Prp8 retinitis pigmentosa mutants cause defects in the transition between the catalytic steps of splicing.
Mayerle M, Guthrie C
RNA. 2016 May;22(5):793-809. doi: 10.1261/rna.055459.115. Epub 2016 Mar 11.
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Plasmids from Article
| ID | Plasmid | Purpose |
|---|---|---|
| 89966 | pRS313-PRP8 | complements prp8 genomic deletion |
| 89967 | pRS313-prp8-S2197F | S2197F point mutant |
| 89968 | pRS313-prp8-H2387P | H2387P point mutant |
| 89969 | pRS313-prp8-R2388G | R2388G point mutant |
| 89971 | pRS314-PRP16 | Prp16 in a trp backbone complements prp16 genomic deletion |
| 89972 | pRS314-prp16-1 | prp16-1 allele in TRP plasmid |
| 89973 | pRS314-prp16-101 | prp16-101 allele in TRP plasmid |
| 89974 | pRS314-prp16-302 | prp16-302 allele in TRP plasmid |