Mutation DE(ppc-argH)486
- Name: DE(ppc-argH)486
- Type: Deletion
- Approx. Map Location: 89.40
- Comments
- References
- 1 Strains Carrying This Mutation
Name Mutations Genotype MN42LAM- 7 Hfr(PO3), λ-, relA1, spoT1, metB1, Δ(ppc-argH)486, rrnB-2?, creC510
| Name | Mutations | Genotype |
|---|---|---|
| MN42LAM- | 7 | Hfr(PO3), λ-, relA1, spoT1, metB1, Δ(ppc-argH)486, rrnB-2?, creC510 |