ODF3B cDNA ORF clone, Homo sapiens(human)

Gene
Clones
gRNAs

Summary

Gene Symbol	ODF3B
Entrez Gene ID	440836
Full Name	outer dense fiber of sperm tails 3B
Synonyms	ODF3L3
General protein information	Preferred Names outer dense fiber of sperm tails 3B Names outer dense fiber protein 3B orf2 5' to PD-ECGF/TP outer dense fiber protein 3-like protein 3
Gene Type	protein-coding
Organism	Homo sapiens(human)
Genome	Chromosome: 22 Map Location: 22q13.33

mRNA and Protein(s)

mRNA	Protein	Name
NM_001014440.3	NP_001014440.2	outer dense fiber protein 3B

Pathways from BioSystems

Homologies

Homo sapiens (human)	ODF3B	NP_001014440.2
	ODF3B	XP_001116356.1
Pan troglodytes (chimpanzee)	ODF3B	XP_003317369.1
Mus musculus (house mouse)	Odf3b	NP_001013040.1
Rattus norvegicus (Norway rat)	Odf3b	NP_001178921.1

Gene Ontology
Bibliography

Related articles in PubMed

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)

Seventy-five genetic loci influencing the human red blood cell.
van der Harst P, Zhang W, Mateo Leach I, Rendon A, Verweij N, Sehmi J, Paul DS, Elling U, Allayee H, Li X, Radhakrishnan A, Tan ST, Voss K, Weichenberger CX, Albers CA, Al-Hussani A, Asselbergs FW, Ciullo M, Danjou F, Dina C, Esko T, Evans DM, Franke L, G?gele M, Hartiala J, Hersch M, Holm H, Hottenga JJ, Kanoni S, Kleber ME, Lagou V, Langenberg C, Lopez LM, Lyytik?inen LP, Melander O, Murgia F, Nolte IM, O'Reilly PF, Padmanabhan S, Parsa A, Pirastu N, Porcu E, Portas L, Prokopenko I, Ried JS, Shin SY, Tang CS, Teumer A, Traglia M, Ulivi S, Westra HJ, Yang J, Zhao JH, Anni F, Abdellaoui A, Attwood A, Balkau B, Bandinelli S, Bastardot F, Benyamin B, Boehm BO, Cookson WO, Das D, de Bakker PI, de Boer RA, de Geus EJ, de Moor MH, Dimitriou M, Domingues FS, D?ring A, Engstr?m G, Eyjolfsson GI, Ferrucci L, Fischer K, Galanello R, Garner SF, Genser B, Gibson QD, Girotto G, Gudbjartsson DF, Harris SE, Hartikainen AL, Hastie CE, Hedblad B, Illig T, Jolley J, K?h?nen M, Kema IP, Kemp JP, Liang L, Lloyd-Jones H, Loos RJ, Meacham S, Medland SE, Meisinger C, Memari Y, Mihailov E, Miller K, Moffatt MF, Nauck M, Novatchkova M, Nutile T, Olafsson I, Onundarson PT, Parracciani D, Penninx BW, Perseu L, Piga A, Pistis G, Pouta A, Puc U, Raitakari O, Ring SM, Robino A, Ruggiero D, Ruokonen A, Saint-Pierre A, Sala C, Salumets A, Sambrook J, Schepers H, Schmidt CO, Sillj? HH, Sladek R, Smit JH, Starr JM, Stephens J, Sulem P, Tanaka T, Thorsteinsdottir U, Tragante V, van Gilst WH, van Pelt LJ, van Veldhuisen DJ, V?lker U, Whitfield JB, Willemsen G, Winkelmann BR, Wirnsberger G, Algra A, Cucca F, d'Adamo AP, Danesh J, Deary IJ, Dominiczak AF, Elliott P, Fortina P, Froguel P, Gasparini P, Greinacher A, Hazen SL, Jarvelin MR, Khaw KT, Lehtim?ki T, Maerz W, Martin NG, Metspalu A, Mitchell BD, Montgomery GW, Moore C, Navis G, Pirastu M, Pramstaller PP, Ramirez-Solis R, Schadt E, Scott J, Shuldiner AR, Smith GD, Smith JG, Snieder H, Sorice R, Spector TD, Stefansson K, Stumvoll M, Tang WH, Toniolo D, T?njes A, Visscher PM, Vollenweider P, Wareham NJ, Wolffenbuttel BH, Boomsma DI, Beckmann JS, Dedoussis GV, Deloukas P, Ferreira MA, Sanna S, Uda M, Hicks AA, Penninger JM, Gieger C, Kooner JS, Ouwehand WH, Soranzo N, Chambers JC
Nature492(7429)369-75(2012 Dec)

Novel genetic loci identified for the pathophysiology of childhood obesity in the Hispanic population.
Comuzzie AG, Cole SA, Laston SL, Voruganti VS, Haack K, Gibbs RA, Butte NF
PloS one7(12)e51954(2012)

Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.
, , Sawcer S, Hellenthal G, Pirinen M, Spencer CC, Patsopoulos NA, Moutsianas L, Dilthey A, Su Z, Freeman C, Hunt SE, Edkins S, Gray E, Booth DR, Potter SC, Goris A, Band G, Oturai AB, Strange A, Saarela J, Bellenguez C, Fontaine B, Gillman M, Hemmer B, Gwilliam R, Zipp F, Jayakumar A, Martin R, Leslie S, Hawkins S, Giannoulatou E, D'alfonso S, Blackburn H, Martinelli Boneschi F, Liddle J, Harbo HF, Perez ML, Spurkland A, Waller MJ, Mycko MP, Ricketts M, Comabella M, Hammond N, Kockum I, McCann OT, Ban M, Whittaker P, Kemppinen A, Weston P, Hawkins C, Widaa S, Zajicek J, Dronov S, Robertson N, Bumpstead SJ, Barcellos LF, Ravindrarajah R, Abraham R, Alfredsson L, Ardlie K, Aubin C, Baker A, Baker K, Baranzini SE, Bergamaschi L, Bergamaschi R, Bernstein A, Berthele A, Boggild M, Bradfield JP, Brassat D, Broadley SA, Buck D, Butzkueven H, Capra R, Carroll WM, Cavalla P, Celius EG, Cepok S, Chiavacci R, Clerget-Darpoux F, Clysters K, Comi G, Cossburn M, Cournu-Rebeix I, Cox MB, Cozen W, Cree BA, Cross AH, Cusi D, Daly MJ, Davis E, de Bakker PI, Debouverie M, D'hooghe MB, Dixon K, Dobosi R, Dubois B, Ellinghaus D, Elovaara I, Esposito F, Fontenille C, Foote S, Franke A, Galimberti D, Ghezzi A, Glessner J, Gomez R, Gout O, Graham C, Grant SF, Guerini FR, Hakonarson H, Hall P, Hamsten A, Hartung HP, Heard RN, Heath S, Hobart J, Hoshi M, Infante-Duarte C, Ingram G, Ingram W, Islam T, Jagodic M, Kabesch M, Kermode AG, Kilpatrick TJ, Kim C, Klopp N, Koivisto K, Larsson M, Lathrop M, Lechner-Scott JS, Leone MA, Lepp? V, Liljedahl U, Bomfim IL, Lincoln RR, Link J, Liu J, Lorentzen AR, Lupoli S, Macciardi F, Mack T, Marriott M, Martinelli V, Mason D, McCauley JL, Mentch F, Mero IL, Mihalova T, Montalban X, Mottershead J, Myhr KM, Naldi P, Ollier W, Page A, Palotie A, Pelletier J, Piccio L, Pickersgill T, Piehl F, Pobywajlo S, Quach HL, Ramsay PP, Reunanen M, Reynolds R, Rioux JD, Rodegher M, Roesner S, Rubio JP, R?ckert IM, Salvetti M, Salvi E, Santaniello A, Schaefer CA, Schreiber S, Schulze C, Scott RJ, Sellebjerg F, Selmaj KW, Sexton D, Shen L, Simms-Acuna B, Skidmore S, Sleiman PM, Smestad C, S?rensen PS, S?ndergaard HB, Stankovich J, Strange RC, Sulonen AM, Sundqvist E, Syv?nen AC, Taddeo F, Taylor B, Blackwell JM, Tienari P, Bramon E, Tourbah A, Brown MA, Tronczynska E, Casas JP, Tubridy N, Corvin A, Vickery J, Jankowski J, Villoslada P, Markus HS, Wang K, Mathew CG, Wason J, Palmer CN, Wichmann HE, Plomin R, Willoughby E, Rautanen A, Winkelmann J, Wittig M, Trembath RC, Yaouanq J, Viswanathan AC, Zhang H, Wood NW, Zuvich R, Deloukas P, Langford C, Duncanson A, Oksenberg JR, Pericak-Vance MA, Haines JL, Olsson T, Hillert J, Ivinson AJ, De Jager PL, Peltonen L, Stewart GJ, Hafler DA, Hauser SL, McVean G, Donnelly P, Compston A
Nature476(7359)214-9(2011 Aug)

Variation at the NFATC2 locus increases the risk of thiazolidinedione-induced edema in the Diabetes REduction Assessment with ramipril and rosiglitazone Medication (DREAM) study.
Bailey SD, Xie C, Do R, Montpetit A, Diaz R, Mohan V, Keavney B, Yusuf S, Gerstein HC, Engert JC, Anand S,
Diabetes care33(10)2250-3(2010 Oct)

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

Observational study of gene-disease association, gene-environment interaction, and pharmacogenomic / toxicogenomic. (HuGE Navigator)
Title: Variation at the NFATC2 locus increases the risk of thiazolidinedione-induced edema in the Diabetes REduction Assessment with ramipril and rosiglitazone Medication (DREAM) study.

Observational study of gene-disease association. (HuGE Navigator)
Title: Gene-centric association signals for lipids and apolipoproteins identified via the HumanCVD BeadChip.

The following ODF3B gene cDNA ORF clone sequences were retrieved from the NCBI Reference Sequence Database (RefSeq). These sequences represent the protein coding region of the ODF3B 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
OHu04148	NM_001014440.3 Latest version!	Homo sapiens outer dense fiber of sperm tails 3B (ODF3B), mRNA.	pcDNA3.1-C-(k)DYK or customized vector	in pcDNA3.1-C-(k)DYK	$99.50-$139.30 $199.00

ORF Online Only Promotion

Next-day Shipping ORF Clones ( in default vector with tag)
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*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.

Reference Sequences (Refseq)

ODF3B ( NM_001014440.3 ) cDNA ORF clone, Homo sapiens(human) -> NP_001014440.2 Homo sapiens outer dense fiber of sperm tails 3B (ODF3B), mRNA.

Price & Availability↑

CloneID	OHu04148
Clone ID Related Accession (Same CDS sequence)	NM_001014440.3
Accession Version	NM_001014440.3 Latest version!	Documents for ORF clone product in default vector
Sequence Information	ORF Nucleotide Sequence (Length: 762bp) 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	2019-08-03
Organism	Homo sapiens(human)
Product	outer dense fiber protein 3B
Comment	Comment: VALIDATED REFSEQ: This record has undergone validation or preliminary review. The reference sequence was derived from AW291097.1, BG149596.1 and BC127935.1. On Apr 14, 2009 this sequence version replaced NM_001014440.2. ##Evidence-Data-START## Transcript exon combination :: SRR1163658.216834.1 [ECO:0000332] RNAseq introns :: mixed/partial sample support SAMEA1965299, SAMEA1966682 [ECO:0000350] ##Evidence-Data-END## ##RefSeq-Attributes-START## RefSeq Select criteria :: based on single protein-coding transcript ##RefSeq-Attributes-END## COMPLETENESS: complete on the 3' end.

ATGGGCTCGG ACGCCTGGGT GGGCCTTTGG CGGCCACACC GGCCCCGCGG CCCCATCGCG 
GCGCACTACG GAGGCCCCGG GCCCAAATAC AAGCTGCCGC CCAACACCGG CTACGCCCTG 
CATGACCCGT CGCGGCCGCG CGCCCCCGCC TTCACCTTCG GCGCGCGCTT CCCCACGCAG 
CAGACGACGT GCGGCCCCGG GCCAGGCCAC CTGGTGCCCG CTCGCATGAC CGTGCGCGGC 
ACCGACGGCG CCCCCGCCTA CTCCATCTAC GGCCGCCCAC GCCGCTCAGC GCCCTTCCTC 
ACTCCGGGAC CTGGCAGGTA CTTCCCGGAG CGAGCGGGGA ACGCGACGTA CCCCAGTGCG 
CCTCGGCACA CCATTGCTCC CCGAAACTGG GGTGTCCAGG CGGAACAGCA GAGCCCAGGT 
CCCGCGGCCT ATACGGTGCC CTCGCTCTTG GGTCCGCGCG TCATCGGCAA AGTCTCCGCC 
CCAACTTGCT CCATCTACGG CCGCAGAGCG GCTGGCAGTT TCTTCGAGGA CCTCAGCAAG 
ACCCCGGGCC CCTGCGCCTA TCAGGTCGTG AGTCCAGGGG TCTACAAGTC CCGGGCCCCC 
CAGTTCACGA TTCTGGCGCG GACTTCGCTC CCCCAAGACA ACACTCGGAA GCCAGGGCCC 
GCGGCCTACA ACGTGGATCA GCACCGGAAG CCCCGCGGCT GGAGTTTCGG GATCCGGCAC 
TCGGACTACC TGGCCCCGCT GGTGACCGAC GCGGACAACT GA

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

RefSeq	NP_001014440.2
CDS	138..899
Translation	MGSDAWVGLWRPHRPRGPIAAHYGGPGPKYKLPPNTGYALHDPSRPRAPAFTFGARFPTQQTTCGPGPGHLVPARMTVRGTDGAPAYSIYGRPRRSAPFLTPGPGRYFPERAGNATYPSAPRHTIAPRNWGVQAEQQSPGPAAYTVPSLLGPRVIGKVSAPTCSIYGRRAAGSFFEDLSKTPGPCAYQVVSPGVYKSRAPQFTILARTSLPQDNTRKPGPAAYNVDQHRKPRGWSFGIRHSDYLAPLVTDADN

Target ORF information:

RefSeq Version	NM_001014440.3
Organism	Homo sapiens(human)
Definition	Homo sapiens outer dense fiber of sperm tails 3B (ODF3B), mRNA.

Target ORF information:

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

NM_001014440.3

ORF Insert Sequence:

ATGGGCTCGG ACGCCTGGGT GGGCCTTTGG CGGCCACACC GGCCCCGCGG CCCCATCGCG 
GCGCACTACG GAGGCCCCGG GCCCAAATAC AAGCTGCCGC CCAACACCGG CTACGCCCTG 
CATGACCCGT CGCGGCCGCG CGCCCCCGCC TTCACCTTCG GCGCGCGCTT CCCCACGCAG 
CAGACGACGT GCGGCCCCGG GCCAGGCCAC CTGGTGCCCG CTCGCATGAC CGTGCGCGGC 
ACCGACGGCG CCCCCGCCTA CTCCATCTAC GGCCGCCCAC GCCGCTCAGC GCCCTTCCTC 
ACTCCGGGAC CTGGCAGGTA CTTCCCGGAG CGAGCGGGGA ACGCGACGTA CCCCAGTGCG 
CCTCGGCACA CCATTGCTCC CCGAAACTGG GGTGTCCAGG CGGAACAGCA GAGCCCAGGT 
CCCGCGGCCT ATACGGTGCC CTCGCTCTTG GGTCCGCGCG TCATCGGCAA AGTCTCCGCC 
CCAACTTGCT CCATCTACGG CCGCAGAGCG GCTGGCAGTT TCTTCGAGGA CCTCAGCAAG 
ACCCCGGGCC CCTGCGCCTA TCAGGTCGTG AGTCCAGGGG TCTACAAGTC CCGGGCCCCC 
CAGTTCACGA TTCTGGCGCG GACTTCGCTC CCCCAAGACA ACACTCGGAA GCCAGGGCCC 
GCGGCCTACA ACGTGGATCA GCACCGGAAG CCCCGCGGCT GGAGTTTCGG GATCCGGCAC 
TCGGACTACC TGGCCCCGCT GGTGACCGAC GCGGACAACT GA

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

PubMed

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

Seventy-five genetic loci influencing the human red blood cell.
Nature492(7429)369-75(2012 Dec)
van der Harst P,Zhang W,Mateo Leach I,Rendon A,Verweij N,Sehmi J,Paul DS,Elling U,Allayee H,Li X,Radhakrishnan A,Tan ST,Voss K,Weichenberger CX,Albers CA,Al-Hussani A,Asselbergs FW,Ciullo M,Danjou F,Dina C,Esko T,Evans DM,Franke L,G?gele M,Hartiala J,Hersch M,Holm H,Hottenga JJ,Kanoni S,Kleber ME,Lagou V,Langenberg C,Lopez LM,Lyytik?inen LP,Melander O,Murgia F,Nolte IM,O'Reilly PF,Padmanabhan S,Parsa A,Pirastu N,Porcu E,Portas L,Prokopenko I,Ried JS,Shin SY,Tang CS,Teumer A,Traglia M,Ulivi S,Westra HJ,Yang J,Zhao JH,Anni F,Abdellaoui A,Attwood A,Balkau B,Bandinelli S,Bastardot F,Benyamin B,Boehm BO,Cookson WO,Das D,de Bakker PI,de Boer RA,de Geus EJ,de Moor MH,Dimitriou M,Domingues FS,D?ring A,Engstr?m G,Eyjolfsson GI,Ferrucci L,Fischer K,Galanello R,Garner SF,Genser B,Gibson QD,Girotto G,Gudbjartsson DF,Harris SE,Hartikainen AL,Hastie CE,Hedblad B,Illig T,Jolley J,K?h?nen M,Kema IP,Kemp JP,Liang L,Lloyd-Jones H,Loos RJ,Meacham S,Medland SE,Meisinger C,Memari Y,Mihailov E,Miller K,Moffatt MF,Nauck M,Novatchkova M,Nutile T,Olafsson I,Onundarson PT,Parracciani D,Penninx BW,Perseu L,Piga A,Pistis G,Pouta A,Puc U,Raitakari O,Ring SM,Robino A,Ruggiero D,Ruokonen A,Saint-Pierre A,Sala C,Salumets A,Sambrook J,Schepers H,Schmidt CO,Sillj? HH,Sladek R,Smit JH,Starr JM,Stephens J,Sulem P,Tanaka T,Thorsteinsdottir U,Tragante V,van Gilst WH,van Pelt LJ,van Veldhuisen DJ,V?lker U,Whitfield JB,Willemsen G,Winkelmann BR,Wirnsberger G,Algra A,Cucca F,d'Adamo AP,Danesh J,Deary IJ,Dominiczak AF,Elliott P,Fortina P,Froguel P,Gasparini P,Greinacher A,Hazen SL,Jarvelin MR,Khaw KT,Lehtim?ki T,Maerz W,Martin NG,Metspalu A,Mitchell BD,Montgomery GW,Moore C,Navis G,Pirastu M,Pramstaller PP,Ramirez-Solis R,Schadt E,Scott J,Shuldiner AR,Smith GD,Smith JG,Snieder H,Sorice R,Spector TD,Stefansson K,Stumvoll M,Tang WH,Toniolo D,T?njes A,Visscher PM,Vollenweider P,Wareham NJ,Wolffenbuttel BH,Boomsma DI,Beckmann JS,Dedoussis GV,Deloukas P,Ferreira MA,Sanna S,Uda M,Hicks AA,Penninger JM,Gieger C,Kooner JS,Ouwehand WH,Soranzo N,Chambers JC

Novel genetic loci identified for the pathophysiology of childhood obesity in the Hispanic population.
PloS one7(12)e51954(2012)
Comuzzie AG,Cole SA,Laston SL,Voruganti VS,Haack K,Gibbs RA,Butte NF

Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.
Nature476(7359)214-9(2011 Aug)
,,Sawcer S,Hellenthal G,Pirinen M,Spencer CC,Patsopoulos NA,Moutsianas L,Dilthey A,Su Z,Freeman C,Hunt SE,Edkins S,Gray E,Booth DR,Potter SC,Goris A,Band G,Oturai AB,Strange A,Saarela J,Bellenguez C,Fontaine B,Gillman M,Hemmer B,Gwilliam R,Zipp F,Jayakumar A,Martin R,Leslie S,Hawkins S,Giannoulatou E,D'alfonso S,Blackburn H,Martinelli Boneschi F,Liddle J,Harbo HF,Perez ML,Spurkland A,Waller MJ,Mycko MP,Ricketts M,Comabella M,Hammond N,Kockum I,McCann OT,Ban M,Whittaker P,Kemppinen A,Weston P,Hawkins C,Widaa S,Zajicek J,Dronov S,Robertson N,Bumpstead SJ,Barcellos LF,Ravindrarajah R,Abraham R,Alfredsson L,Ardlie K,Aubin C,Baker A,Baker K,Baranzini SE,Bergamaschi L,Bergamaschi R,Bernstein A,Berthele A,Boggild M,Bradfield JP,Brassat D,Broadley SA,Buck D,Butzkueven H,Capra R,Carroll WM,Cavalla P,Celius EG,Cepok S,Chiavacci R,Clerget-Darpoux F,Clysters K,Comi G,Cossburn M,Cournu-Rebeix I,Cox MB,Cozen W,Cree BA,Cross AH,Cusi D,Daly MJ,Davis E,de Bakker PI,Debouverie M,D'hooghe MB,Dixon K,Dobosi R,Dubois B,Ellinghaus D,Elovaara I,Esposito F,Fontenille C,Foote S,Franke A,Galimberti D,Ghezzi A,Glessner J,Gomez R,Gout O,Graham C,Grant SF,Guerini FR,Hakonarson H,Hall P,Hamsten A,Hartung HP,Heard RN,Heath S,Hobart J,Hoshi M,Infante-Duarte C,Ingram G,Ingram W,Islam T,Jagodic M,Kabesch M,Kermode AG,Kilpatrick TJ,Kim C,Klopp N,Koivisto K,Larsson M,Lathrop M,Lechner-Scott JS,Leone MA,Lepp? V,Liljedahl U,Bomfim IL,Lincoln RR,Link J,Liu J,Lorentzen AR,Lupoli S,Macciardi F,Mack T,Marriott M,Martinelli V,Mason D,McCauley JL,Mentch F,Mero IL,Mihalova T,Montalban X,Mottershead J,Myhr KM,Naldi P,Ollier W,Page A,Palotie A,Pelletier J,Piccio L,Pickersgill T,Piehl F,Pobywajlo S,Quach HL,Ramsay PP,Reunanen M,Reynolds R,Rioux JD,Rodegher M,Roesner S,Rubio JP,R?ckert IM,Salvetti M,Salvi E,Santaniello A,Schaefer CA,Schreiber S,Schulze C,Scott RJ,Sellebjerg F,Selmaj KW,Sexton D,Shen L,Simms-Acuna B,Skidmore S,Sleiman PM,Smestad C,S?rensen PS,S?ndergaard HB,Stankovich J,Strange RC,Sulonen AM,Sundqvist E,Syv?nen AC,Taddeo F,Taylor B,Blackwell JM,Tienari P,Bramon E,Tourbah A,Brown MA,Tronczynska E,Casas JP,Tubridy N,Corvin A,Vickery J,Jankowski J,Villoslada P,Markus HS,Wang K,Mathew CG,Wason J,Palmer CN,Wichmann HE,Plomin R,Willoughby E,Rautanen A,Winkelmann J,Wittig M,Trembath RC,Yaouanq J,Viswanathan AC,Zhang H,Wood NW,Zuvich R,Deloukas P,Langford C,Duncanson A,Oksenberg JR,Pericak-Vance MA,Haines JL,Olsson T,Hillert J,Ivinson AJ,De Jager PL,Peltonen L,Stewart GJ,Hafler DA,Hauser SL,McVean G,Donnelly P,Compston A

Variation at the NFATC2 locus increases the risk of thiazolidinedione-induced edema in the Diabetes REduction Assessment with ramipril and rosiglitazone Medication (DREAM) study.
Diabetes care33(10)2250-3(2010 Oct)
Bailey SD,Xie C,Do R,Montpetit A,Diaz R,Mohan V,Keavney B,Yusuf S,Gerstein HC,Engert JC,Anand S,