Primers and allele-specific oligonucleotides
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Primers
VNTR amplification primers
Name Sequence
INS-1296 CTGCTGAGGACTTGCTGCTTG
INS-23+ CAGAAGGACAGTGATCTGGGT
INS-23- CAGAAGGACAGTGATCTGGGA
MVR-PCR primers
Name Sequence
TAG TCATGCGTCCATGGTCCGGA
INS-MA TCATGCGTCCATGGTCCGGAACCCCTGTCCCCAC
INS-MB TCATGCGTCCATGGTCCGGAACCCCTGTCCCCAGG
INS-MC TCATGCGTCCATGGTCCGGAACCCCTGTCCCCAG
INS-ME TCATGCGTCCATGGTCCGGAACCCCTATCCCCAC
INS-MF TCATGCGTCCATGGTCCGGAACCCCTGTCCCCGGG
INS-MH TCATGCGTCCATGGTCCGGAACCCCTGTGCCCAC
Primers for fragmenting large alleles
Name Sequence
INS-MBR CTGCTGAGGACTTGCTGCTTGGGGGACAGGGGTCCT
INS-MEF CAGAAGGACAGTGATCTGGGATCCCCACACCCCTA
INS-MER CTGCTGAGGACTTGCTGCTTGCAGGGGTGTGGGGAT
INS-MFF CAGAAGGACAGTGATCTGGGAACCCCTGTCCCCGGG
INS-MFR CTGCTGAGGACTTGCTGCTTGGGGGACAGGGGTCCC
INS-MHF CAGAAGGACAGTGATCTGGGACCCACACCCCTGTG
INS-MHR CTGCTGAGGACTTGCTGCTTGACAGGGGTGTGGGC
Sequencing primers
Name Sequence
5F1 GAGCAGGGCTGGACCTGTGA
5F2 CCCGGCAGTCTCTAGTGGAA
5F3 GCACCTGCTTCTCAGCGCAA
5F4 TCCCAGCCCTTGAGAGAAACA
5F5 GGGTGTCTCTGAAGGGCTGT
5F6 CTGGTGCTAAGAGGCAGGTA
5R1 GCCGCCATGGATGGGCCAA
3F1 CCTCCAGCTCTCCTGGTCTA
3F2 GACGTGGCTGGGCTCGTGAA
3R4 GCACACTAGGTAGAGAGCTTC
3F8 GAGGCTTCTTCTACACACCCAA
3F3 TCCCTGTGGCCCAGTCAGAA
3F4 GTGGGTGACCCTCCCTCTAA
3F5 GGGTGCCCACAGGTGCCAA
3F6 GCCCAGGTCCAGCCAGACA
3F6-NEST CCACTGGTGCCTTGGAGGAA
3R5 TGCAATCCTCAGGGCCTCAT
3R3 TGCTTCTCCTGGGCTGCAATC
3F7 TGCTGGAGCTGAGGTATGTGA
3R2 ACAGCTTGGCCGATGGCTGA
3R1-NEST GGAGCAGTTAGATGGACCCAA
3R1 CTTGTGACTGGGGAGCAGTTA
Allele-specific oligonucleotides
SNP Allele Sequence
INS-1 C 5´-CCCCTGGCTGCAGCAGCC-3´
T 5´-CCCCTGGTTGCAGCAGCC-3´
INS-2 A 5´-TGAGGACATCCTGTGGAA-3´
G 5´-TGAGGACGTCCTGTGGAA-3´
INS-3 C 5´-CCCCCTGCCCTGGGATGG-3´
T 5´-CCCCCTGTCCTGGGATGG-3´
INS-4 C 5´-GAGCCACCGTGAAGGTGG-3´
T 5´-GAGCCACTGTGAAGGTGG-3´
INS-5 C 5´-CCATCGACGTGCTGGACA-3´
T 5´-CCATCGATGTGCTGGACA-3´
INS-6 A 5´-AATCACCATCACAATAAA-3´
G 5´-AATCACCGTCACAATAAA-3´
INS-7 C 5´-CCACAGACACAGACCCTG-3´
G 5´-CCACAGAGACAGACCCTG-3´
INS-9 A 5´-GGCCTGGAAGGGAGCAGG-3´
C 5´-GGCCTGGCAGGGAGCAGG-3´
INS-10 C 5´-CACTACACGCTGCTGGGA-3´
T 5´-CACTACATGCTGCTGGGA-3´
INS-11 C 5´-AGCTCCCCGGCCGACAAC-3´
T 5´-AGCTCCCTGGCCGACAAC-3´
INS-12 C 5´-CTCCCCCCATCCAGCCTC-3´
T 5´-CTCCCCCTATCCAGCCTC-3´
INS-14 C 5´-GAAAGGGCGGAAGGGAGG-3´
T 5´-GAAAGGGTGGAAGGGAGG-3´
INS-16 A 5´-AGGCTAAGGCCAGGGTGG-3´
G 5´-AGGCTGAGGCCAGGGTGG-3´
INS-17 A 5´-GGTGTCAAGGGACCTGGC-3´
T 5´-GGTGTCATGGGACCTGGC-3´
INS-18 A 5´-TGCCGCCACCCCCAGATC-3´
G 5´-TGCCGCCGCCCCCAGATC-3´
INS-19 C 5´-GATCACACGGAAGATGAG-3´
T 5´-GATCACATGGAAGATGAG-3´
INS-20 C 5´-CAGGTCCCCAGGTCATGC-3´
T 5´-CAGGTCCTCAGGTCATGC-3´
INS-21 A 5´-CACTYCCACTCTCCCACC-3´
C 5´-CACTYCCCCTCTCCCACC-3´
INS-24 C 5´-GGGTTGACAGGTAGRGGA-3´
G 5´-GGGTTGAGAGGTAGRGGA-3´
INS-25 A 5´-AGGTAGAGGAGATGGGCT-3´
G 5´-AGGTAGGGGAGATGGGCT-3´
INS-69 + 5´-AGGTCTTTGCGTTCCAAG-3´
- 5´-GCAGGTCTGTTCCAAGGG-3´
INS-26 A 5´-GCTCARGATTCCAGGGTG-3´
G 5´-GCTCARGGTTCCAGGGTG-3´
INS-27 A 5´-GCCTGTCACCCAGATCAC-3´
T 5´-GCCTGTCTCCCAGATCAC-3´
INS-72 C 5´-TCACTGTCCTTCTGCCAT-3´
T 5´-TCACTGTTCTTCTGCCAT-3´
INS-70 A 5´-TGCTGGCACTGCTGGCCC-3´
G 5´-TGCTGGCGCTGCTGGCCC-3´
INS-28 C 5´-AGCCAACCGCCCATTGCT-3´
T 5´-AGCCAACTGCCCATTGCT-3´
INS-31 C 5´-GTGGGCACGCTCCTYCCT-3´
T 5´-GTGGGCATGCTCCTYCCT-3´
INS-32 C 5´-CTGCCTCCGGGCGAACAC-3´
T 5´-CTGCCTCTGGGCGAACAC-3´
INS-34 C 5´-ACACCCACTGTGGGTGAC-3´
G 5´-ACACCCAGTGTGGGTGAC-3´
INS-35 C 5´-GGGAGTGCGACCTAGGGC-3´
T 5´-GGGAGTGTGACCTAGGGC-3´
INS-36 A 5´-CCTCGCCACTGTTCCGGA-3´
G 5´-CCTCGCCGCTGTTCCGGA-3´
INS-37 C 5´-CTCTGCGCGGCACGTYCT-3´
T 5´-CTCTGCGTGGCACGTYCT-3´
INS-38 C 5´-CGCAGCCCGCAGGCAGCC-3´
T 5´-CGCAGCCTGCAGGCAGCC-3´
INS-39 A 5´-CAGCCCCACACCCGCCGC-3´
C 5´-CAGCCCCCCACCCGCCGC-3´
INS-40 C 5´-TGCCTGTCGGCTGCCTGC-3´
T 5´-TGCCTGTTGGCTGCCTGC-3´
INS-41 G 5´-GGGAGCTGCGGGGGTCTC-3´
T 5´-GGGAGCTTCGGGGGTCTC-3´
INS-42 A 5´-GCCAGGGATGGTGGGGCC-3´
G 5´-GCCAGGGGTGGTGGGGCC-3´
INS-43 C 5´-AGAGACCACGGCCAGGGT-3´
G 5´-AGAGACCAGGGCCAGGGT-3´
INS-45 C 5´-CTTAGCCCACCCCCTCCC-3´
T 5´-CTTAGCCTACCCCCTCCC-3´
INS-49 A 5´-GCTCCACCCAGGGCTGGG-3´
T 5´-GCTCCACCCTGGGCTGGG-3´
INS-71 + 5´-GCTGGGCTGGGGATGGCT-3´
- 5´-ACCCWGGGCTGGGGATGG-3´
INS-51 C 5´-GAGGCCCCTTCTGGGAGG-3´
G 5´-GAGGCCCGTTCTGGGAGG-3´
INS-52 A 5´-GGACCGTATGTTGGAGTG-3´
G 5´-GGACCGTGTGTTGGAGTG-3´
INS-53 A 5´-CTGGGGGATGAGGAGTGT-3´
C 5´-CTGGGGGCTGAGGAGTGT-3´
INS-54 C 5´-GTGTCTTCYGAGGGGCCA-3´
T 5´-GTGTCTTTYGAGGGGCCA-3´
INS-73 C 5´-GCAAGGCCGCCCACCCAA-3´
T 5´-GCAAGGCTGCCCACCCAA-3´
INS-56 A 5´-GCCCTGGACCAGAGCTGG-3´
G 5´-GCCCTGGGCCAGAGCTGG-3´
INS-74 A 5´-CCAGCACCTTGACCCCAC-3´
G 5´-CCAGCGCCTTGACCCCAC-3´
INS-57 A 5´-GGAGACCACAGCCAGGGC-3´
G 5´-GGAGACCGCAGCCAGGGC-3´
INS-60 A 5´-ATRAGAAACAGTTGGCCA-3´
G 5´-ATRAGAAGCAGTTGGCCA-3´
INS-63 C 5´-GRCAGCCCTTCAGTGTCC-3´
T 5´-GRCAGCCTTTCAGTGTCC-3´
INS-64 C 5´-GGAGCCTCGGYTTCACAT-3´
G 5´-GGAGCCTGGGYTTCACAT-3´
INS-65 C 5´-GCCTSGGCTTCACATGCC-3´
T 5´-GCCTSGGTTTCACATGCC-3´
INS-66 C 5´-TGCCCACCRGGCTGGCAG-3´
T 5´-TGCCCACTRGGCTGGCAG-3´
INS-67 A 5´-GCCCACYAGGCTGGCAGG-3´
G 5´-GCCCACYGGGCTGGCAGG-3´
INS-68 A 5´-CAGCCCCAGCGGTCACCC-3´
G 5´-CAGCCCCGGCGGTCACCC-3´
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These pages provide supplementary information for the following publications:
Global haplotype diversity in the human insulin gene region. Stead, J.D.H., Hurles, M.E. and Jeffreys, A.J. Genome Res. 13, 2101-11 (2003)
Structural analysis of insulin minisatellite alleles reveals unusually large differences in diversity between Africans and non-Africans. Stead, J.D.H. and Jeffreys, A.J. Am. J. Hum. Genet. 71, 1273-84 (2002)
Influence of allele lineage on the role of the insulin minisatellite in susceptibility to type 1 diabetes. Stead, J.D.H., Buard, J., Todd, J.A. and Jeffreys, A.J. Hum. Mol. Genet., 9, 2929-2935 (2000).
Allele diversity and germline mutation at the insulin minisatellite. Stead, J.D.H. and Jeffreys, A.J. Hum. Mol. Genet., 9, 713-723 (2000).
If you refer to these data, please cite the relevant publication.
Last updated: 8 September, 2005
Celia A. May
The views expressed in this document are those of the document owner, John D.H. Stead.