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. Author manuscript; available in PMC: 2014 Jun 1.
Published in final edited form as: Eur J Med Genet. 2013 Mar 19;56(6):292–296. doi: 10.1016/j.ejmg.2013.03.002

Table 1. Primers used for PCR amplification and sequencing.

Primers for PCR amplification of MYOC gene and Sanger sequencing. One pair of primers was used for promoter region and Exon 1 including exon-intron junction, two pairs of primers were used for Exon 3 including exon-intron junctions. Four sets of primers used for haplotype analysis by genotyping SNPs are shown with respective SNP rs numbers. The Amplicon sizes of amplicons were are shown in base pairs (bp).

Name Sequence (5′ – 3′) Target Amplicon Size (bp)
M1.1F GGTGCATAAATTGGGATGTTC Promoter & Exon 1 999
M1.1R TTGTGCTAGCTGTGCAGTCTC
M3-3F TGCGATAACTGAGGCGTAGAG Exon 3 (Part 1) 997
M3-3R GGAGGCTTTTCACATCTTGG
M3-2F CATTGACTTGGCTGTGGATG Exon 3 (Part 2) 992
M3.1R CATCCTGCAATCACATCTCC
MS5F CTCAATGAGTTTGCAGAGTG rs235920 399
MS5R TCTGCTGTGCTGAGAGGTG
MS89F TGAACCTTTGCTCAGATTG rs235918 399
MS89R CCACTTTCACAAAAAGTGAC
MS4F GTCCTGAACACCTGAGAATC rs235868 396
MS4R GTAAGCAGGTTTAGGATTGG
MS2F CTCAGGCCCAACTGTTATC rs603930 295
MS2R AGAATTAGCTGGATGTGGTG