| 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.RY0402.237092_1 | Cre12.g521450 | CLPP2 | (1 of 1) PTHR10381//PTHR10381:SF11 - ATP-DEPENDENT CLP PROTEASE PROTEOLYTIC SUBUNIT // ATP-DEPENDENT CLP PROTEASE PROTEOLYTIC SUBUNIT, MITOCHONDRIAL-RELATED; peptidase subunit of mitochondrial ClpXP protease | intron | 73 |
| LMJ.RY0402.237092_2 | Cre13.g566400 | OPR55 | OctotricoPeptide Repeat protein 55; (1 of 19) PTHR21228//PTHR21228:SF20 - FAST LEU-RICH DOMAIN-CONTAINING // SUBFAMILY NOT NAMED | CDS | 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:
| Photosynthesis, screen 1 of 5 (No growth detected) |
| Photosynthesis, screen 3 of 5 (No growth detected) |
| Photosynthesis, screen 4 of 5 (No growth detected) |
| Photosynthesis, screen 5 of 5 (No growth detected) |
| Photosynthesis or light sensitivity, screen 1 of 12 (No growth detected) |
| Photosynthesis or light sensitivity, screen 5 of 12 (No growth detected) |
| Photosynthesis or light sensitivity, screen 6 of 12 (~30.0% growth defect) |
| Photosynthesis or light sensitivity, screen 7 of 12 (~70.0% growth defect) |
| Photosynthesis or light sensitivity, screen 8 of 12 (~90.0% growth defect) |
| Photosynthesis or light sensitivity, screen 9 of 12 (No growth detected) |
| Photosynthesis or light sensitivity, screen 10 of 12 (No growth detected) |
| Photosynthesis or light sensitivity, screen 11 of 12 (~80.0% growth defect) |
| Photosynthesis or light sensitivity, screen 12 of 12 (~60.0% 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.