ORF » Species Summary » Homo sapiens » ARPIN-AP3S2 cDNA ORF clone

ARPIN-AP3S2 cDNA ORF clone, Homo sapiens(human)

  • Gene

  • Clones

  • gRNAs

The following ARPIN-AP3S2 gene cDNA ORF clone sequences were retrieved from the NCBI Reference Sequence Database (RefSeq). These sequences represent the protein coding region of the ARPIN-AP3S2 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
OHu12860 NM_001199058.2
Latest version!		 Homo sapiens ARPIN-AP3S2 readthrough (ARPIN-AP3S2), mRNA. pcDNA3.1-C-(k)DYK or customized vector 7-9 $230.30
$329.00
View Old Accession Versions >>
OHu12860 NM_001199058.1 Homo sapiens ARPIN-AP3S2 readthrough (ARPIN-AP3S2), mRNA. pcDNA3.1-C-(k)DYK or customized vector 7-9 $230.30
$329.00
Hide Old Accession Versions >>

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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)
    ARPIN-AP3S2 ( NM_001199058.1 ) cDNA ORF clone, Homo sapiens(human) -> NP_001185987.1 Homo sapiens ARPIN-AP3S2 readthrough (ARPIN-AP3S2), mRNA.
    Price & Availability↑
    CloneID OHu12860
    Clone ID Related Accession (Same CDS sequence) NM_001199058.1 , NM_001199058.2
    Accession Version NM_001199058.1 Documents for ORF clone product in default vector
    Sequence Information ORF Nucleotide Sequence (Length: 1185bp)
    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 2018-11-27
    Organism Homo sapiens(human)
    Product C15orf38-AP3S2 fusion protein
    Comment Comment: VALIDATED REFSEQ: This record has undergone validation or preliminary review. The reference sequence was derived from AC027176.23, AK000495.1 and AC018988.12. 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 :: SRR1803614.232486.1, SRR1803616.170778.1 [ECO:0000332] RNAseq introns :: mixed/partial sample support SAMEA1965299, SAMEA1966682 [ECO:0000350] ##Evidence-Data-END## ##RefSeq-Attributes-START## readthrough transcript :: includes exons from GeneID 10239, 348110 ##RefSeq-Attributes-END## COMPLETENESS: complete on the 3' end. 

    1
    61
    121
    181
    241
    301
    361
    421
    481
    541
    601
    661
    721
    781
    841
    901
    961
    1021
    1081
    1141
    ATGAGCCGCA TCTACCACGA CGGCGCGCTC CGGAACAAGG CGGTGCAGAG CGTCCGGCTG 
    CCAGGGGCCT GGGACCCCGC CGCCCACCAG GGGGGAAATG GTGTCCTGCT GGAGGGAGAA 
    CTGATCGATG TATCTCGGCA CAGCATCTTG GACACTCATG GCAGGAAGGA GCGCTACTAC 
    GTGCTGTATA TCCGGCCCAG TCACATCCAT CGCCGTAAAT TCGACGCCAA GGGAAATGAA 
    ATCGAGCCCA ACTTCAGCGC CACCAGGAAG GTGAACACGG GCTTCCTCAT GTCGTCCTAC 
    AAGGTGGAAG CCAAGGGGGA CACTGACAGG CTCACGCCCG AGGCGCTGAA GGGGCTGGTC 
    AACAAGCCAG AGCTGCTCGC GCTGACAGAG AGCCTCACCC CCGACCACAC AGTGGCGTTC 
    TGGATGCCCG AGTCAGAGAT GGAGGTGATG GAACTCGAGC TGGGGGCCGG GGTACGGCTG 
    AAGACTCGGG GCGATGGTCC CTTCCTGGAT TCATTGGCCA AACTTGAGGC TGGAACAGTG 
    ACCAAGTGTA ATTTCACTGG TGATGGAAAG ACAGGGGCAT CCTGGACAGA CAACATCATG 
    GCCCAAAAGT GTTCGAAGGG GGCTGCAGCG GAGATCCGAG AGCAGGGGGA TGGGGCAGAG 
    GACGAGGAGT GGCCAGAAGA AATTCAACAG CAGATTGTTC GAGAGACTTT CCATCTAGTC 
    CTCAAGCGGG ATGACAACAT CTGTAACTTC TTGGAGGGTG GAAGTTTGAT TGGTGGCTCT 
    GACTACAAAC TGATCTACCG GCACTATGCT ACCCTCTACT TTGTATTTTG TGTGGATTCC 
    TCAGAGAGTG AACTTGGAAT CTTGGACCTC ATCCAGGTTT TTGTGGAAAC TCTGGATAAG 
    TGTTTCGAAA ATGTGTGTGA ATTGGATTTG ATCTTCCATA TGGATAAGGT GCACTACATC 
    CTCCAGGAGG TGGTGATGGG TGGGATGGTG TTGGAAACAA ACATGAATGA AATCGTGGCT 
    CAGATTGAGG CTCAAAACAG GCTGGAGAAA TCCGAGGGTG GCCTTTCAGC AGCCCCTGCG 
    CGGGCTGTGT CTGCTGTGAA AAACATCAAC CTGCCAGAGA TTCCTCGGAA CATCAACATT 
    GGCGATCTCA ACATCAAAGT TCCCAACCTG TCCCAGTTTG TCTGA

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

    RefSeq NP_001185987.1
    CDS156..1340
    Translation

    Target ORF information:

    RefSeq Version NM_001199058.1
    Organism Homo sapiens(human)
    Definition Homo sapiens ARPIN-AP3S2 readthrough (ARPIN-AP3S2), mRNA.

    Target ORF information:

    Epitope DYKDDDDK
    Bacterial selection AMPR
    Mammalian selection NeoR
    Vector pcDNA3.1+/C-(K)DYK
    		 NM_001199058.1

    ORF Insert Sequence:

    1
    61
    121
    181
    241
    301
    361
    421
    481
    541
    601
    661
    721
    781
    841
    901
    961
    1021
    1081
    1141
    ATGAGCCGCA TCTACCACGA CGGCGCGCTC CGGAACAAGG CGGTGCAGAG CGTCCGGCTG 
    CCAGGGGCCT GGGACCCCGC CGCCCACCAG GGGGGAAATG GTGTCCTGCT GGAGGGAGAA 
    CTGATCGATG TATCTCGGCA CAGCATCTTG GACACTCATG GCAGGAAGGA GCGCTACTAC 
    GTGCTGTATA TCCGGCCCAG TCACATCCAT CGCCGTAAAT TCGACGCCAA GGGAAATGAA 
    ATCGAGCCCA ACTTCAGCGC CACCAGGAAG GTGAACACGG GCTTCCTCAT GTCGTCCTAC 
    AAGGTGGAAG CCAAGGGGGA CACTGACAGG CTCACGCCCG AGGCGCTGAA GGGGCTGGTC 
    AACAAGCCAG AGCTGCTCGC GCTGACAGAG AGCCTCACCC CCGACCACAC AGTGGCGTTC 
    TGGATGCCCG AGTCAGAGAT GGAGGTGATG GAACTCGAGC TGGGGGCCGG GGTACGGCTG 
    AAGACTCGGG GCGATGGTCC CTTCCTGGAT TCATTGGCCA AACTTGAGGC TGGAACAGTG 
    ACCAAGTGTA ATTTCACTGG TGATGGAAAG ACAGGGGCAT CCTGGACAGA CAACATCATG 
    GCCCAAAAGT GTTCGAAGGG GGCTGCAGCG GAGATCCGAG AGCAGGGGGA TGGGGCAGAG 
    GACGAGGAGT GGCCAGAAGA AATTCAACAG CAGATTGTTC GAGAGACTTT CCATCTAGTC 
    CTCAAGCGGG ATGACAACAT CTGTAACTTC TTGGAGGGTG GAAGTTTGAT TGGTGGCTCT 
    GACTACAAAC TGATCTACCG GCACTATGCT ACCCTCTACT TTGTATTTTG TGTGGATTCC 
    TCAGAGAGTG AACTTGGAAT CTTGGACCTC ATCCAGGTTT TTGTGGAAAC TCTGGATAAG 
    TGTTTCGAAA ATGTGTGTGA ATTGGATTTG ATCTTCCATA TGGATAAGGT GCACTACATC 
    CTCCAGGAGG TGGTGATGGG TGGGATGGTG TTGGAAACAA ACATGAATGA AATCGTGGCT 
    CAGATTGAGG CTCAAAACAG GCTGGAGAAA TCCGAGGGTG GCCTTTCAGC AGCCCCTGCG 
    CGGGCTGTGT CTGCTGTGAA AAACATCAAC CTGCCAGAGA TTCCTCGGAA CATCAACATT 
    GGCGATCTCA ACATCAAAGT TCCCAACCTG TCCCAGTTTG TCTGA

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

    ARPIN-AP3S2 ( NM_001199058.2 ) cDNA ORF clone, Homo sapiens(human) -> NP_001185987.1 Homo sapiens ARPIN-AP3S2 readthrough (ARPIN-AP3S2), mRNA.
    Price & Availability↑
    CloneID OHu12860
    Clone ID Related Accession (Same CDS sequence) NM_001199058.1 , NM_001199058.2
    Accession Version NM_001199058.2 Latest version! Documents for ORF clone product in default vector
    Sequence Information ORF Nucleotide Sequence (Length: 1185bp)
    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 2019-06-01
    Organism Homo sapiens(human)
    Product C15orf38-AP3S2 fusion protein
    Comment Comment: VALIDATED REFSEQ: This record has undergone validation or preliminary review. The reference sequence was derived from AC027176.23, AK000495.1 and AC018988.12. On Jun 2, 2019 this sequence version replaced NM_001199058.1. 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 :: SRR1803614.200208.1, SRR1803611.14599.1 [ECO:0000332] RNAseq introns :: mixed/partial sample support SAMEA1965299, SAMEA1966682 [ECO:0000350] ##Evidence-Data-END## ##RefSeq-Attributes-START## readthrough transcript :: includes exons from GeneID 10239, 348110 ##RefSeq-Attributes-END## COMPLETENESS: complete on the 3' end. 

    1
    61
    121
    181
    241
    301
    361
    421
    481
    541
    601
    661
    721
    781
    841
    901
    961
    1021
    1081
    1141
    ATGAGCCGCA TCTACCACGA CGGCGCGCTC CGGAACAAGG CGGTGCAGAG CGTCCGGCTG 
    CCAGGGGCCT GGGACCCCGC CGCCCACCAG GGGGGAAATG GTGTCCTGCT GGAGGGAGAA 
    CTGATCGATG TATCTCGGCA CAGCATCTTG GACACTCATG GCAGGAAGGA GCGCTACTAC 
    GTGCTGTATA TCCGGCCCAG TCACATCCAT CGCCGTAAAT TCGACGCCAA GGGAAATGAA 
    ATCGAGCCCA ACTTCAGCGC CACCAGGAAG GTGAACACGG GCTTCCTCAT GTCGTCCTAC 
    AAGGTGGAAG CCAAGGGGGA CACTGACAGG CTCACGCCCG AGGCGCTGAA GGGGCTGGTC 
    AACAAGCCAG AGCTGCTCGC GCTGACAGAG AGCCTCACCC CCGACCACAC AGTGGCGTTC 
    TGGATGCCCG AGTCAGAGAT GGAGGTGATG GAACTCGAGC TGGGGGCCGG GGTACGGCTG 
    AAGACTCGGG GCGATGGTCC CTTCCTGGAT TCATTGGCCA AACTTGAGGC TGGAACAGTG 
    ACCAAGTGTA ATTTCACTGG TGATGGAAAG ACAGGGGCAT CCTGGACAGA CAACATCATG 
    GCCCAAAAGT GTTCGAAGGG GGCTGCAGCG GAGATCCGAG AGCAGGGGGA TGGGGCAGAG 
    GACGAGGAGT GGCCAGAAGA AATTCAACAG CAGATTGTTC GAGAGACTTT CCATCTAGTC 
    CTCAAGCGGG ATGACAACAT CTGTAACTTC TTGGAGGGTG GAAGTTTGAT TGGTGGCTCT 
    GACTACAAAC TGATCTACCG GCACTATGCT ACCCTCTACT TTGTATTTTG TGTGGATTCC 
    TCAGAGAGTG AACTTGGAAT CTTGGACCTC ATCCAGGTTT TTGTGGAAAC TCTGGATAAG 
    TGTTTCGAAA ATGTGTGTGA ATTGGATTTG ATCTTCCATA TGGATAAGGT GCACTACATC 
    CTCCAGGAGG TGGTGATGGG TGGGATGGTG TTGGAAACAA ACATGAATGA AATCGTGGCT 
    CAGATTGAGG CTCAAAACAG GCTGGAGAAA TCCGAGGGTG GCCTTTCAGC AGCCCCTGCG 
    CGGGCTGTGT CTGCTGTGAA AAACATCAAC CTGCCAGAGA TTCCTCGGAA CATCAACATT 
    GGCGATCTCA ACATCAAAGT TCCCAACCTG TCCCAGTTTG TCTGA

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

    RefSeq NP_001185987.1
    CDS118..1302
    Translation

    Target ORF information:

    RefSeq Version NM_001199058.2
    Organism Homo sapiens(human)
    Definition Homo sapiens ARPIN-AP3S2 readthrough (ARPIN-AP3S2), mRNA.

    Target ORF information:

    Epitope DYKDDDDK
    Bacterial selection AMPR
    Mammalian selection NeoR
    Vector pcDNA3.1+/C-(K)DYK
    		 NM_001199058.2

    ORF Insert Sequence:

    1
    61
    121
    181
    241
    301
    361
    421
    481
    541
    601
    661
    721
    781
    841
    901
    961
    1021
    1081
    1141
    ATGAGCCGCA TCTACCACGA CGGCGCGCTC CGGAACAAGG CGGTGCAGAG CGTCCGGCTG 
    CCAGGGGCCT GGGACCCCGC CGCCCACCAG GGGGGAAATG GTGTCCTGCT GGAGGGAGAA 
    CTGATCGATG TATCTCGGCA CAGCATCTTG GACACTCATG GCAGGAAGGA GCGCTACTAC 
    GTGCTGTATA TCCGGCCCAG TCACATCCAT CGCCGTAAAT TCGACGCCAA GGGAAATGAA 
    ATCGAGCCCA ACTTCAGCGC CACCAGGAAG GTGAACACGG GCTTCCTCAT GTCGTCCTAC 
    AAGGTGGAAG CCAAGGGGGA CACTGACAGG CTCACGCCCG AGGCGCTGAA GGGGCTGGTC 
    AACAAGCCAG AGCTGCTCGC GCTGACAGAG AGCCTCACCC CCGACCACAC AGTGGCGTTC 
    TGGATGCCCG AGTCAGAGAT GGAGGTGATG GAACTCGAGC TGGGGGCCGG GGTACGGCTG 
    AAGACTCGGG GCGATGGTCC CTTCCTGGAT TCATTGGCCA AACTTGAGGC TGGAACAGTG 
    ACCAAGTGTA ATTTCACTGG TGATGGAAAG ACAGGGGCAT CCTGGACAGA CAACATCATG 
    GCCCAAAAGT GTTCGAAGGG GGCTGCAGCG GAGATCCGAG AGCAGGGGGA TGGGGCAGAG 
    GACGAGGAGT GGCCAGAAGA AATTCAACAG CAGATTGTTC GAGAGACTTT CCATCTAGTC 
    CTCAAGCGGG ATGACAACAT CTGTAACTTC TTGGAGGGTG GAAGTTTGAT TGGTGGCTCT 
    GACTACAAAC TGATCTACCG GCACTATGCT ACCCTCTACT TTGTATTTTG TGTGGATTCC 
    TCAGAGAGTG AACTTGGAAT CTTGGACCTC ATCCAGGTTT TTGTGGAAAC TCTGGATAAG 
    TGTTTCGAAA ATGTGTGTGA ATTGGATTTG ATCTTCCATA TGGATAAGGT GCACTACATC 
    CTCCAGGAGG TGGTGATGGG TGGGATGGTG TTGGAAACAA ACATGAATGA AATCGTGGCT 
    CAGATTGAGG CTCAAAACAG GCTGGAGAAA TCCGAGGGTG GCCTTTCAGC AGCCCCTGCG 
    CGGGCTGTGT CTGCTGTGAA AAACATCAAC CTGCCAGAGA TTCCTCGGAA CATCAACATT 
    GGCGATCTCA ACATCAAAGT TCCCAACCTG TCCCAGTTTG TCTGA

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

  • PubMed

    Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility.
    Nature genetics46(3)234-44(2014 Mar)
    ,,,,,Mahajan A,Go MJ,Zhang W,Below JE,Gaulton KJ,Ferreira T,Horikoshi M,Johnson AD,Ng MC,Prokopenko I,Saleheen D,Wang X,Zeggini E,Abecasis GR,Adair LS,Almgren P,Atalay M,Aung T,Baldassarre D,Balkau B,Bao Y,Barnett AH,Barroso I,Basit A,Been LF,Beilby J,Bell GI,Benediktsson R,Bergman RN,Boehm BO,Boerwinkle E,Bonnycastle LL,Burtt N,Cai Q,Campbell H,Carey J,Cauchi S,Caulfield M,Chan JC,Chang LC,Chang TJ,Chang YC,Charpentier G,Chen CH,Chen H,Chen YT,Chia KS,Chidambaram M,Chines PS,Cho NH,Cho YM,Chuang LM,Collins FS,Cornelis MC,Couper DJ,Crenshaw AT,van Dam RM,Danesh J,Das D,de Faire U,Dedoussis G,Deloukas P,Dimas AS,Dina C,Doney AS,Donnelly PJ,Dorkhan M,van Duijn C,Dupuis J,Edkins S,Elliott P,Emilsson V,Erbel R,Eriksson JG,Escobedo J,Esko T,Eury E,Florez JC,Fontanillas P,Forouhi NG,Forsen T,Fox C,Fraser RM,Frayling TM,Froguel P,Frossard P,Gao Y,Gertow K,Gieger C,Gigante B,Grallert H,Grant GB,Grrop LC,Groves CJ,Grundberg E,Guiducci C,Hamsten A,Han BG,Hara K,Hassanali N,Hattersley AT,Hayward C,Hedman AK,Herder C,Hofman A,Holmen OL,Hovingh K,Hreidarsson AB,Hu C,Hu FB,Hui J,Humphries SE,Hunt SE,Hunter DJ,Hveem K,Hydrie ZI,Ikegami H,Illig T,Ingelsson E,Islam M,Isomaa B,Jackson AU,Jafar T,James A,Jia W,J?ckel KH,Jonsson A,Jowett JB,Kadowaki T,Kang HM,Kanoni S,Kao WH,Kathiresan S,Kato N,Katulanda P,Keinanen-Kiukaanniemi KM,Kelly AM,Khan H,Khaw KT,Khor CC,Kim HL,Kim S,Kim YJ,Kinnunen L,Klopp N,Kong A,Korpi-Hy?v?lti E,Kowlessur S,Kraft P,Kravic J,Kristensen MM,Krithika S,Kumar A,Kumate J,Kuusisto J,Kwak SH,Laakso M,Lagou V,Lakka TA,Langenberg C,Langford C,Lawrence R,Leander K,Lee JM,Lee NR,Li M,Li X,Li Y,Liang J,Liju S,Lim WY,Lind L,Lindgren CM,Lindholm E,Liu CT,Liu JJ,Lobbens S,Long J,Loos RJ,Lu W,Luan J,Lyssenko V,Ma RC,Maeda S,M?gi R,M?nnisto S,Matthews DR,Meigs JB,Melander O,Metspalu A,Meyer J,Mirza G,Mihailov E,Moebus S,Mohan V,Mohlke KL,Morris AD,M?hleisen TW,M?ller-Nurasyid M,Musk B,Nakamura J,Nakashima E,Navarro P,Ng PK,Nica AC,Nilsson PM,Nj?lstad I,N?then MM,Ohnaka K,Ong TH,Owen KR,Palmer CN,Pankow JS,Park KS,Parkin M,Pechlivanis S,Pedersen NL,Peltonen L,Perry JR,Peters A,Pinidiyapathirage JM,Platou CG,Potter S,Price JF,Qi L,Radha V,Rallidis L,Rasheed A,Rathman W,Rauramaa R,Raychaudhuri S,Rayner NW,Rees SD,Rehnberg E,Ripatti S,Robertson N,Roden M,Rossin EJ,Rudan I,Rybin D,Saaristo TE,Salomaa V,Saltevo J,Samuel M,Sanghera DK,Saramies J,Scott J,Scott LJ,Scott RA,Segr? AV,Sehmi J,Sennblad B,Shah N,Shah S,Shera AS,Shu XO,Shuldiner AR,Sigur?sson G,Sijbrands E,Silveira A,Sim X,Sivapalaratnam S,Small KS,So WY,Stan??kov? A,Stefansson K,Steinbach G,Steinthorsdottir V,Stirrups K,Strawbridge RJ,Stringham HM,Sun Q,Suo C,Syv?nen AC,Takayanagi R,Takeuchi F,Tay WT,Teslovich TM,Thorand B,Thorleifsson G,Thorsteinsdottir U,Tikkanen E,Trakalo J,Tremoli E,Trip MD,Tsai FJ,Tuomi T,Tuomilehto J,Uitterlinden AG,Valladares-Salgado A,Vedantam S,Veglia F,Voight BF,Wang C,Wareham NJ,Wennauer R,Wickremasinghe AR,Wilsgaard T,Wilson JF,Wiltshire S,Winckler W,Wong TY,Wood AR,Wu JY,Wu Y,Yamamoto K,Yamauchi T,Yang M,Yengo L,Yokota M,Young R,Zabaneh D,Zhang F,Zhang R,Zheng W,Zimmet PZ,Altshuler D,Bowden DW,Cho YS,Cox NJ,Cruz M,Hanis CL,Kooner J,Lee JY,Seielstad M,Teo YY,Boehnke M,Parra EJ,Chambers JC,Tai ES,McCarthy MI,Morris AP


    Genome-wide association study identifies three novel loci for type 2 diabetes.
    Human molecular genetics23(1)239-46(2014 Jan)
    Hara K,Fujita H,Johnson TA,Yamauchi T,Yasuda K,Horikoshi M,Peng C,Hu C,Ma RC,Imamura M,Iwata M,Tsunoda T,Morizono T,Shojima N,So WY,Leung TF,Kwan P,Zhang R,Wang J,Yu W,Maegawa H,Hirose H,,Kaku K,Ito C,Watada H,Tanaka Y,Tobe K,Kashiwagi A,Kawamori R,Jia W,Chan JC,Teo YY,Shyong TE,Kamatani N,Kubo M,Maeda S,Kadowaki T


    Genome-wide association study in individuals of South Asian ancestry identifies six new type 2 diabetes susceptibility loci.
    Nature genetics43(10)984-9(2011 Aug)
    Kooner JS,Saleheen D,Sim X,Sehmi J,Zhang W,Frossard P,Been LF,Chia KS,Dimas AS,Hassanali N,Jafar T,Jowett JB,Li X,Radha V,Rees SD,Takeuchi F,Young R,Aung T,Basit A,Chidambaram M,Das D,Grundberg E,Hedman AK,Hydrie ZI,Islam M,Khor CC,Kowlessur S,Kristensen MM,Liju S,Lim WY,Matthews DR,Liu J,Morris AP,Nica AC,Pinidiyapathirage JM,Prokopenko I,Rasheed A,Samuel M,Shah N,Shera AS,Small KS,Suo C,Wickremasinghe AR,Wong TY,Yang M,Zhang F,,,Abecasis GR,Barnett AH,Caulfield M,Deloukas P,Frayling TM,Froguel P,Kato N,Katulanda P,Kelly MA,Liang J,Mohan V,Sanghera DK,Scott J,Seielstad M,Zimmet PZ,Elliott P,Teo YY,McCarthy MI,Danesh J,Tai ES,Chambers JC


    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


    Web-based, participant-driven studies yield novel genetic associations for common traits.
    PLoS genetics6(6)e1000993(2010 Jun)
    Eriksson N,Macpherson JM,Tung JY,Hon LS,Naughton B,Saxonov S,Avey L,Wojcicki A,Pe'er I,Mountain J


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