Mutation DE(ruvB-ruvA)799::(apra)
- Name: DE(ruvB-ruvA)799::(apra)
- Type: Deletion
- Approx. Map Location: 41.86
- Properties
Property Symbol Apramycin resistant apra - Comments
- The deletion starts 39bp into ruvA and extends to 39bp from the end of ruvB. The deletion/insertion joints are as follows with chromosomal sequence in uppercase and apramycin cassette in lowercase: ATTGAAAAA/tcatgtgca..........tctgggcgg/TGGAATCAC.
- References
- 1 Strains Carrying This Mutation
Name Mutations Genotype N6029 3 F-, λ-, Δ(ruvB-ruvA)799(::apra), rph-1