SLC17A3 cDNA ORF clone, Homo sapiens(human)

Gene
Clones
gRNAs

Summary

Gene Symbol	SLC17A3
Entrez Gene ID	10786
Full Name	solute carrier family 17 member 3
Synonyms	GOUT4,NPT4,UAQTL4
General protein information	Preferred Names solute carrier family 17 member 3 Names sodium-dependent phosphate transport protein 4 Na(+)/PI cotransporter 4 sodium/phosphate cotransporter 4 solute carrier family 17 (organic anion transporter), member 3 solute carrier family 17 (sodium phosphate), member 3
Gene Type	protein-coding
Organism	Homo sapiens(human)
Genome	Chromosome: 6 Map Location: 6p22.2
Summary	The protein encoded by this gene is a voltage-driven transporter that excretes intracellular urate and organic anions from the blood into renal tubule cells. Two transcript variants encoding different isoforms have been found for this gene. The longer isoform is a plasma membrane protein with transporter activity while the shorter isoform localizes to the endoplasmic reticulum. [provided by RefSeq, Aug 2012].
Disorder MIM:	611034
Disorder Html:	[Uric acid concentration, serum, QTL4], 612671 (3); {Gout susceptibility 4}, 612671 (3)

mRNA and Protein(s)

mRNA	Protein	Name
NM_001098486.1	NP_001091956.1	sodium-dependent phosphate transport protein 4 isoform a
NM_001098486.2	NP_001091956.1	sodium-dependent phosphate transport protein 4 isoform a
NM_006632.4	NP_006623.2	sodium-dependent phosphate transport protein 4 isoform b
NM_006632.3	NP_006623.2	sodium-dependent phosphate transport protein 4 isoform b

Pathways from BioSystems

Homologies

Homo sapiens (human)	SLC17A3	NP_001091956.1
	SLC17A3	XP_001083774.1
Canis lupus familiaris (dog)	LOC478741	XP_535908.2
Mus musculus (house mouse)	Slc17a3	NP_598830.2
Pan troglodytes (chimpanzee)	SLC17A3	XP_518284.2
Bos taurus (cattle)	SLC17A3	NP_001069255.1
Rattus norvegicus (Norway rat)	Slc17a3	NP_705886.1

Gene Ontology
Bibliography

Related articles in PubMed

The homocysteine associated variant rs548987 of SLC17A3 confers susceptibility to ischemic stroke in Chinese population.
Huang S, Yin L, Xu Y, Zou C, Chen L
Journal of the neurological sciences37078-81(2016 Nov)

Gene-age interactions in blood pressure regulation: a large-scale investigation with the CHARGE, Global BPgen, and ICBP Consortia.
Simino J, Shi G, Bis JC, Chasman DI, Ehret GB, Gu X, Guo X, Hwang SJ, Sijbrands E, Smith AV, Verwoert GC, Bragg-Gresham JL, Cadby G, Chen P, Cheng CY, Corre T, de Boer RA, Goel A, Johnson T, Khor CC, , Llu?s-Ganella C, Luan J, Lyytik?inen LP, Nolte IM, Sim X, S?ber S, van der Most PJ, Verweij N, Zhao JH, Amin N, Boerwinkle E, Bouchard C, Dehghan A, Eiriksdottir G, Elosua R, Franco OH, Gieger C, Harris TB, Hercberg S, Hofman A, James AL, Johnson AD, K?h?nen M, Khaw KT, Kutalik Z, Larson MG, Launer LJ, Li G, Liu J, Liu K, Morrison AC, Navis G, Ong RT, Papanicolau GJ, Penninx BW, Psaty BM, Raffel LJ, Raitakari OT, Rice K, Rivadeneira F, Rose LM, Sanna S, Scott RA, Siscovick DS, Stolk RP, Uitterlinden AG, Vaidya D, van der Klauw MM, Vasan RS, Vithana EN, V?lker U, V?lzke H, Watkins H, Young TL, Aung T, Bochud M, Farrall M, Hartman CA, Laan M, Lakatta EG, Lehtim?ki T, Loos RJ, Lucas G, Meneton P, Palmer LJ, Rettig R, Snieder H, Tai ES, Teo YY, van der Harst P, Wareham NJ, Wijmenga C, Wong TY, Fornage M, Gudnason V, Levy D, Palmas W, Ridker PM, Rotter JI, van Duijn CM, Witteman JC, Chakravarti A, Rao DC
American journal of human genetics95(1)24-38(2014 Jul)

An atlas of genetic influences on human blood metabolites.
Shin SY, Fauman EB, Petersen AK, Krumsiek J, Santos R, Huang J, Arnold M, Erte I, Forgetta V, Yang TP, Walter K, Menni C, Chen L, Vasquez L, Valdes AM, Hyde CL, Wang V, Ziemek D, Roberts P, Xi L, Grundberg E, , Waldenberger M, Richards JB, Mohney RP, Milburn MV, John SL, Trimmer J, Theis FJ, Overington JP, Suhre K, Brosnan MJ, Gieger C, Kastenm?ller G, Spector TD, Soranzo N
Nature genetics46(6)543-550(2014 Jun)

Common genetic loci influencing plasma homocysteine concentrations and their effect on risk of coronary artery disease.
van Meurs JB, Pare G, Schwartz SM, Hazra A, Tanaka T, Vermeulen SH, Cotlarciuc I, Yuan X, M?larstig A, Bandinelli S, Bis JC, Blom H, Brown MJ, Chen C, Chen YD, Clarke RJ, Dehghan A, Erdmann J, Ferrucci L, Hamsten A, Hofman A, Hunter DJ, Goel A, Johnson AD, Kathiresan S, Kampman E, Kiel DP, Kiemeney LA, Chambers JC, Kraft P, Lindemans J, McKnight B, Nelson CP, O'Donnell CJ, Psaty BM, Ridker PM, Rivadeneira F, Rose LM, Seedorf U, Siscovick DS, Schunkert H, Selhub J, Ueland PM, Vollenweider P, Waeber G, Waterworth DM, Watkins H, Witteman JC, den Heijer M, Jacques P, Uitterlinden AG, Kooner JS, Rader DJ, Reilly MP, Mooser V, Chasman DI, Samani NJ, Ahmadi KR
The American journal of clinical nutrition98(3)668-76(2013 Sep)

Genome-wide association analyses identify 18 new loci associated with serum urate concentrations.
K?ttgen A, Albrecht E, Teumer A, Vitart V, Krumsiek J, Hundertmark C, Pistis G, Ruggiero D, O'Seaghdha CM, Haller T, Yang Q, Tanaka T, Johnson AD, Kutalik Z, Smith AV, Shi J, Struchalin M, Middelberg RP, Brown MJ, Gaffo AL, Pirastu N, Li G, Hayward C, Zemunik T, Huffman J, Yengo L, Zhao JH, Demirkan A, Feitosa MF, Liu X, Malerba G, Lopez LM, van der Harst P, Li X, Kleber ME, Hicks AA, Nolte IM, Johansson A, Murgia F, Wild SH, Bakker SJ, Peden JF, Dehghan A, Steri M, Tenesa A, Lagou V, Salo P, Mangino M, Rose LM, Lehtim?ki T, Woodward OM, Okada Y, Tin A, M?ller C, Oldmeadow C, Putku M, Czamara D, Kraft P, Frogheri L, Thun GA, Grotevendt A, Gislason GK, Harris TB, Launer LJ, McArdle P, Shuldiner AR, Boerwinkle E, Coresh J, Schmidt H, Schallert M, Martin NG, Montgomery GW, Kubo M, Nakamura Y, Tanaka T, Munroe PB, Samani NJ, Jacobs DR Jr, Liu K, D'Adamo P, Ulivi S, Rotter JI, Psaty BM, Vollenweider P, Waeber G, Campbell S, Devuyst O, Navarro P, Kolcic I, Hastie N, Balkau B, Froguel P, Esko T, Salumets A, Khaw KT, Langenberg C, Wareham NJ, Isaacs A, Kraja A, Zhang Q, Wild PS, Scott RJ, Holliday EG, Org E, Viigimaa M, Bandinelli S, Metter JE, Lupo A, Trabetti E, Sorice R, D?ring A, Lattka E, Strauch K, Theis F, Waldenberger M, Wichmann HE, Davies G, Gow AJ, Bruinenberg M, , Stolk RP, Kooner JS, Zhang W, Winkelmann BR, Boehm BO, Lucae S, Penninx BW, Smit JH, Curhan G, Mudgal P, Plenge RM, Portas L, Persico I, Kirin M, Wilson JF, Mateo Leach I, van Gilst WH, Goel A, Ongen H, Hofman A, Rivadeneira F, Uitterlinden AG, Imboden M, von Eckardstein A, Cucca F, Nagaraja R, Piras MG, Nauck M, Schurmann C, Budde K, Ernst F, Farrington SM, Theodoratou E, Prokopenko I, Stumvoll M, Jula A, Perola M, Salomaa V, Shin SY, Spector TD, Sala C, Ridker PM, K?h?nen M, Viikari J, Hengstenberg C, Nelson CP, , , , , Meschia JF, Nalls MA, Sharma P, Singleton AB, Kamatani N, Zeller T, Burnier M, Attia J, Laan M, Klopp N, Hillege HL, Kloiber S, Choi H, Pirastu M, Tore S, Probst-Hensch NM, V?lzke H, Gudnason V, Parsa A, Schmidt R, Whitfield JB, Fornage M, Gasparini P, Siscovick DS, Pola?ek O, Campbell H, Rudan I, Bouatia-Naji N, Metspalu A, Loos RJ, van Duijn CM, Borecki IB, Ferrucci L, Gambaro G, Deary IJ, Wolffenbuttel BH, Chambers JC, M?rz W, Pramstaller PP, Snieder H, Gyllensten U, Wright AF, Navis G, Watkins H, Witteman JC, Sanna S, Schipf S, Dunlop MG, T?njes A, Ripatti S, Soranzo N, Toniolo D, Chasman DI, Raitakari O, Kao WH, Ciullo M, Fox CS, Caulfield M, Bochud M, Gieger C
Nature genetics45(2)145-54(2013 Feb)

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

Study used rs548987 of SLC17A3 as a candidate variant of ischemic stroke and performed association analysis in a Chinese population; although rs548987 failed to show significant association with total ischemic stroke and large vessel disease subtype, the C allele of rs548987 showed significant association with small vessel disease subtype of ischemic stroke (OR=0.68, p=0.004).
Title: The homocysteine associated variant rs548987 of SLC17A3 confers susceptibility to ischemic stroke in Chinese population.

variants carrying SNP V257F, G279R, or P378L exhibited reduced transport of para-aminohippurate, bumetanide, estrone and urate; SNPs may contribute to inter-individual differences in disposition of anionic drugs and certain endogenous organic anions
Title: Functional analysis of human sodium-phosphate transporter 4 (NPT4/SLC17A3) polymorphisms.

hNPT4 (SLC17A3) mediated time- and concentration-dependent uptake of OTxA (K(m): 802.8 microM) in a pH- and voltage-sensitive manner.
Title: A novel human organic anion transporter NPT4 mediates the transport of ochratoxin A.

a model of urate secretion in the renal tubular cell, where intracellular urate taken up via OAT1 and/or OAT3 from the blood exits from the cell into the lumen via hNPT4.
Title: Human sodium phosphate transporter 4 (hNPT4/SLC17A3) as a common renal secretory pathway for drugs and urate.

Observational study of gene-disease association. (HuGE Navigator)
Title: Examination of genetic polymorphisms in newborns for signatures of sex-specific prenatal selection.

The following SLC17A3 gene cDNA ORF clone sequences were retrieved from the NCBI Reference Sequence Database (RefSeq). These sequences represent the protein coding region of the SLC17A3 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)
OHu17779	NM_001098486.2 Latest version!	Homo sapiens solute carrier family 17 member 3 (SLC17A3), transcript variant 1, mRNA.	pcDNA3.1-C-(k)DYK or customized vector	7-9	$293.30 $419.00
OHu30846	NM_006632.4 Latest version!	Homo sapiens solute carrier family 17 member 3 (SLC17A3), transcript variant 2, mRNA.	pcDNA3.1-C-(k)DYK or customized vector	7-9	$223.30 $319.00
View Old Accession Versions >>
OHu17779	NM_001098486.1	Homo sapiens solute carrier family 17 member 3 (SLC17A3), transcript variant 1, mRNA.	pcDNA3.1-C-(k)DYK or customized vector	7-9	$293.30 $419.00
OHu30846	NM_006632.3	Homo sapiens solute carrier family 17 member 3 (SLC17A3), 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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***One clone ID might be correlated to multiple accession numbers, which share the same CDS sequence.

Reference Sequences (Refseq)

SLC17A3 ( NM_001098486.1 ) cDNA ORF clone, Homo sapiens(human) -> NP_001091956.1 Homo sapiens solute carrier family 17 member 3 (SLC17A3), transcript variant 1, mRNA.

Price & Availability↑

CloneID	OHu17779
Clone ID Related Accession (Same CDS sequence)	NM_001098486.1 , NM_001098486.2
Accession Version	NM_001098486.1	Documents for ORF clone product in default vector
Sequence Information	ORF Nucleotide Sequence (Length: 1497bp) 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	2018-06-22
Organism	Homo sapiens(human)
Product	sodium-dependent phosphate transport protein 4 isoform a
Comment	Comment: REVIEWED REFSEQ: This record has been curated by NCBI staff. The reference sequence was derived from DC361549.1, DC340735.1, Z83953.1, CB163247.1, AL138726.12 and BX107915.1. This sequence is a reference standard in the RefSeqGene project. Transcript Variant: This variant (1) represents the longer transcript and encodes the longer isoform (a). 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 :: AK298271.1 [ECO:0000332] RNAseq introns :: single sample supports all introns SAMEA2159080 [ECO:0000348] ##Evidence-Data-END## COMPLETENESS: complete on the 3' end.

ATGGCCACCA AGACAGAGTT GAGTCCCACA GCAAGGGAGA GCAAGAACGC ACAAGATATG 
CAAGTGGATG AGACACTGAT CCCCAGGAAA GTTCCAAGTT TATGTTCTGC TCGCTATGGA 
ATAGCCCTCG TCTTACATTT CTGCAATTTC ACAACGATAG CACAAAATGT CATCATGAAC 
ATCACCATGG TAGCCATGGT CAACAGCACA AGCCCTCAAT CCCAGCTCAA TGATTCCTCT 
GAGGTGCTGC CTGTTGACTC ATTTGGTGGC CTAAGTAAAG CCCCAAAGAG TCTTCCTGCA 
AAGGCTCCTG TGTATGACTG GTCTCCTCAA ATCCAAGGCA TCATCTTTGG TGCTGTTGGC 
TATGGTGGCA TACTGACAAT GGCTCCCAGT GGATACCTGG CTGGAAGAGT AGGAACAAAG 
CGAGTGGTTG GCATTTCTTT GTTTGCAACT TCATTTCTCA CTCTATGCAT CCCTCTGGCC 
ACTGACTTTG GAATAGTCTT GCTCATTGTA ACTCGAATAG TCCAGGGCCT AAGCCAGTCC 
TCAATACTTG GGGGTCAGTT TGCAATTTGG GAAAAGTGGG GCCCTCCACA AGAACGAAGC 
AGACTCTGCA GCATTGCTTT ATCAGGAATG TTACTGGGAT GCTTTACTGC CATCCTCATA 
GGTGGCTTCA TTAGTGAAAC CCTTGGGTGG CCCTTTGTCT TCTATATCTT TGGAGGTGTT 
GGCTGTGTCT GCTGCCTTCT CTGGTTTGTT GTGATTTATG ATGACCCCGT TTCCTATCCA 
TGGATAAGCA CCTCAGAAAA AGAATACATC ATATCCTCCT TGAAACAACA GGTCGGGTCT 
TCTAAGCAGC CTCTTCCCAT CAAAGCTATG CTCAGATCTC TACCCATTTG GTCCATATGT 
TTAGGCTGTT TCAGCCATCA ATGGTTAGTT AGCACAATGG TTGTATACAT ACCAACTTAC 
ATCAGCTCTG TGTACCATGT TAACATCAGA GACAATGGAC TTCTATCTGC CCTTCCTTTT 
ATTGTTGCCT GGGTCATAGG CATGGTGGGA GGCTATCTGG CAGATTTCCT TCTAACCAAA 
AAGTTTAGAC TCATCACTGT GAGGAAAATT GCCACAATTT TAGGAAGTCT CCCCTCTTCA 
GCACTCATTG TGTCTCTGCC TTACCTCAAT TCCGGCTATA TCACAGCAAC TGCCTTGCTG 
ACGCTCTCTT GCGGATTAAG CACATTGTGT CAGTCAGGGA TTTATATCAA TGTCTTAGAT 
ATTGCTCCAA GGTATTCCAG TTTTCTCATG GGAGCATCAA GAGGATTTTC GAGCATAGCA 
CCTGTCATTG TACCCACTGT CAGTGGATTT CTTCTTAGTC AGGACCCTGA GTTTGGGTGG 
AGGAATGTCT TCTTCTTGCT GTTTGCCGTT AACCTGTTAG GACTACTCTT CTACCTCATA 
TTTGGAGAAG CAGATGTCCA AGAATGGGCT AAAGAGAGAA AACTCACTCG TTTATGA

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

RefSeq	NP_001091956.1
CDS	111..1607
Translation	MATKTELSPTARESKNAQDMQVDETLIPRKVPSLCSARYGIALVLHFCNFTTIAQNVIMNITMVAMVNSTSPQSQLNDSSEVLPVDSFGGLSKAPKSLPAKAPVYDWSPQIQGIIFGAVGYGGILTMAPSGYLAGRVGTKRVVGISLFATSFLTLCIPLATDFGIVLLIVTRIVQGLSQSSILGGQFAIWEKWGPPQERSRLCSIALSGMLLGCFTAILIGGFISETLGWPFVFYIFGGVGCVCCLLWFVVIYDDPVSYPWISTSEKEYIISSLKQQVGSSKQPLPIKAMLRSLPIWSICLGCFSHQWLVSTMVVYIPTYISSVYHVNIRDNGLLSALPFIVAWVIGMVGGYLADFLLTKKFRLITVRKIATILGSLPSSALIVSLPYLNSGYITATALLTLSCGLSTLCQSGIYINVLDIAPRYSSFLMGASRGFSSIAPVIVPTVSGFLLSQDPEFGWRNVFFLLFAVNLLGLLFYLIFGEADVQEWAKERKLTRL

Target ORF information:

RefSeq Version	NM_001098486.1
Organism	Homo sapiens(human)
Definition	Homo sapiens solute carrier family 17 member 3 (SLC17A3), transcript variant 1, mRNA.

Target ORF information:

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

NM_001098486.1

ORF Insert Sequence:

ATGGCCACCA AGACAGAGTT GAGTCCCACA GCAAGGGAGA GCAAGAACGC ACAAGATATG 
CAAGTGGATG AGACACTGAT CCCCAGGAAA GTTCCAAGTT TATGTTCTGC TCGCTATGGA 
ATAGCCCTCG TCTTACATTT CTGCAATTTC ACAACGATAG CACAAAATGT CATCATGAAC 
ATCACCATGG TAGCCATGGT CAACAGCACA AGCCCTCAAT CCCAGCTCAA TGATTCCTCT 
GAGGTGCTGC CTGTTGACTC ATTTGGTGGC CTAAGTAAAG CCCCAAAGAG TCTTCCTGCA 
AAGGCTCCTG TGTATGACTG GTCTCCTCAA ATCCAAGGCA TCATCTTTGG TGCTGTTGGC 
TATGGTGGCA TACTGACAAT GGCTCCCAGT GGATACCTGG CTGGAAGAGT AGGAACAAAG 
CGAGTGGTTG GCATTTCTTT GTTTGCAACT TCATTTCTCA CTCTATGCAT CCCTCTGGCC 
ACTGACTTTG GAATAGTCTT GCTCATTGTA ACTCGAATAG TCCAGGGCCT AAGCCAGTCC 
TCAATACTTG GGGGTCAGTT TGCAATTTGG GAAAAGTGGG GCCCTCCACA AGAACGAAGC 
AGACTCTGCA GCATTGCTTT ATCAGGAATG TTACTGGGAT GCTTTACTGC CATCCTCATA 
GGTGGCTTCA TTAGTGAAAC CCTTGGGTGG CCCTTTGTCT TCTATATCTT TGGAGGTGTT 
GGCTGTGTCT GCTGCCTTCT CTGGTTTGTT GTGATTTATG ATGACCCCGT TTCCTATCCA 
TGGATAAGCA CCTCAGAAAA AGAATACATC ATATCCTCCT TGAAACAACA GGTCGGGTCT 
TCTAAGCAGC CTCTTCCCAT CAAAGCTATG CTCAGATCTC TACCCATTTG GTCCATATGT 
TTAGGCTGTT TCAGCCATCA ATGGTTAGTT AGCACAATGG TTGTATACAT ACCAACTTAC 
ATCAGCTCTG TGTACCATGT TAACATCAGA GACAATGGAC TTCTATCTGC CCTTCCTTTT 
ATTGTTGCCT GGGTCATAGG CATGGTGGGA GGCTATCTGG CAGATTTCCT TCTAACCAAA 
AAGTTTAGAC TCATCACTGT GAGGAAAATT GCCACAATTT TAGGAAGTCT CCCCTCTTCA 
GCACTCATTG TGTCTCTGCC TTACCTCAAT TCCGGCTATA TCACAGCAAC TGCCTTGCTG 
ACGCTCTCTT GCGGATTAAG CACATTGTGT CAGTCAGGGA TTTATATCAA TGTCTTAGAT 
ATTGCTCCAA GGTATTCCAG TTTTCTCATG GGAGCATCAA GAGGATTTTC GAGCATAGCA 
CCTGTCATTG TACCCACTGT CAGTGGATTT CTTCTTAGTC AGGACCCTGA GTTTGGGTGG 
AGGAATGTCT TCTTCTTGCT GTTTGCCGTT AACCTGTTAG GACTACTCTT CTACCTCATA 
TTTGGAGAAG CAGATGTCCA AGAATGGGCT AAAGAGAGAA AACTCACTCG TTTATGA

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

SLC17A3 ( NM_001098486.2 ) cDNA ORF clone, Homo sapiens(human) -> NP_001091956.1 Homo sapiens solute carrier family 17 member 3 (SLC17A3), transcript variant 1, mRNA.

Price & Availability↑

CloneID	OHu17779
Clone ID Related Accession (Same CDS sequence)	NM_001098486.1 , NM_001098486.2
Accession Version	NM_001098486.2 Latest version!	Documents for ORF clone product in default vector
Sequence Information	ORF Nucleotide Sequence (Length: 1497bp) 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	2019-08-21
Organism	Homo sapiens(human)
Product	sodium-dependent phosphate transport protein 4 isoform a
Comment	Comment: REVIEWED REFSEQ: This record has been curated by NCBI staff. The reference sequence was derived from DC361549.1, DC340735.1, Z83953.1, CB163247.1, AL138726.12 and BX107915.1. This sequence is a reference standard in the RefSeqGene project. On May 17, 2019 this sequence version replaced NM_001098486.1. Transcript Variant: This variant (1) represents the longer transcript and encodes the longer isoform (a). 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 :: AK298271.1 [ECO:0000332] RNAseq introns :: single sample supports all introns SAMEA2159080 [ECO:0000348] ##Evidence-Data-END## ##RefSeq-Attributes-START## MANE Ensembl match :: ENST00000397060.8/ ENSP00000380250.4 RefSeq Select criteria :: based on conservation, expression, longest protein ##RefSeq-Attributes-END## COMPLETENESS: complete on the 3' end.

ATGGCCACCA AGACAGAGTT GAGTCCCACA GCAAGGGAGA GCAAGAACGC ACAAGATATG 
CAAGTGGATG AGACACTGAT CCCCAGGAAA GTTCCAAGTT TATGTTCTGC TCGCTATGGA 
ATAGCCCTCG TCTTACATTT CTGCAATTTC ACAACGATAG CACAAAATGT CATCATGAAC 
ATCACCATGG TAGCCATGGT CAACAGCACA AGCCCTCAAT CCCAGCTCAA TGATTCCTCT 
GAGGTGCTGC CTGTTGACTC ATTTGGTGGC CTAAGTAAAG CCCCAAAGAG TCTTCCTGCA 
AAGGCTCCTG TGTATGACTG GTCTCCTCAA ATCCAAGGCA TCATCTTTGG TGCTGTTGGC 
TATGGTGGCA TACTGACAAT GGCTCCCAGT GGATACCTGG CTGGAAGAGT AGGAACAAAG 
CGAGTGGTTG GCATTTCTTT GTTTGCAACT TCATTTCTCA CTCTATGCAT CCCTCTGGCC 
ACTGACTTTG GAATAGTCTT GCTCATTGTA ACTCGAATAG TCCAGGGCCT AAGCCAGTCC 
TCAATACTTG GGGGTCAGTT TGCAATTTGG GAAAAGTGGG GCCCTCCACA AGAACGAAGC 
AGACTCTGCA GCATTGCTTT ATCAGGAATG TTACTGGGAT GCTTTACTGC CATCCTCATA 
GGTGGCTTCA TTAGTGAAAC CCTTGGGTGG CCCTTTGTCT TCTATATCTT TGGAGGTGTT 
GGCTGTGTCT GCTGCCTTCT CTGGTTTGTT GTGATTTATG ATGACCCCGT TTCCTATCCA 
TGGATAAGCA CCTCAGAAAA AGAATACATC ATATCCTCCT TGAAACAACA GGTCGGGTCT 
TCTAAGCAGC CTCTTCCCAT CAAAGCTATG CTCAGATCTC TACCCATTTG GTCCATATGT 
TTAGGCTGTT TCAGCCATCA ATGGTTAGTT AGCACAATGG TTGTATACAT ACCAACTTAC 
ATCAGCTCTG TGTACCATGT TAACATCAGA GACAATGGAC TTCTATCTGC CCTTCCTTTT 
ATTGTTGCCT GGGTCATAGG CATGGTGGGA GGCTATCTGG CAGATTTCCT TCTAACCAAA 
AAGTTTAGAC TCATCACTGT GAGGAAAATT GCCACAATTT TAGGAAGTCT CCCCTCTTCA 
GCACTCATTG TGTCTCTGCC TTACCTCAAT TCCGGCTATA TCACAGCAAC TGCCTTGCTG 
ACGCTCTCTT GCGGATTAAG CACATTGTGT CAGTCAGGGA TTTATATCAA TGTCTTAGAT 
ATTGCTCCAA GGTATTCCAG TTTTCTCATG GGAGCATCAA GAGGATTTTC GAGCATAGCA 
CCTGTCATTG TACCCACTGT CAGTGGATTT CTTCTTAGTC AGGACCCTGA GTTTGGGTGG 
AGGAATGTCT TCTTCTTGCT GTTTGCCGTT AACCTGTTAG GACTACTCTT CTACCTCATA 
TTTGGAGAAG CAGATGTCCA AGAATGGGCT AAAGAGAGAA AACTCACTCG TTTATGA

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

RefSeq	NP_001091956.1
CDS	111..1607
Translation	MATKTELSPTARESKNAQDMQVDETLIPRKVPSLCSARYGIALVLHFCNFTTIAQNVIMNITMVAMVNSTSPQSQLNDSSEVLPVDSFGGLSKAPKSLPAKAPVYDWSPQIQGIIFGAVGYGGILTMAPSGYLAGRVGTKRVVGISLFATSFLTLCIPLATDFGIVLLIVTRIVQGLSQSSILGGQFAIWEKWGPPQERSRLCSIALSGMLLGCFTAILIGGFISETLGWPFVFYIFGGVGCVCCLLWFVVIYDDPVSYPWISTSEKEYIISSLKQQVGSSKQPLPIKAMLRSLPIWSICLGCFSHQWLVSTMVVYIPTYISSVYHVNIRDNGLLSALPFIVAWVIGMVGGYLADFLLTKKFRLITVRKIATILGSLPSSALIVSLPYLNSGYITATALLTLSCGLSTLCQSGIYINVLDIAPRYSSFLMGASRGFSSIAPVIVPTVSGFLLSQDPEFGWRNVFFLLFAVNLLGLLFYLIFGEADVQEWAKERKLTRL

Target ORF information:

RefSeq Version	NM_001098486.2
Organism	Homo sapiens(human)
Definition	Homo sapiens solute carrier family 17 member 3 (SLC17A3), transcript variant 1, mRNA.

Target ORF information:

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

NM_001098486.2

ORF Insert Sequence:

ATGGCCACCA AGACAGAGTT GAGTCCCACA GCAAGGGAGA GCAAGAACGC ACAAGATATG 
CAAGTGGATG AGACACTGAT CCCCAGGAAA GTTCCAAGTT TATGTTCTGC TCGCTATGGA 
ATAGCCCTCG TCTTACATTT CTGCAATTTC ACAACGATAG CACAAAATGT CATCATGAAC 
ATCACCATGG TAGCCATGGT CAACAGCACA AGCCCTCAAT CCCAGCTCAA TGATTCCTCT 
GAGGTGCTGC CTGTTGACTC ATTTGGTGGC CTAAGTAAAG CCCCAAAGAG TCTTCCTGCA 
AAGGCTCCTG TGTATGACTG GTCTCCTCAA ATCCAAGGCA TCATCTTTGG TGCTGTTGGC 
TATGGTGGCA TACTGACAAT GGCTCCCAGT GGATACCTGG CTGGAAGAGT AGGAACAAAG 
CGAGTGGTTG GCATTTCTTT GTTTGCAACT TCATTTCTCA CTCTATGCAT CCCTCTGGCC 
ACTGACTTTG GAATAGTCTT GCTCATTGTA ACTCGAATAG TCCAGGGCCT AAGCCAGTCC 
TCAATACTTG GGGGTCAGTT TGCAATTTGG GAAAAGTGGG GCCCTCCACA AGAACGAAGC 
AGACTCTGCA GCATTGCTTT ATCAGGAATG TTACTGGGAT GCTTTACTGC CATCCTCATA 
GGTGGCTTCA TTAGTGAAAC CCTTGGGTGG CCCTTTGTCT TCTATATCTT TGGAGGTGTT 
GGCTGTGTCT GCTGCCTTCT CTGGTTTGTT GTGATTTATG ATGACCCCGT TTCCTATCCA 
TGGATAAGCA CCTCAGAAAA AGAATACATC ATATCCTCCT TGAAACAACA GGTCGGGTCT 
TCTAAGCAGC CTCTTCCCAT CAAAGCTATG CTCAGATCTC TACCCATTTG GTCCATATGT 
TTAGGCTGTT TCAGCCATCA ATGGTTAGTT AGCACAATGG TTGTATACAT ACCAACTTAC 
ATCAGCTCTG TGTACCATGT TAACATCAGA GACAATGGAC TTCTATCTGC CCTTCCTTTT 
ATTGTTGCCT GGGTCATAGG CATGGTGGGA GGCTATCTGG CAGATTTCCT TCTAACCAAA 
AAGTTTAGAC TCATCACTGT GAGGAAAATT GCCACAATTT TAGGAAGTCT CCCCTCTTCA 
GCACTCATTG TGTCTCTGCC TTACCTCAAT TCCGGCTATA TCACAGCAAC TGCCTTGCTG 
ACGCTCTCTT GCGGATTAAG CACATTGTGT CAGTCAGGGA TTTATATCAA TGTCTTAGAT 
ATTGCTCCAA GGTATTCCAG TTTTCTCATG GGAGCATCAA GAGGATTTTC GAGCATAGCA 
CCTGTCATTG TACCCACTGT CAGTGGATTT CTTCTTAGTC AGGACCCTGA GTTTGGGTGG 
AGGAATGTCT TCTTCTTGCT GTTTGCCGTT AACCTGTTAG GACTACTCTT CTACCTCATA 
TTTGGAGAAG CAGATGTCCA AGAATGGGCT AAAGAGAGAA AACTCACTCG TTTATGA

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

SLC17A3 ( NM_006632.4 ) cDNA ORF clone, Homo sapiens(human) -> NP_006623.2 Homo sapiens solute carrier family 17 member 3 (SLC17A3), transcript variant 2, mRNA.

Price & Availability↑

CloneID	OHu30846
Clone ID Related Accession (Same CDS sequence)	NM_006632.4 , NM_006632.3
Accession Version	NM_006632.4 Latest version!	Documents for ORF clone product in default vector
Sequence Information	ORF Nucleotide Sequence (Length: 1263bp) 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	2019-06-08
Organism	Homo sapiens(human)
Product	sodium-dependent phosphate transport protein 4 isoform b
Comment	Comment: REVIEWED REFSEQ: This record has been curated by NCBI staff. The reference sequence was derived from DC361549.1, BC017952.1 and AL138726.12. On Jun 1, 2019 this sequence version replaced NM_006632.3. Transcript Variant: This variant (2) lacks an alternate in-frame exon in the 5' coding region, compared to variant 1, resulting in a shorter protein (isoform b), compared to isoform a. 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 :: BC017952.1, DRR138522.1533926.1 [ECO:0000332] RNAseq introns :: single sample supports all introns SAMEA2159080 [ECO:0000348] ##Evidence-Data-END## COMPLETENESS: complete on the 3' end.

ATGGCCACCA AGACAGAGTT GAGTCCCACA GCAAGGGAGA GCAAGAACGC ACAAGATATG 
CAAGTGGATG AGACACTGAT CCCCAGGAAA GTTCCAAGTT TATGTTCTGC TCGCTATGGA 
ATAGCCCTCG TCTTACATTT CTGCAATTTC ACAACGATAG CACAAAATGT CATCATGAAC 
ATCACCATGG TAGCCATGGT CAACAGCACA AGCCCTCAAT CCCAGCTCAA TGATTCCTCT 
GAGGTGCTGC CTGTTGACTC ATTTGGTGGC CTAAGTAAAG CCCCAAAGAG TCTTCCTGCA 
AAGTCCTCAA TACTTGGGGG TCAGTTTGCA ATTTGGGAAA AGTGGGGCCC TCCACAAGAA 
CGAAGCAGAC TCTGCAGCAT TGCTTTATCA GGAATGTTAC TGGGATGCTT TACTGCCATC 
CTCATAGGTG GCTTCATTAG TGAAACCCTT GGGTGGCCCT TTGTCTTCTA TATCTTTGGA 
GGTGTTGGCT GTGTCTGCTG CCTTCTCTGG TTTGTTGTGA TTTATGATGA CCCCGTTTCC 
TATCCATGGA TAAGCACCTC AGAAAAAGAA TACATCATAT CCTCCTTGAA ACAACAGGTC 
GGGTCTTCTA AGCAGCCTCT TCCCATCAAA GCTATGCTCA GATCTCTACC CATTTGGTCC 
ATATGTTTAG GCTGTTTCAG CCATCAATGG TTAGTTAGCA CAATGGTTGT ATACATACCA 
ACTTACATCA GCTCTGTGTA CCATGTTAAC ATCAGAGACA ATGGACTTCT ATCTGCCCTT 
CCTTTTATTG TTGCCTGGGT CATAGGCATG GTGGGAGGCT ATCTGGCAGA TTTCCTTCTA 
ACCAAAAAGT TTAGACTCAT CACTGTGAGG AAAATTGCCA CAATTTTAGG AAGTCTCCCC 
TCTTCAGCAC TCATTGTGTC TCTGCCTTAC CTCAATTCCG GCTATATCAC AGCAACTGCC 
TTGCTGACGC TCTCTTGCGG ATTAAGCACA TTGTGTCAGT CAGGGATTTA TATCAATGTC 
TTAGATATTG CTCCAAGGTA TTCCAGTTTT CTCATGGGAG CATCAAGAGG ATTTTCGAGC 
ATAGCACCTG TCATTGTACC CACTGTCAGT GGATTTCTTC TTAGTCAGGA CCCTGAGTTT 
GGGTGGAGGA ATGTCTTCTT CTTGCTGTTT GCCGTTAACC TGTTAGGACT ACTCTTCTAC 
CTCATATTTG GAGAAGCAGA TGTCCAAGAA TGGGCTAAAG AGAGAAAACT CACTCGTTTA 
TGA

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

RefSeq	NP_006623.2
CDS	111..1373
Translation	MATKTELSPTARESKNAQDMQVDETLIPRKVPSLCSARYGIALVLHFCNFTTIAQNVIMNITMVAMVNSTSPQSQLNDSSEVLPVDSFGGLSKAPKSLPAKSSILGGQFAIWEKWGPPQERSRLCSIALSGMLLGCFTAILIGGFISETLGWPFVFYIFGGVGCVCCLLWFVVIYDDPVSYPWISTSEKEYIISSLKQQVGSSKQPLPIKAMLRSLPIWSICLGCFSHQWLVSTMVVYIPTYISSVYHVNIRDNGLLSALPFIVAWVIGMVGGYLADFLLTKKFRLITVRKIATILGSLPSSALIVSLPYLNSGYITATALLTLSCGLSTLCQSGIYINVLDIAPRYSSFLMGASRGFSSIAPVIVPTVSGFLLSQDPEFGWRNVFFLLFAVNLLGLLFYLIFGEADVQEWAKERKLTRL

Target ORF information:

RefSeq Version	NM_006632.4
Organism	Homo sapiens(human)
Definition	Homo sapiens solute carrier family 17 member 3 (SLC17A3), transcript variant 2, mRNA.

Target ORF information:

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

NM_006632.4

ORF Insert Sequence:

ATGGCCACCA AGACAGAGTT GAGTCCCACA GCAAGGGAGA GCAAGAACGC ACAAGATATG 
CAAGTGGATG AGACACTGAT CCCCAGGAAA GTTCCAAGTT TATGTTCTGC TCGCTATGGA 
ATAGCCCTCG TCTTACATTT CTGCAATTTC ACAACGATAG CACAAAATGT CATCATGAAC 
ATCACCATGG TAGCCATGGT CAACAGCACA AGCCCTCAAT CCCAGCTCAA TGATTCCTCT 
GAGGTGCTGC CTGTTGACTC ATTTGGTGGC CTAAGTAAAG CCCCAAAGAG TCTTCCTGCA 
AAGTCCTCAA TACTTGGGGG TCAGTTTGCA ATTTGGGAAA AGTGGGGCCC TCCACAAGAA 
CGAAGCAGAC TCTGCAGCAT TGCTTTATCA GGAATGTTAC TGGGATGCTT TACTGCCATC 
CTCATAGGTG GCTTCATTAG TGAAACCCTT GGGTGGCCCT TTGTCTTCTA TATCTTTGGA 
GGTGTTGGCT GTGTCTGCTG CCTTCTCTGG TTTGTTGTGA TTTATGATGA CCCCGTTTCC 
TATCCATGGA TAAGCACCTC AGAAAAAGAA TACATCATAT CCTCCTTGAA ACAACAGGTC 
GGGTCTTCTA AGCAGCCTCT TCCCATCAAA GCTATGCTCA GATCTCTACC CATTTGGTCC 
ATATGTTTAG GCTGTTTCAG CCATCAATGG TTAGTTAGCA CAATGGTTGT ATACATACCA 
ACTTACATCA GCTCTGTGTA CCATGTTAAC ATCAGAGACA ATGGACTTCT ATCTGCCCTT 
CCTTTTATTG TTGCCTGGGT CATAGGCATG GTGGGAGGCT ATCTGGCAGA TTTCCTTCTA 
ACCAAAAAGT TTAGACTCAT CACTGTGAGG AAAATTGCCA CAATTTTAGG AAGTCTCCCC 
TCTTCAGCAC TCATTGTGTC TCTGCCTTAC CTCAATTCCG GCTATATCAC AGCAACTGCC 
TTGCTGACGC TCTCTTGCGG ATTAAGCACA TTGTGTCAGT CAGGGATTTA TATCAATGTC 
TTAGATATTG CTCCAAGGTA TTCCAGTTTT CTCATGGGAG CATCAAGAGG ATTTTCGAGC 
ATAGCACCTG TCATTGTACC CACTGTCAGT GGATTTCTTC TTAGTCAGGA CCCTGAGTTT 
GGGTGGAGGA ATGTCTTCTT CTTGCTGTTT GCCGTTAACC TGTTAGGACT ACTCTTCTAC 
CTCATATTTG GAGAAGCAGA TGTCCAAGAA TGGGCTAAAG AGAGAAAACT CACTCGTTTA 
TGA

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

SLC17A3 ( NM_006632.3 ) cDNA ORF clone, Homo sapiens(human) -> NP_006623.2 Homo sapiens solute carrier family 17 member 3 (SLC17A3), transcript variant 2, mRNA.

Price & Availability↑

CloneID	OHu30846
Clone ID Related Accession (Same CDS sequence)	NM_006632.4 , NM_006632.3
Accession Version	NM_006632.3	Documents for ORF clone product in default vector
Sequence Information	ORF Nucleotide Sequence (Length: 1263bp) 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	2019-02-17
Organism	Homo sapiens(human)
Product	sodium-dependent phosphate transport protein 4 isoform b
Comment	Comment: REVIEWED REFSEQ: This record has been curated by NCBI staff. The reference sequence was derived from DC361549.1, BC017952.1 and AL138726.12. On Jun 8, 2007 this sequence version replaced NM_006632.2. Transcript Variant: This variant (2) lacks an alternate in-frame exon in the 5' coding region, compared to variant 1, resulting in a shorter protein (isoform b), compared to isoform a. 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 :: BC017952.1 [ECO:0000332] RNAseq introns :: single sample supports all introns SAMEA2159080 [ECO:0000348] ##Evidence-Data-END## COMPLETENESS: complete on the 3' end.

ATGGCCACCA AGACAGAGTT GAGTCCCACA GCAAGGGAGA GCAAGAACGC ACAAGATATG 
CAAGTGGATG AGACACTGAT CCCCAGGAAA GTTCCAAGTT TATGTTCTGC TCGCTATGGA 
ATAGCCCTCG TCTTACATTT CTGCAATTTC ACAACGATAG CACAAAATGT CATCATGAAC 
ATCACCATGG TAGCCATGGT CAACAGCACA AGCCCTCAAT CCCAGCTCAA TGATTCCTCT 
GAGGTGCTGC CTGTTGACTC ATTTGGTGGC CTAAGTAAAG CCCCAAAGAG TCTTCCTGCA 
AAGTCCTCAA TACTTGGGGG TCAGTTTGCA ATTTGGGAAA AGTGGGGCCC TCCACAAGAA 
CGAAGCAGAC TCTGCAGCAT TGCTTTATCA GGAATGTTAC TGGGATGCTT TACTGCCATC 
CTCATAGGTG GCTTCATTAG TGAAACCCTT GGGTGGCCCT TTGTCTTCTA TATCTTTGGA 
GGTGTTGGCT GTGTCTGCTG CCTTCTCTGG TTTGTTGTGA TTTATGATGA CCCCGTTTCC 
TATCCATGGA TAAGCACCTC AGAAAAAGAA TACATCATAT CCTCCTTGAA ACAACAGGTC 
GGGTCTTCTA AGCAGCCTCT TCCCATCAAA GCTATGCTCA GATCTCTACC CATTTGGTCC 
ATATGTTTAG GCTGTTTCAG CCATCAATGG TTAGTTAGCA CAATGGTTGT ATACATACCA 
ACTTACATCA GCTCTGTGTA CCATGTTAAC ATCAGAGACA ATGGACTTCT ATCTGCCCTT 
CCTTTTATTG TTGCCTGGGT CATAGGCATG GTGGGAGGCT ATCTGGCAGA TTTCCTTCTA 
ACCAAAAAGT TTAGACTCAT CACTGTGAGG AAAATTGCCA CAATTTTAGG AAGTCTCCCC 
TCTTCAGCAC TCATTGTGTC TCTGCCTTAC CTCAATTCCG GCTATATCAC AGCAACTGCC 
TTGCTGACGC TCTCTTGCGG ATTAAGCACA TTGTGTCAGT CAGGGATTTA TATCAATGTC 
TTAGATATTG CTCCAAGGTA TTCCAGTTTT CTCATGGGAG CATCAAGAGG ATTTTCGAGC 
ATAGCACCTG TCATTGTACC CACTGTCAGT GGATTTCTTC TTAGTCAGGA CCCTGAGTTT 
GGGTGGAGGA ATGTCTTCTT CTTGCTGTTT GCCGTTAACC TGTTAGGACT ACTCTTCTAC 
CTCATATTTG GAGAAGCAGA TGTCCAAGAA TGGGCTAAAG AGAGAAAACT CACTCGTTTA 
TGA

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

RefSeq	NP_006623.2
CDS	111..1373
Translation	MATKTELSPTARESKNAQDMQVDETLIPRKVPSLCSARYGIALVLHFCNFTTIAQNVIMNITMVAMVNSTSPQSQLNDSSEVLPVDSFGGLSKAPKSLPAKSSILGGQFAIWEKWGPPQERSRLCSIALSGMLLGCFTAILIGGFISETLGWPFVFYIFGGVGCVCCLLWFVVIYDDPVSYPWISTSEKEYIISSLKQQVGSSKQPLPIKAMLRSLPIWSICLGCFSHQWLVSTMVVYIPTYISSVYHVNIRDNGLLSALPFIVAWVIGMVGGYLADFLLTKKFRLITVRKIATILGSLPSSALIVSLPYLNSGYITATALLTLSCGLSTLCQSGIYINVLDIAPRYSSFLMGASRGFSSIAPVIVPTVSGFLLSQDPEFGWRNVFFLLFAVNLLGLLFYLIFGEADVQEWAKERKLTRL

Target ORF information:

RefSeq Version	NM_006632.3
Organism	Homo sapiens(human)
Definition	Homo sapiens solute carrier family 17 member 3 (SLC17A3), transcript variant 2, mRNA.

Target ORF information:

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

NM_006632.3

ORF Insert Sequence:

ATGGCCACCA AGACAGAGTT GAGTCCCACA GCAAGGGAGA GCAAGAACGC ACAAGATATG 
CAAGTGGATG AGACACTGAT CCCCAGGAAA GTTCCAAGTT TATGTTCTGC TCGCTATGGA 
ATAGCCCTCG TCTTACATTT CTGCAATTTC ACAACGATAG CACAAAATGT CATCATGAAC 
ATCACCATGG TAGCCATGGT CAACAGCACA AGCCCTCAAT CCCAGCTCAA TGATTCCTCT 
GAGGTGCTGC CTGTTGACTC ATTTGGTGGC CTAAGTAAAG CCCCAAAGAG TCTTCCTGCA 
AAGTCCTCAA TACTTGGGGG TCAGTTTGCA ATTTGGGAAA AGTGGGGCCC TCCACAAGAA 
CGAAGCAGAC TCTGCAGCAT TGCTTTATCA GGAATGTTAC TGGGATGCTT TACTGCCATC 
CTCATAGGTG GCTTCATTAG TGAAACCCTT GGGTGGCCCT TTGTCTTCTA TATCTTTGGA 
GGTGTTGGCT GTGTCTGCTG CCTTCTCTGG TTTGTTGTGA TTTATGATGA CCCCGTTTCC 
TATCCATGGA TAAGCACCTC AGAAAAAGAA TACATCATAT CCTCCTTGAA ACAACAGGTC 
GGGTCTTCTA AGCAGCCTCT TCCCATCAAA GCTATGCTCA GATCTCTACC CATTTGGTCC 
ATATGTTTAG GCTGTTTCAG CCATCAATGG TTAGTTAGCA CAATGGTTGT ATACATACCA 
ACTTACATCA GCTCTGTGTA CCATGTTAAC ATCAGAGACA ATGGACTTCT ATCTGCCCTT 
CCTTTTATTG TTGCCTGGGT CATAGGCATG GTGGGAGGCT ATCTGGCAGA TTTCCTTCTA 
ACCAAAAAGT TTAGACTCAT CACTGTGAGG AAAATTGCCA CAATTTTAGG AAGTCTCCCC 
TCTTCAGCAC TCATTGTGTC TCTGCCTTAC CTCAATTCCG GCTATATCAC AGCAACTGCC 
TTGCTGACGC TCTCTTGCGG ATTAAGCACA TTGTGTCAGT CAGGGATTTA TATCAATGTC 
TTAGATATTG CTCCAAGGTA TTCCAGTTTT CTCATGGGAG CATCAAGAGG ATTTTCGAGC 
ATAGCACCTG TCATTGTACC CACTGTCAGT GGATTTCTTC TTAGTCAGGA CCCTGAGTTT 
GGGTGGAGGA ATGTCTTCTT CTTGCTGTTT GCCGTTAACC TGTTAGGACT ACTCTTCTAC 
CTCATATTTG GAGAAGCAGA TGTCCAAGAA TGGGCTAAAG AGAGAAAACT CACTCGTTTA 
TGA

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

PubMed

The homocysteine associated variant rs548987 of SLC17A3 confers susceptibility to ischemic stroke in Chinese population.
Journal of the neurological sciences37078-81(2016 Nov)
Huang S,Yin L,Xu Y,Zou C,Chen L

Gene-age interactions in blood pressure regulation: a large-scale investigation with the CHARGE, Global BPgen, and ICBP Consortia.
American journal of human genetics95(1)24-38(2014 Jul)
Simino J,Shi G,Bis JC,Chasman DI,Ehret GB,Gu X,Guo X,Hwang SJ,Sijbrands E,Smith AV,Verwoert GC,Bragg-Gresham JL,Cadby G,Chen P,Cheng CY,Corre T,de Boer RA,Goel A,Johnson T,Khor CC,,Llu?s-Ganella C,Luan J,Lyytik?inen LP,Nolte IM,Sim X,S?ber S,van der Most PJ,Verweij N,Zhao JH,Amin N,Boerwinkle E,Bouchard C,Dehghan A,Eiriksdottir G,Elosua R,Franco OH,Gieger C,Harris TB,Hercberg S,Hofman A,James AL,Johnson AD,K?h?nen M,Khaw KT,Kutalik Z,Larson MG,Launer LJ,Li G,Liu J,Liu K,Morrison AC,Navis G,Ong RT,Papanicolau GJ,Penninx BW,Psaty BM,Raffel LJ,Raitakari OT,Rice K,Rivadeneira F,Rose LM,Sanna S,Scott RA,Siscovick DS,Stolk RP,Uitterlinden AG,Vaidya D,van der Klauw MM,Vasan RS,Vithana EN,V?lker U,V?lzke H,Watkins H,Young TL,Aung T,Bochud M,Farrall M,Hartman CA,Laan M,Lakatta EG,Lehtim?ki T,Loos RJ,Lucas G,Meneton P,Palmer LJ,Rettig R,Snieder H,Tai ES,Teo YY,van der Harst P,Wareham NJ,Wijmenga C,Wong TY,Fornage M,Gudnason V,Levy D,Palmas W,Ridker PM,Rotter JI,van Duijn CM,Witteman JC,Chakravarti A,Rao DC

An atlas of genetic influences on human blood metabolites.
Nature genetics46(6)543-550(2014 Jun)
Shin SY,Fauman EB,Petersen AK,Krumsiek J,Santos R,Huang J,Arnold M,Erte I,Forgetta V,Yang TP,Walter K,Menni C,Chen L,Vasquez L,Valdes AM,Hyde CL,Wang V,Ziemek D,Roberts P,Xi L,Grundberg E,,Waldenberger M,Richards JB,Mohney RP,Milburn MV,John SL,Trimmer J,Theis FJ,Overington JP,Suhre K,Brosnan MJ,Gieger C,Kastenm?ller G,Spector TD,Soranzo N

Common genetic loci influencing plasma homocysteine concentrations and their effect on risk of coronary artery disease.
The American journal of clinical nutrition98(3)668-76(2013 Sep)
van Meurs JB,Pare G,Schwartz SM,Hazra A,Tanaka T,Vermeulen SH,Cotlarciuc I,Yuan X,M?larstig A,Bandinelli S,Bis JC,Blom H,Brown MJ,Chen C,Chen YD,Clarke RJ,Dehghan A,Erdmann J,Ferrucci L,Hamsten A,Hofman A,Hunter DJ,Goel A,Johnson AD,Kathiresan S,Kampman E,Kiel DP,Kiemeney LA,Chambers JC,Kraft P,Lindemans J,McKnight B,Nelson CP,O'Donnell CJ,Psaty BM,Ridker PM,Rivadeneira F,Rose LM,Seedorf U,Siscovick DS,Schunkert H,Selhub J,Ueland PM,Vollenweider P,Waeber G,Waterworth DM,Watkins H,Witteman JC,den Heijer M,Jacques P,Uitterlinden AG,Kooner JS,Rader DJ,Reilly MP,Mooser V,Chasman DI,Samani NJ,Ahmadi KR

Genome-wide association analyses identify 18 new loci associated with serum urate concentrations.
Nature genetics45(2)145-54(2013 Feb)
K?ttgen A,Albrecht E,Teumer A,Vitart V,Krumsiek J,Hundertmark C,Pistis G,Ruggiero D,O'Seaghdha CM,Haller T,Yang Q,Tanaka T,Johnson AD,Kutalik Z,Smith AV,Shi J,Struchalin M,Middelberg RP,Brown MJ,Gaffo AL,Pirastu N,Li G,Hayward C,Zemunik T,Huffman J,Yengo L,Zhao JH,Demirkan A,Feitosa MF,Liu X,Malerba G,Lopez LM,van der Harst P,Li X,Kleber ME,Hicks AA,Nolte IM,Johansson A,Murgia F,Wild SH,Bakker SJ,Peden JF,Dehghan A,Steri M,Tenesa A,Lagou V,Salo P,Mangino M,Rose LM,Lehtim?ki T,Woodward OM,Okada Y,Tin A,M?ller C,Oldmeadow C,Putku M,Czamara D,Kraft P,Frogheri L,Thun GA,Grotevendt A,Gislason GK,Harris TB,Launer LJ,McArdle P,Shuldiner AR,Boerwinkle E,Coresh J,Schmidt H,Schallert M,Martin NG,Montgomery GW,Kubo M,Nakamura Y,Tanaka T,Munroe PB,Samani NJ,Jacobs DR Jr,Liu K,D'Adamo P,Ulivi S,Rotter JI,Psaty BM,Vollenweider P,Waeber G,Campbell S,Devuyst O,Navarro P,Kolcic I,Hastie N,Balkau B,Froguel P,Esko T,Salumets A,Khaw KT,Langenberg C,Wareham NJ,Isaacs A,Kraja A,Zhang Q,Wild PS,Scott RJ,Holliday EG,Org E,Viigimaa M,Bandinelli S,Metter JE,Lupo A,Trabetti E,Sorice R,D?ring A,Lattka E,Strauch K,Theis F,Waldenberger M,Wichmann HE,Davies G,Gow AJ,Bruinenberg M,,Stolk RP,Kooner JS,Zhang W,Winkelmann BR,Boehm BO,Lucae S,Penninx BW,Smit JH,Curhan G,Mudgal P,Plenge RM,Portas L,Persico I,Kirin M,Wilson JF,Mateo Leach I,van Gilst WH,Goel A,Ongen H,Hofman A,Rivadeneira F,Uitterlinden AG,Imboden M,von Eckardstein A,Cucca F,Nagaraja R,Piras MG,Nauck M,Schurmann C,Budde K,Ernst F,Farrington SM,Theodoratou E,Prokopenko I,Stumvoll M,Jula A,Perola M,Salomaa V,Shin SY,Spector TD,Sala C,Ridker PM,K?h?nen M,Viikari J,Hengstenberg C,Nelson CP,,,,,Meschia JF,Nalls MA,Sharma P,Singleton AB,Kamatani N,Zeller T,Burnier M,Attia J,Laan M,Klopp N,Hillege HL,Kloiber S,Choi H,Pirastu M,Tore S,Probst-Hensch NM,V?lzke H,Gudnason V,Parsa A,Schmidt R,Whitfield JB,Fornage M,Gasparini P,Siscovick DS,Pola?ek O,Campbell H,Rudan I,Bouatia-Naji N,Metspalu A,Loos RJ,van Duijn CM,Borecki IB,Ferrucci L,Gambaro G,Deary IJ,Wolffenbuttel BH,Chambers JC,M?rz W,Pramstaller PP,Snieder H,Gyllensten U,Wright AF,Navis G,Watkins H,Witteman JC,Sanna S,Schipf S,Dunlop MG,T?njes A,Ripatti S,Soranzo N,Toniolo D,Chasman DI,Raitakari O,Kao WH,Ciullo M,Fox CS,Caulfield M,Bochud M,Gieger C

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SLC17A3 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:

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