Table 1 of Chen, Mol Vis 2009; 15:1359-1365.


Table 1. Primers used for mutation screening.

Gene symbol
and amplified
fragments


Primer sequences
PCR
product size
(bp)
Annealing
temperature
(°C)
CRYAA


Exon 1 F:5′-CTCCAGGTCCCCGTGGTA-3′ 251 65
  R:5′-AGGAGAGGCCAGCACCAC-3′

Exon 2 F:5′-CTGTCTCTGCCAACCCCAG-3′ 220 65
  R:5′-CTGTCCCACCTCTCAGTGCC-3′

Exon 3 F:5′-GGCAGCTTCTCTGGCATG-3′ 309 65
  R:5′-GAGCCAGCCGAGGCAATG-3′

CRYAB


Exon 1 F:5′-TGCATATATAAGGGGCTGGCTGTA-3′ 363 65
  R:3′-CAGGGTAGGAAAGGAAAATGGATG-3′

Exon 2 F:5′-AGGATGAATTACCCGGACAGAAAG-3′ 220 60
  R:5′-ACCCCTGATCCCGACTGTTAT-3′

Exon 3 F:5′-TGAGTTCTGGGCAGGTGATAATAGTT-3′ 273 60
  R:5′-AGCTTGATAATTTGGGCCTGCC-3′

CRYBA1/A3 F:5′-CAATCCTCCCTCCACCTC-3′ 520 57
  R:3′-TCCTTCCTTCTAGCTTTGG-3′

CRYBB2


Exon 6 F:5′-CCCCTCGTTCACCCTCCCATCA-3′ 506 69
  R:5′-CACTGTGTCCAAGGTCACACAGCTAAGC-3′

CRYGC


Exons 1,2 F:5′-TCAATCATATAGACAGAGCCA-3′ 784 55
  R:5′-ATCTCCATCTAACCTTAGGT-3′

Exon 3 F:5′-AATGACAATTCCATGCCACA-3′ 534 55
  R:5′-CCCACCCCATTCACTTCTTA-3′

CRYGD


Exons 1,2 F:5′-TGATAGCAATCCGAATACTCCA-3′ 776 55
  R:5′-GGGTAATACTTTGCTTATGTGGGGAG-3′

Exon 3 F:5′-GTCCTCACCAAGCTGGACTG-3′ 496 55
  R:5′-CCATTTGCCTCGTGTGTGTA-3′

GJA8 F:5′-AGGAGGTGAATGAGCACTCCA-3′ 251 57
  R:5′-GTGCCCCACGTACATCAGG-3′

MIP F:5′-GAGGAGGTAACACTGTGGCAGC-3′ 198 60
  R:3′-AGAAGCCAACGGCCAGG-3′

BFSP2 F:5′-GCTGCTGCACAAACAGTTGG-3′ 286 62
  R:5′-TTCTGTTTCTAATGAGGTTGAACTTGTTA-3′

GJA3 F:5′-TGCAACACCCAGCAGCC-3′ 474 60
  R:5′-GGCCACCGCCAGCAT-3′