| 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.RY0402.173761_1 | Cre05.g248650 | (1 of 587) 2.7.11.1 - Non-specific serine/threonine protein kinase / Threonine-specific protein kinase | intron | 73 | |
| LMJ.RY0402.173761_2 | Cre10.g430900 | (1 of 1) IPR000104//IPR007259 - Antifreeze protein, type I // Gamma-tubulin complex component protein | CDS | 58 | |
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:
| Hydroxyurea, screen 1 of 2 (~30.0% growth defect) |
| LAT003D02, screen 1 of 1 (~50.0% growth defect) |
| LAT003D07, screen 1 of 1 (~20.0% improved growth) |
| LAT030B09, screen 1 of 1 (~20.0% growth defect) |
| LAT030E11, screen 1 of 1 (~30.0% growth defect) |
| LAT032D03, screen 1 of 1 (No phenotype detected) |
| LAT032H10, screen 1 of 1 (~30.0% growth defect) |
| LAT034B04, screen 1 of 1 (~20.0% growth defect) |
| LAT034H07, screen 1 of 1 (~40.0% growth defect) |
| LAT035F03, screen 1 of 1 (~30.0% growth defect) |
| LAT035G03, screen 1 of 1 (~10.0% improved growth) |
| LAT035H07, screen 1 of 1 (~40.0% growth defect) |
| LAT041D10, screen 1 of 1 (~30.0% growth defect) |
| LAT042C03, screen 1 of 1 (~50.0% growth defect) |
| Limited growth in liquid media, screen 3 of 4 (~20.0% growth defect) |
| Limited growth in liquid media, screen 4 of 4 (No phenotype detected) |
| Low Termperature, screen 1 of 1 (~40.0% growth defect) |
| Photosynthesis or light sensitivity, screen 2 of 12 (~20.0% growth defect) |
| Photosynthesis or light sensitivity, screen 4 of 12 (~10.0% improved growth) |
| Zeocin, screen 5 of 5 (No phenotype detected) |
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.