CCGAGCAGCT 
GTGTTTTTAG CACTAGAGGA GCAAGAAAAA GTAGAGAACA AAACTCCTTT AGTTAATGAG 
AGCCTGAAAA AGTTTTTAAA TACCAAAGAC GGTCGTTTAG TGGCTAGTCT TGTTGCAGAA 
TTTCTTCAGT TTTTTAACCT TGACTTTACT TTGGCTGTTT TTCAACCTGA AACTAGCACA 
CTGCAAGGTC TCGAAGGTCG AGAGAATTTA GCCCGAGATT TAGGTATAAT TGAAGCAGAA 
GGTACTGTGG GTGGACCCTT ATTATTAGAA GTGATCAGGC GCTGTCAACA GAAAGAAAAA 
GGGCCAACCA CTGGGGAAAA GGCCAATGAT GAGGCCAATC AGAGTGATAC AAGTGTCTCC 
TTGTCAGAAC CCAAGAGCAA AAGCAGCCTT CACTTACTGT CCCATGAAAC AAAAATTGGA 
TCTTTTCTAA GCAACAGAAC TTTAGATGGC AAAGACAAAG CTGGCCTTTG TCCAGATGAA 
GATGATATGG AAGGAGATTC TTTCTTTGAT GATCCCATTC CTAAGCCAGA GAAAACTTAC 
GGTTTGAGGA AGGAACCTAG GAAGCAAGCA GGAAGTCTGG CCTCGCTCTC GGATGCACCC 
CCCTTAAAAA GTGGACTCAG CTCCCTGGCG GGAGCCCCTT CTTTAAAAGA CTCTGAGAGT 
AAAAGGGGAA ATACAGTTTT GAAAGATCTG AAATTGATCA GTGATAAAAT TGGATCACTT 
GGATTAGGAA CTGGAGAAGA TGATGACTAT GTTGATGATT TTAATAGTAC CAGCCATCGC 
TCAGAGAAAA GTGAGATAAG TATTGGTGAA GAGATAGAAG AAGACCTTTC TGTGGAAATA 
GATGACATCA ATACCAGTGA TAAGACAATC ACTCAGCTGG AATGTCTGCT CTCTATTGGT 
GCCTTGCATT TCAAAAACAC TGCAGATATT TTTTAA

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

RefSeq	NP_001265619.1
CDS	97..1152
Translation	MAATAAAVVAEEDTELRDLLVQTLENSGVLNRIKAELRAAVFLALEEQEKVENKTPLVNESLKKFLNTKDGRLVASLVAEFLQFFNLDFTLAVFQPETSTLQGLEGRENLARDLGIIEAEGTVGGPLLLEVIRRCQQKEKGPTTGEKANDEANQSDTSVSLSEPKSKSSLHLLSHETKIGSFLSNRTLDGKDKAGLCPDEDDMEGDSFFDDPIPKPEKTYGLRKEPRKQAGSLASLSDAPPLKSGLSSLAGAPSLKDSESKRGNTVLKDLKLISDKIGSLGLGTGEDDDYVDDFNSTSHRSEKSEISIGEEIEEDLSVEIDDINTSDKTITQLECLLSIGALHFKNTADIF

Target ORF information:

RefSeq Version	NM_001278690.1
Organism	Homo sapiens(human)
Definition	Homo sapiens FGFR1 oncogene partner (FGFR1OP), transcript variant 3, mRNA.

Target ORF information:

Epitope	DYKDDDDK
Bacterial selection	AMP^R
Mammalian selection	Neo^R
Vector	pcDNA3.1⁺/C-(K)DYK

NM_001278690.1

ORF Insert Sequence:

ATGGCGGCGA CGGCGGCCGC AGTGGTGGCC GAGGAGGACA CGGAGCTGCG GGACCTGCTG 
GTGCAGACGC TGGAGAACAG CGGGGTCCTG AACCGCATCA AGGCTGAACT CCGAGCAGCT 
GTGTTTTTAG CACTAGAGGA GCAAGAAAAA GTAGAGAACA AAACTCCTTT AGTTAATGAG 
AGCCTGAAAA AGTTTTTAAA TACCAAAGAC GGTCGTTTAG TGGCTAGTCT TGTTGCAGAA 
TTTCTTCAGT TTTTTAACCT TGACTTTACT TTGGCTGTTT TTCAACCTGA AACTAGCACA 
CTGCAAGGTC TCGAAGGTCG AGAGAATTTA GCCCGAGATT TAGGTATAAT TGAAGCAGAA 
GGTACTGTGG GTGGACCCTT ATTATTAGAA GTGATCAGGC GCTGTCAACA GAAAGAAAAA 
GGGCCAACCA CTGGGGAAAA GGCCAATGAT GAGGCCAATC AGAGTGATAC AAGTGTCTCC 
TTGTCAGAAC CCAAGAGCAA AAGCAGCCTT CACTTACTGT CCCATGAAAC AAAAATTGGA 
TCTTTTCTAA GCAACAGAAC TTTAGATGGC AAAGACAAAG CTGGCCTTTG TCCAGATGAA 
GATGATATGG AAGGAGATTC TTTCTTTGAT GATCCCATTC CTAAGCCAGA GAAAACTTAC 
GGTTTGAGGA AGGAACCTAG GAAGCAAGCA GGAAGTCTGG CCTCGCTCTC GGATGCACCC 
CCCTTAAAAA GTGGACTCAG CTCCCTGGCG GGAGCCCCTT CTTTAAAAGA CTCTGAGAGT 
AAAAGGGGAA ATACAGTTTT GAAAGATCTG AAATTGATCA GTGATAAAAT TGGATCACTT 
GGATTAGGAA CTGGAGAAGA TGATGACTAT GTTGATGATT TTAATAGTAC CAGCCATCGC 
TCAGAGAAAA GTGAGATAAG TATTGGTGAA GAGATAGAAG AAGACCTTTC TGTGGAAATA 
GATGACATCA ATACCAGTGA TAAGACAATC ACTCAGCTGG AATGTCTGCT CTCTATTGGT 
GCCTTGCATT TCAAAAACAC TGCAGATATT TTTTAA

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

PubMed

The CEP19-RABL2 GTPase Complex Binds IFT-B to Initiate Intraflagellar Transport at the Ciliary Base.
Developmental cell42(1)22-36.e12(2017 07)
Kanie T,Abbott KL,Mooney NA,Plowey ED,Demeter J,Jackson PK

RABL2 interacts with the intraflagellar transport-B complex and CEP19 and participates in ciliary assembly.
Molecular biology of the cell28(12)1652-1666(2017 Jun)
Nishijima Y,Hagiya Y,Kubo T,Takei R,Katoh Y,Nakayama K

CEP19 cooperates with FOP and CEP350 to drive early steps in the ciliogenesis programme.
Open biology7(6)(2017 Jun)
Mojarad BA,Gupta GD,Hasegan M,Goudiam O,Basto R,Gingras AC,Pelletier L

Polymorphisms of the centrosomal gene (FGFR1OP) and lung cancer risk: a meta-analysis of 14,463 cases and 44,188 controls.
Carcinogenesis37(3)280-289(2016 Mar)
Kang X,Liu H,Onaitis MW,Liu Z,Owzar K,Han Y,Su L,Wei Y,Hung RJ,Brhane Y,McLaughlin J,Brennan P,Bickeb?ller H,Rosenberger A,Houlston RS,Caporaso N,Landi MT,Heinrich J,Risch A,Wu X,Ye Y,Christiani DC,Amos CI,Wei Q,

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FGFR1OP cDNA ORF clone, Homo sapiens(human)

Gene

Clones

gRNAs

Related articles in PubMed

Target ORF information:

Target ORF information:

ORF Insert Sequence:

Target ORF information:

Target ORF information:

ORF Insert Sequence:

Target ORF information:

Target ORF information:

ORF Insert Sequence:

Target ORF information:

Target ORF information:

ORF Insert Sequence:

Target ORF information:

Target ORF information:

ORF Insert Sequence:

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