| Arabidopsis thaliana |
AT4G32430 |
Mitochondrion |
nad1
|
265 |
CDS |
C-to-U |
CGG=>UGG |
R=>W |
Recoding |
|
Experiment Details
| Genotype (Ecotype) |
Allele |
Treatment |
Treatment Detail |
Mutant Type |
Phenotype |
Tissue |
Development Stage |
Detection Method |
Editing Frequency |
Editing Extent |
Mutant Effect |
PMID |
| NA | grs1-1 | T-DNA Insertion | T-DNA is located at 1325 bp downstream of the ATG start codon | Knockout | grs1-1 homozygotes are either lethal or exhibited growth retardation; cell division activity is reduced dramatically in the roots of grs1 plants | Seedling | 20 days | Direct Sequencing of PCR Products | 0.00% | Unedited | Absent | 27670716 | | NA | grs1-2 | T-DNA Insertion | T-DNA is inserted at 850 bp downstream of the ATG start codon | Knockout | Homozygous grs1-2 plants are found to phenocopy grs1-1 homozygous plants | Seedling | 20 days | Direct Sequencing of PCR Products | 0.00% | Unedited | None | 27670716 | | qrt 1 | WT | Control | Control | Control | Normal | Seedling | 20 days | Direct Sequencing of PCR Products | 100.00% | Complete | None | 27670716 | | NA | grs1-1 complemented lines | Complementation | Genomic complemented lines | Homozygous | No obvious differences compared to the wild-type | Seedling | 20 days | Direct Sequencing of PCR Products | 100.00% | Complete | Restored | 27670716 |
|
| Arabidopsis thaliana |
NA |
Mitochondrion |
nad1
|
265 |
CDS |
C-to-U |
NA=>NA |
NA=>NA |
NA |
|
Experiment Details
| Genotype (Ecotype) |
Allele |
Treatment |
Treatment Detail |
Mutant Type |
Phenotype |
Tissue |
Development Stage |
Detection Method |
Editing Frequency |
Editing Extent |
Mutant Effect |
PMID |
| Col-0 | WT | Control | Control | Control | NA | NA | NA | RNA-seq | 99.05% | High | None | 32098170 | | Col-0 | WT | Control | Control | Control | Normal | Leaf | NA | RT-PCR and calculated with the DNADynamo software (BlueTract | 100.00% | Complete | None | 28761003 | | Col-0 | DYW2-GFP-OE1 | Generating Arabidopsis plants overexpressing the GFP-tagged DYW2 gene | Col-0 A. thaliana plants were transformed with the 35S::DYW2-GFP plasmids (in pK7WGF2 backbone) by the floral-dip method. Transformed plants were selected based on Kanamycin resistance. Two independen | NA | Slow growth | Leaf | NA | RT-PCR and calculated with the DNADynamo software (BlueTract | 32.00% | Low | Decreased | 28761003 | | Col-0 | DYW2-GFP-OE2 | Generating Arabidopsis plants overexpressing the GFP-tagged DYW2 gene | Col-0 A. thaliana plants were transformed with the 35S::DYW2-GFP plasmids (in pK7WGF2 backbone) by the floral-dip method. Transformed plants were selected based on Kanamycin resistance. Two independen | NA | Slow growth | Leaf | NA | RT-PCR and calculated with the DNADynamo software (BlueTract | 11.00% | Poor | Decreased | 28761003 |
|
| Arabidopsis thaliana |
AT4G32430 |
Mitochondrion |
nad4L
|
55 |
CDS |
C-to-U |
CGG=>UGG |
R=>W |
Recoding |
|
Experiment Details
| Genotype (Ecotype) |
Allele |
Treatment |
Treatment Detail |
Mutant Type |
Phenotype |
Tissue |
Development Stage |
Detection Method |
Editing Frequency |
Editing Extent |
Mutant Effect |
PMID |
| NA | grs1-1 | T-DNA Insertion | T-DNA is located at 1325 bp downstream of the ATG start codon | Knockout | grs1-1 homozygotes are either lethal or exhibited growth retardation; cell division activity is reduced dramatically in the roots of grs1 plants | Seedling | 20 days | Direct Sequencing of PCR Products | 0.00% | Unedited | Absent | 27670716 | | NA | grs1-2 | T-DNA Insertion | T-DNA is inserted at 850 bp downstream of the ATG start codon | Knockout | Homozygous grs1-2 plants are found to phenocopy grs1-1 homozygous plants | Seedling | 20 days | Direct Sequencing of PCR Products | 0.00% | Unedited | None | 27670716 | | qrt 1 | WT | Control | Control | Control | Normal | Seedling | 20 days | Direct Sequencing of PCR Products | 100.00% | Complete | None | 27670716 | | NA | grs1-1 complemented lines | Complementation | Genomic complemented lines | Homozygous | No obvious differences compared to the wild-type | Seedling | 20 days | Direct Sequencing of PCR Products | 100.00% | Complete | Restored | 27670716 |
|
| Arabidopsis thaliana |
NA |
Mitochondrion |
nad4L
|
55 |
CDS |
C-to-U |
NA=>NA |
NA=>NA |
NA |
|
Experiment Details
| Genotype (Ecotype) |
Allele |
Treatment |
Treatment Detail |
Mutant Type |
Phenotype |
Tissue |
Development Stage |
Detection Method |
Editing Frequency |
Editing Extent |
Mutant Effect |
PMID |
| Col-0 | WT | Control | Control | Control | NA | NA | NA | RNA-seq | 94.28% | High | None | 32098170 | | Col-0 | WT | Control | Control | Control | Normal | Leaf | NA | RT-PCR and calculated with the DNADynamo software (BlueTract | 95.00% | High | None | 28761003 | | Col-0 | DYW2-GFP-OE1 | Generating Arabidopsis plants overexpressing the GFP-tagged DYW2 gene | Col-0 A. thaliana plants were transformed with the 35S::DYW2-GFP plasmids (in pK7WGF2 backbone) by the floral-dip method. Transformed plants were selected based on Kanamycin resistance. Two independen | NA | Slow growth | Leaf | NA | RT-PCR and calculated with the DNADynamo software (BlueTract | 32.00% | Low | Decreased | 28761003 | | Col-0 | DYW2-GFP-OE2 | Generating Arabidopsis plants overexpressing the GFP-tagged DYW2 gene | Col-0 A. thaliana plants were transformed with the 35S::DYW2-GFP plasmids (in pK7WGF2 backbone) by the floral-dip method. Transformed plants were selected based on Kanamycin resistance. Two independen | NA | Slow growth | Leaf | NA | RT-PCR and calculated with the DNADynamo software (BlueTract | 17.00% | Poor | Decreased | 28761003 |
|
| Arabidopsis thaliana |
AT4G32430 |
Mitochondrion |
nad6
|
103 |
CDS |
C-to-U |
CGC=>UGC |
R=>C |
Recoding |
|
Experiment Details
| Genotype (Ecotype) |
Allele |
Treatment |
Treatment Detail |
Mutant Type |
Phenotype |
Tissue |
Development Stage |
Detection Method |
Editing Frequency |
Editing Extent |
Mutant Effect |
PMID |
| NA | grs1-1 | T-DNA Insertion | T-DNA is located at 1325 bp downstream of the ATG start codon | Knockout | grs1-1 homozygotes are either lethal or exhibited growth retardation; cell division activity is reduced dramatically in the roots of grs1 plants | Seedling | 20 days | Direct Sequencing of PCR Products | 0.00% | Unedited | Absent | 27670716 | | NA | grs1-2 | T-DNA Insertion | T-DNA is inserted at 850 bp downstream of the ATG start codon | Knockout | Homozygous grs1-2 plants are found to phenocopy grs1-1 homozygous plants | Seedling | 20 days | Direct Sequencing of PCR Products | 0.00% | Unedited | None | 27670716 | | qrt 1 | WT | Control | Control | Control | Normal | Seedling | 20 days | Direct Sequencing of PCR Products | 100.00% | Complete | None | 27670716 | | NA | grs1-1 complemented lines | Complementation | Genomic complemented lines | Homozygous | No obvious differences compared to the wild-type | Seedling | 20 days | Direct Sequencing of PCR Products | 100.00% | Complete | Restored | 27670716 |
|
| Arabidopsis thaliana |
NA |
Mitochondrion |
nad6
|
103 |
CDS |
C-to-U |
NA=>NA |
NA=>NA |
NA |
|
Experiment Details
| Genotype (Ecotype) |
Allele |
Treatment |
Treatment Detail |
Mutant Type |
Phenotype |
Tissue |
Development Stage |
Detection Method |
Editing Frequency |
Editing Extent |
Mutant Effect |
PMID |
| Col-0 | WT | Control | Control | Control | NA | NA | NA | RNA-seq | 98.34% | High | None | 32098170 | | Col-0 | WT | Control | Control | Control | Normal | Leaf | NA | RT-PCR and calculated with the DNADynamo software (BlueTract | 98.00% | High | None | 28761003 | | Col-0 | DYW2-GFP-OE1 | Generating Arabidopsis plants overexpressing the GFP-tagged DYW2 gene | Col-0 A. thaliana plants were transformed with the 35S::DYW2-GFP plasmids (in pK7WGF2 backbone) by the floral-dip method. Transformed plants were selected based on Kanamycin resistance. Two independen | NA | Slow growth | Leaf | NA | RT-PCR and calculated with the DNADynamo software (BlueTract | 21.00% | Low | Decreased | 28761003 | | Col-0 | DYW2-GFP-OE2 | Generating Arabidopsis plants overexpressing the GFP-tagged DYW2 gene | Col-0 A. thaliana plants were transformed with the 35S::DYW2-GFP plasmids (in pK7WGF2 backbone) by the floral-dip method. Transformed plants were selected based on Kanamycin resistance. Two independen | NA | Slow growth | Leaf | NA | RT-PCR and calculated with the DNADynamo software (BlueTract | 1.00% | Poor | Decreased | 28761003 |
|
| Arabidopsis thaliana |
AT4G32430 |
Mitochondrion |
rps4
|
377 |
CDS |
C-to-U |
CCG=>CUG |
P=>L |
Recoding |
|
Experiment Details
| Genotype (Ecotype) |
Allele |
Treatment |
Treatment Detail |
Mutant Type |
Phenotype |
Tissue |
Development Stage |
Detection Method |
Editing Frequency |
Editing Extent |
Mutant Effect |
PMID |
| NA | grs1-1 | T-DNA Insertion | T-DNA is located at 1325 bp downstream of the ATG start codon | Knockout | grs1-1 homozygotes are either lethal or exhibited growth retardation; cell division activity is reduced dramatically in the roots of grs1 plants | Seedling | 20 days | Direct Sequencing of PCR Products | 0.00% | Unedited | Absent | 27670716 | | NA | grs1-2 | T-DNA Insertion | T-DNA is inserted at 850 bp downstream of the ATG start codon | Knockout | Homozygous grs1-2 plants are found to phenocopy grs1-1 homozygous plants | Seedling | 20 days | Direct Sequencing of PCR Products | 0.00% | Unedited | None | 27670716 | | qrt 1 | WT | Control | Control | Control | Normal | Seedling | 20 days | Direct Sequencing of PCR Products | 100.00% | Complete | None | 27670716 | | NA | grs1-1 complemented lines | Complementation | Genomic complemented lines | Homozygous | No obvious differences compared to the wild-type | Seedling | 20 days | Direct Sequencing of PCR Products | 100.00% | Complete | Restored | 27670716 |
|
| Arabidopsis thaliana |
NA |
Mitochondrion |
rps4
|
377 |
CDS |
C-to-U |
NA=>NA |
NA=>NA |
NA |
|
Experiment Details
| Genotype (Ecotype) |
Allele |
Treatment |
Treatment Detail |
Mutant Type |
Phenotype |
Tissue |
Development Stage |
Detection Method |
Editing Frequency |
Editing Extent |
Mutant Effect |
PMID |
| Col-0 | WT | Control | Control | Control | NA | NA | NA | RNA-seq | 87.31% | High | None | 32098170 | | Col-0 | WT | Control | Control | Control | Normal | Leaf | NA | RT-PCR and calculated with the DNADynamo software (BlueTract | 100.00% | Complete | None | 28761003 | | Col-0 | DYW2-GFP-OE1 | Generating Arabidopsis plants overexpressing the GFP-tagged DYW2 gene | Col-0 A. thaliana plants were transformed with the 35S::DYW2-GFP plasmids (in pK7WGF2 backbone) by the floral-dip method. Transformed plants were selected based on Kanamycin resistance. Two independen | NA | Slow growth | Leaf | NA | RT-PCR and calculated with the DNADynamo software (BlueTract | 2.00% | Poor | Decreased | 28761003 | | Col-0 | DYW2-GFP-OE2 | Generating Arabidopsis plants overexpressing the GFP-tagged DYW2 gene | Col-0 A. thaliana plants were transformed with the 35S::DYW2-GFP plasmids (in pK7WGF2 backbone) by the floral-dip method. Transformed plants were selected based on Kanamycin resistance. Two independen | NA | Slow growth | Leaf | NA | RT-PCR and calculated with the DNADynamo software (BlueTract | 0.00% | Unedited | Absent | 28761003 |
|