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.RY0402.224623_1 | Cre16.g676600 | (1 of 4) IPR029041 - FAD-linked oxidoreductase-like | intron | 73 |
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:
High temperature, screen 4 of 7 (~20.0% improved growth) |
LAT003D02, screen 1 of 1 (~50.0% growth defect) |
LAT007G11, screen 1 of 1 (~40.0% improved growth) |
LAT041A10, screen 1 of 1 (~70.0% improved growth) |
LAT041D08, screen 1 of 1 (~50.0% improved growth) |
Low pH, screen 3 of 3 (~50.0% growth defect) |
Photosynthesis, screen 1 of 5 (~20.0% growth defect) |
Photosynthesis or light sensitivity, screen 1 of 12 (~20.0% growth defect) |
Photosynthesis or light sensitivity, screen 2 of 12 (~40.0% growth defect) |
Photosynthesis or light sensitivity, screen 3 of 12 (~20.0% growth defect) |
Photosynthesis or light sensitivity, screen 4 of 12 (~50.0% growth defect) |
Photosynthesis or light sensitivity, screen 5 of 12 (~30.0% growth defect) |
Photosynthesis or light sensitivity, screen 6 of 12 (~20.0% growth defect) |
Photosynthesis or light sensitivity, screen 7 of 12 (~40.0% growth defect) |
Photosynthesis or light sensitivity, screen 8 of 12 (~50.0% growth defect) |
Photosynthesis or light sensitivity, screen 9 of 12 (~20.0% growth defect) |
Photosynthesis or light sensitivity, screen 10 of 12 (~30.0% growth defect) |
Photosynthesis or light sensitivity, screen 11 of 12 (~50.0% growth defect) |
Photosynthesis or light sensitivity, screen 12 of 12 (~40.0% growth defect) |
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.