Skip to main content

Table 1 Primer sequences for PCR, fragment analysis and Sanger sequencing

From: Updated carrier rates for c.35delG (GJB2) associated with hearing loss in Russia and common c.35delG haplotypes in Siberia

c.35delG and studied markers (localization, GRCh38.p12)a

Primer sequences

Methods of detection

c.35delG

(GJB2)

(13:20189547)

F: 5′-GGTGAGGTTGTGTAAGAGTTGG-3′

R: 5’-CTGGTGGAGTGTTTGTTCC*CAC-3’

PCR-mediated site-directed mutagenesis (PSDM) with use of Bsc4 I

D13S141b

(13:20150320–20,150,445)

F: 5’-GTCCTCCCGGCCTAGTCTTA-3’ (6-FAM)

R: 5’-ACCACGGAGCAAAGAACAGA-3’

Fragment analysis (GeneScan 500 LIZ) on ABI 3130XL (Applied Biosystems)

D13S175b

(13:20274367–20,274,479)

F: 5’-TATTGGATACTTGAATCTGCTG-3’ (PET)

R: 5’-TGCATCACCTCACATAGGTTA-3’

D13S1853b

(13:20466607–20,466,800)

F: 5’- CAGACTGGCACAAACTTAACTG −3’ (6-FAM)

R: 5’- TGTACATCTCTTCTTACATTCATGT − 3’

rs3751385

(13:20188817)

F: 5’-GGCTGGTGAAGTGCAACG-3′

R: 5’-GTAAGCAAACAAACTTTTGAAGTAG-3’

PCR-RFLP analysis with use of Nhe I

  1. aLocalization was taken from the Ensembl Genome browser [53]; b - Specific primer sequences for PCR amplification of microsatellites D13S141, D13S175, and D13S1853 were obtained from the Ensembl genome browser and the NCBI Probe Database [53, 54], one from each primer pairs was labeled with the fluorescent dyes