| Background strain: | cMJ030 | Click here to order this strain from the Chlamydomonas Resource Center. The background strain comes free with every order. |
| Transformation condition: | RY0402 | |
| Antibiotic resistance: | resistant to paromomycin |
Insertion junctions | |||||
| Insertion junction | Locus systematic id | Locus common name | Defline | Feature | Confidence (%) |
|---|---|---|---|---|---|
| LMJ.RY0402.119590_1 | Cre09.g396950 | MFT25,CGL15,PHT4I,PHT4-9 | Na+-dependent inorganic phosphate cotransporter; (1 of 4) K08193 - MFS transporter, ACS family, solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), other (SLC17A) | intron | 95 |
| LMJ.RY0402.119590_2 | Cre09.g396950 | MFT25,CGL15,PHT4I,PHT4-9 | Na+-dependent inorganic phosphate cotransporter; (1 of 4) K08193 - MFS transporter, ACS family, solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), other (SLC17A) | intron | 95 |
If you use this mutant for your work, please cite: Li et al. 2019 Nature Genetics.
This mutant exhibited a phenotype under the following conditions:
| Carbon concentrating mechanism, screen 1 of 11 (~20.0% improved growth) |
| Carbon concentrating mechanism, screen 2 of 11 (~10.0% improved growth) |
| Carbon concentrating mechanism, screen 3 of 11 (No phenotype detected) |
| Carbon concentrating mechanism, screen 4 of 11 (~30.0% growth defect) |
| Carbon concentrating mechanism, screen 5 of 11 (~10.0% growth defect) |
| Carbon concentrating mechanism, screen 6 of 11 (No phenotype detected) |
| Carbon concentrating mechanism, screen 7 of 11 (No phenotype detected) |
| Carbon concentrating mechanism, screen 10 of 11 (~10.0% growth defect) |
| Carbon concentrating mechanism, screen 11 of 11 (~20.0% improved growth) |
| High temperature, screen 1 of 7 (~30.0% growth defect) |
| Hypoxic, screen 1 of 1 (~20.0% improved growth) |
| Photosynthesis, screen 4 of 5 (~20.0% growth defect) |
| Photosynthesis, screen 5 of 5 (~10.0% improved growth) |
Note: Not all phenotypes can be confidently associated with a specific gene or insertion; phenotypes can be caused by unmapped second-site mutations. Please see the gene pages for statistically significant gene-phenotype links. These data are from a pooled phenotyping experiment.
If you reference the phenotypic data above in a manuscript, please cite: Fauser et al. 2022 Nature Genetics.