FAM47E-STBD1 cDNA ORF clone, Homo sapiens(human)

Gene
Clones
gRNAs

Summary

Gene Symbol	FAM47E-STBD1
Entrez Gene ID	100631383
Full Name	FAM47E-STBD1 readthrough
General protein information	Preferred Names FAM47E-STBD1 readthrough Names uncharacterized protein LOC100631383
Gene Type	protein-coding
Organism	Homo sapiens(human)
Genome	Chromosome: 4 Map Location: 4q21.1
Summary	This locus represents naturally occurring read-through transcription between the neighboring FAM47E (family with sequence similarity 47, member E) and STBD1 (starch binding domain 1) genes on chromosome 4. The read-through transcript encodes a protein that shares sequence identity with the upstream gene product but its C-terminal region is distinct due to frameshifts relative to the downstream gene. [provided by RefSeq, Jul 2011].

mRNA and Protein(s)

mRNA	Protein	Name
NM_001242939.1	NP_001229868.1	uncharacterized protein LOC100631383

Pathways from BioSystems
Gene Ontology
Bibliography

Related articles in PubMed

Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease.
Nalls MA, Pankratz N, Lill CM, Do CB, Hernandez DG, Saad M, DeStefano AL, Kara E, Bras J, Sharma M, Schulte C, Keller MF, Arepalli S, Letson C, Edsall C, Stefansson H, Liu X, Pliner H, Lee JH, Cheng R, , , , , , , , , , , , , Ikram MA, Ioannidis JP, Hadjigeorgiou GM, Bis JC, Martinez M, Perlmutter JS, Goate A, Marder K, Fiske B, Sutherland M, Xiromerisiou G, Myers RH, Clark LN, Stefansson K, Hardy JA, Heutink P, Chen H, Wood NW, Houlden H, Payami H, Brice A, Scott WK, Gasser T, Bertram L, Eriksson N, Foroud T, Singleton AB
Nature genetics46(9)989-93(2014 Sep)

Web-based genome-wide association study identifies two novel loci and a substantial genetic component for Parkinson's disease.
Do CB, Tung JY, Dorfman E, Kiefer AK, Drabant EM, Francke U, Mountain JL, Goldman SM, Tanner CM, Langston JW, Wojcicki A, Eriksson N
PLoS genetics7(6)e1002141(2011 Jun)

Expression of conjoined genes: another mechanism for gene regulation in eukaryotes.
Prakash T, Sharma VK, Adati N, Ozawa R, Kumar N, Nishida Y, Fujikake T, Takeda T, Taylor TD
PloS one5(10)e13284(2010 Oct)

Genome-wide association study reveals genetic risk underlying Parkinson's disease.
Sim?n-S?nchez J, Schulte C, Bras JM, Sharma M, Gibbs JR, Berg D, Paisan-Ruiz C, Lichtner P, Scholz SW, Hernandez DG, Kr?ger R, Federoff M, Klein C, Goate A, Perlmutter J, Bonin M, Nalls MA, Illig T, Gieger C, Houlden H, Steffens M, Okun MS, Racette BA, Cookson MR, Foote KD, Fernandez HH, Traynor BJ, Schreiber S, Arepalli S, Zonozi R, Gwinn K, van der Brug M, Lopez G, Chanock SJ, Schatzkin A, Park Y, Hollenbeck A, Gao J, Huang X, Wood NW, Lorenz D, Deuschl G, Chen H, Riess O, Hardy JA, Singleton AB, Gasser T
Nature genetics41(12)1308-12(2009 Dec)

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

The following FAM47E-STBD1 gene cDNA ORF clone sequences were retrieved from the NCBI Reference Sequence Database (RefSeq). These sequences represent the protein coding region of the FAM47E-STBD1 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)	Select
OHu00868	NM_001242939.1 Latest version!	Homo sapiens FAM47E-STBD1 readthrough (FAM47E-STBD1), mRNA.	pcDNA3.1-C-(k)DYK or customized vector	7-9	$223.30 $319.00

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** 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.

Reference Sequences (Refseq)

FAM47E-STBD1 ( NM_001242939.1 ) cDNA ORF clone, Homo sapiens(human) -> NP_001229868.1 Homo sapiens FAM47E-STBD1 readthrough (FAM47E-STBD1), mRNA.

Price & Availability↑

CloneID	OHu00868
Clone ID Related Accession (Same CDS sequence)	NM_001242939.1
Accession Version	NM_001242939.1 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	2019-03-18
Organism	Homo sapiens(human)
Product	uncharacterized protein LOC100631383
Comment	Comment: VALIDATED REFSEQ: This record has undergone validation or preliminary review. The reference sequence was derived from AC034139.7 and AK092277.1. Sequence Note: This RefSeq record was created from transcript and genomic sequence data to make the sequence consistent with the reference genome assembly. The genomic coordinates used for the transcript record were based on transcript alignments. ##Evidence-Data-START## Transcript exon combination :: AK092277.1 [ECO:0000332] RNAseq introns :: single sample supports all introns SAMEA2144120 [ECO:0000348] ##Evidence-Data-END## ##RefSeq-Attributes-START## readthrough transcript :: includes exons from GeneID 8987, 100129583 ##RefSeq-Attributes-END## COMPLETENESS: complete on the 3' end.

ATGGCGGACC GCAGGCGGCG GCTCCGGCCG GGGACGTTGG CCCCGGTGCG CGAGGGCGTG 
AACTGCAGGT CCAGATGTTT CACAAAGCAC AAGAACGGGC TGAAGTTCCC CACCTCTCTG 
CACAGCCGGC AGTTGGTATT TCCAAGAAAG GGGCTGGACG ACTTCAGGAA GGGCTGCCCG 
CCTTGCACTG GTCTGGTGAC TCAGGTCCCT GTGGAGGGCT TTCTGCCCCA GATTTATCAC 
AGAGCTCCCC AACTGGCCCC AAAGAAGAGG CAGATCAAGC TGCTCAAGGA AGCAGACGTG 
CTTTCCAAGC TCTCGCCAGC CCAGCAGGCT CGGAAGGCAT TCCTGGAGGA CGTGGAGGCC 
CACCTGACCC CACATCCCTT AGCGCTCTAC CTGAATCTGG AAGAAGCTAT GCCCATAGAG 
CTCTTATCAA AGGTGCTGGA AGTGCTTGAT CCTGACCGGA AGCTGGAGGA CACATGGGCT 
TATTGTCAGG ACACCAGGAA AGGAATGAAG GAACCCACGA AGCTTTTAAA AAAACATTCT 
ACCCAAGTCT ACCTGGGACC TTCCAAGAAG ACGTCTGTGT CAAACGCAGG CCAATGGCTT 
TATGAAGAAA AGCCACATAA AATGGATTTG CTCCATGAAA ATGGTCCTCG TCCTGGTCTT 
CATGAAAATG GAATTTCGGA CATCGATGAA GAGTTCATCT TGAAACAGTT TGACATTGAC 
TATGAGACCA AACCAAGCCA TGATGCGCTC CACACGATGA AGCTAAATCA GGTTCCTCTG 
GAGCTAAAGC GTAGTGTGGG GCTCAGTAAA CTGCAGGAGA CAGAGTTCTT CCAGAAACTA 
GGCTATGAGA GGAAACTCCA GAAACCACAG AATCCTTATA AGCCAAAGTG GGTGAAGATG 
AGGTATGGAG CATGGTATTT GAACCCCAAG TTGTGGAAAA AGCAAAGAGT AGACGAGCCT 
CTGGTTGACC CTGAGGTCTC ACATAAGGCT CAAGAGGAGA ATTTTAAAAA GGAGCTGCAG 
GAACAGAGCA TCTTCAAGAA AGCAATGGAC ATTTGA

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

RefSeq	NP_001229868.1
CDS	48..1103
Translation	MADRRRRLRPGTLAPVREGVNCRSRCFTKHKNGLKFPTSLHSRQLVFPRKGLDDFRKGCPPCTGLVTQVPVEGFLPQIYHRAPQLAPKKRQIKLLKEADVLSKLSPAQQARKAFLEDVEAHLTPHPLALYLNLEEAMPIELLSKVLEVLDPDRKLEDTWAYCQDTRKGMKEPTKLLKKHSTQVYLGPSKKTSVSNAGQWLYEEKPHKMDLLHENGPRPGLHENGISDIDEEFILKQFDIDYETKPSHDALHTMKLNQVPLELKRSVGLSKLQETEFFQKLGYERKLQKPQNPYKPKWVKMRYGAWYLNPKLWKKQRVDEPLVDPEVSHKAQEENFKKELQEQSIFKKAMDI

Target ORF information:

RefSeq Version	NM_001242939.1
Organism	Homo sapiens(human)
Definition	Homo sapiens FAM47E-STBD1 readthrough (FAM47E-STBD1), mRNA.

Target ORF information:

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

NM_001242939.1

ORF Insert Sequence:

ATGGCGGACC GCAGGCGGCG GCTCCGGCCG GGGACGTTGG CCCCGGTGCG CGAGGGCGTG 
AACTGCAGGT CCAGATGTTT CACAAAGCAC AAGAACGGGC TGAAGTTCCC CACCTCTCTG 
CACAGCCGGC AGTTGGTATT TCCAAGAAAG GGGCTGGACG ACTTCAGGAA GGGCTGCCCG 
CCTTGCACTG GTCTGGTGAC TCAGGTCCCT GTGGAGGGCT TTCTGCCCCA GATTTATCAC 
AGAGCTCCCC AACTGGCCCC AAAGAAGAGG CAGATCAAGC TGCTCAAGGA AGCAGACGTG 
CTTTCCAAGC TCTCGCCAGC CCAGCAGGCT CGGAAGGCAT TCCTGGAGGA CGTGGAGGCC 
CACCTGACCC CACATCCCTT AGCGCTCTAC CTGAATCTGG AAGAAGCTAT GCCCATAGAG 
CTCTTATCAA AGGTGCTGGA AGTGCTTGAT CCTGACCGGA AGCTGGAGGA CACATGGGCT 
TATTGTCAGG ACACCAGGAA AGGAATGAAG GAACCCACGA AGCTTTTAAA AAAACATTCT 
ACCCAAGTCT ACCTGGGACC TTCCAAGAAG ACGTCTGTGT CAAACGCAGG CCAATGGCTT 
TATGAAGAAA AGCCACATAA AATGGATTTG CTCCATGAAA ATGGTCCTCG TCCTGGTCTT 
CATGAAAATG GAATTTCGGA CATCGATGAA GAGTTCATCT TGAAACAGTT TGACATTGAC 
TATGAGACCA AACCAAGCCA TGATGCGCTC CACACGATGA AGCTAAATCA GGTTCCTCTG 
GAGCTAAAGC GTAGTGTGGG GCTCAGTAAA CTGCAGGAGA CAGAGTTCTT CCAGAAACTA 
GGCTATGAGA GGAAACTCCA GAAACCACAG AATCCTTATA AGCCAAAGTG GGTGAAGATG 
AGGTATGGAG CATGGTATTT GAACCCCAAG TTGTGGAAAA AGCAAAGAGT AGACGAGCCT 
CTGGTTGACC CTGAGGTCTC ACATAAGGCT CAAGAGGAGA ATTTTAAAAA GGAGCTGCAG 
GAACAGAGCA TCTTCAAGAA AGCAATGGAC ATTTGA

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

PubMed

Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease.
Nature genetics46(9)989-93(2014 Sep)
Nalls MA,Pankratz N,Lill CM,Do CB,Hernandez DG,Saad M,DeStefano AL,Kara E,Bras J,Sharma M,Schulte C,Keller MF,Arepalli S,Letson C,Edsall C,Stefansson H,Liu X,Pliner H,Lee JH,Cheng R,,,,,,,,,,,,,Ikram MA,Ioannidis JP,Hadjigeorgiou GM,Bis JC,Martinez M,Perlmutter JS,Goate A,Marder K,Fiske B,Sutherland M,Xiromerisiou G,Myers RH,Clark LN,Stefansson K,Hardy JA,Heutink P,Chen H,Wood NW,Houlden H,Payami H,Brice A,Scott WK,Gasser T,Bertram L,Eriksson N,Foroud T,Singleton AB

Web-based genome-wide association study identifies two novel loci and a substantial genetic component for Parkinson's disease.
PLoS genetics7(6)e1002141(2011 Jun)
Do CB,Tung JY,Dorfman E,Kiefer AK,Drabant EM,Francke U,Mountain JL,Goldman SM,Tanner CM,Langston JW,Wojcicki A,Eriksson N

Expression of conjoined genes: another mechanism for gene regulation in eukaryotes.
PloS one5(10)e13284(2010 Oct)
Prakash T,Sharma VK,Adati N,Ozawa R,Kumar N,Nishida Y,Fujikake T,Takeda T,Taylor TD

Genome-wide association study reveals genetic risk underlying Parkinson's disease.
Nature genetics41(12)1308-12(2009 Dec)
Sim?n-S?nchez J,Schulte C,Bras JM,Sharma M,Gibbs JR,Berg D,Paisan-Ruiz C,Lichtner P,Scholz SW,Hernandez DG,Kr?ger R,Federoff M,Klein C,Goate A,Perlmutter J,Bonin M,Nalls MA,Illig T,Gieger C,Houlden H,Steffens M,Okun MS,Racette BA,Cookson MR,Foote KD,Fernandez HH,Traynor BJ,Schreiber S,Arepalli S,Zonozi R,Gwinn K,van der Brug M,Lopez G,Chanock SJ,Schatzkin A,Park Y,Hollenbeck A,Gao J,Huang X,Wood NW,Lorenz D,Deuschl G,Chen H,Riess O,Hardy JA,Singleton AB,Gasser T

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FAM47E-STBD1 cDNA ORF clone, Homo sapiens(human)

Gene

Clones

gRNAs

Related articles in PubMed

Target ORF information:

Target ORF information:

ORF Insert Sequence:

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