From: Novel biallelic loss-of-function variants in CEP290 cause Joubert syndrome in two siblings
Primers | Forward | Reversed |
---|---|---|
CEP290 SNV | 5′ TAAATTCCACAGAGCCGATAAA 3′ | 5′ ACAGCCCAAGAAATGAGGTT 3′ |
CEP290 exon 1 | 5′ GTTCCACGCCTTCTCATCAT 3′ | 5′ TGCCAGGAGAGCCTACAGTT 3′ |
CEP290 exon 2 | 5′ AGGTGGAGCACAGTGAAAGAA 3′ | 5′ TCTGCCAGTTCTTCTTGACG 3′ |
CEP290 exon 6 | 5′ AGTCTGCAGGTGGACGAGAT 3′ | 5′ CCAACTCCTTTTCCATGTCC 3′ |
CEP290 exon 7 | 5′ CAGCCTAGGCGACAAAGACT 3′ | 5′ CCTTTGTTGAACCACCACAA 3′ |
CEP290 exon 10 | 5′ GGACACTTATGGCTGCGTTT 3′ | 5′ CATCAGTCATCTTCTCCATTTCC 3′ |
CEP290 exon 11 | 5′ CATCAGTTTGCAACAACTCTTGA 3′ | 5′ TTTTGCATTGACAGCTACCAT 3′ |
CEP290 mRNA | 5′ AAAGTTGACCCAGATGACCT 3′ | 5′ AAACCGAGTATCTCGTCCAC 3′ |
Human GAPDH | 5′ ATGTTCGTCATGGGTGTGAA 3′ | 5′ GTCTTCTGGGTGGCAGTGAT 3′ |