Mutant strain: LMJ.RY0402.237082

Overview

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.RY0402.237082_1 Cre12.g524500 RMT2 Putative protein N-methyltransferase; (1 of 2) PTHR13271//PTHR13271:SF30 - UNCHARACTERIZED PUTATIVE METHYLTRANSFERASE // SUBFAMILY NOT NAMED intron 58
LMJ.RY0402.237082_2 Cre12.g553800 (1 of 1) IPR002110//IPR020683//IPR029071 - Ankyrin repeat // Ankyrin repeat-containing domain // Ubiquitin-related domain 3'UTR 73

If you use this mutant for your work, please cite: Li et al. 2019 Nature Genetics.

Phenotypes

This mutant exhibited a phenotype under the following conditions:

Photosynthesis, screen 1 of 5 (No growth detected)
Photosynthesis, screen 3 of 5 (~90.0% growth defect)
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 2 of 12 (No growth detected)
Photosynthesis or light sensitivity, screen 3 of 12 (No growth detected)
Photosynthesis or light sensitivity, screen 4 of 12 (No growth detected)
Photosynthesis or light sensitivity, screen 5 of 12 (No growth detected)
Photosynthesis or light sensitivity, screen 6 of 12 (~50.0% growth defect)
Photosynthesis or light sensitivity, screen 7 of 12 (~60.0% growth defect)
Photosynthesis or light sensitivity, screen 8 of 12 (~60.0% growth defect)
Photosynthesis or light sensitivity, screen 9 of 12 (~50.0% growth defect)
Photosynthesis or light sensitivity, screen 10 of 12 (~50.0% growth defect)
Photosynthesis or light sensitivity, screen 11 of 12 (~50.0% growth defect)
Photosynthesis or light sensitivity, screen 12 of 12 (~50.0% 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.