| Arabidopsis thaliana |
AT4G21190 |
Chloroplast |
accD
|
1568 |
CDS |
TAIR |
NA |
NA |
NA |
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 |
| Columbia (Col-0) | WT | Wild type | No treatment | No mutant | Normal | Leaf | NA | The RT-PCR products were sequenced directly | 70.00% | High | None | 42480504 | | NA | EMB1417-RNAi-1 | Generation of inducible silencing lines | To obtain the Arabidopsis EMB1417 silencing constructs, two 300-bp regions from the coding sequence of EMB1417 gene were amplified by PCR; PCR products were cloned into the pBWA(V)HVE (Kanamycin, Kan) | Homozygous | A yellow-leaf phenotype with markedly reduced chlorophyll content | Leaf | NA | The RT-PCR products were sequenced directly | 22.00% | Low | Decreased | 42480504 |
|
| Arabidopsis thaliana |
AT4G21190 |
Chloroplast |
clpP
|
559 |
CDS |
TAIR |
NA |
NA |
NA |
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 |
| Columbia (Col-0) | WT | Wild type | No treatment | No mutant | Normal | Leaf | NA | The RT-PCR products were sequenced directly | 100.00% | Complete | None | 42480504 | | NA | EMB1417-RNAi-1 | Generation of inducible silencing lines | To obtain the Arabidopsis EMB1417 silencing constructs, two 300-bp regions from the coding sequence of EMB1417 gene were amplified by PCR; PCR products were cloned into the pBWA(V)HVE (Kanamycin, Kan) | Homozygous | A yellow-leaf phenotype with markedly reduced chlorophyll content | Leaf | NA | The RT-PCR products were sequenced directly | 55.00% | Medium | Decreased | 42480504 |
|
| Arabidopsis thaliana |
AT4G21190 |
Chloroplast |
ndhD
|
2 |
CDS |
TAIR |
NA |
NA |
NA |
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 |
| Columbia (Col-0) | WT | Wild type | No treatment | No mutant | Normal | Leaf | NA | The RT-PCR products were sequenced directly | 79.00% | High | None | 42480504 | | NA | EMB1417-RNAi-1 | Generation of inducible silencing lines | To obtain the Arabidopsis EMB1417 silencing constructs, two 300-bp regions from the coding sequence of EMB1417 gene were amplified by PCR; PCR products were cloned into the pBWA(V)HVE (Kanamycin, Kan) | Homozygous | A yellow-leaf phenotype with markedly reduced chlorophyll content | Leaf | NA | The RT-PCR products were sequenced directly | 6.00% | Poor | Decreased | 42480504 |
|
| Arabidopsis thaliana |
AT4G21190 |
Chloroplast |
petL
|
5 |
CDS |
TAIR |
NA |
NA |
NA |
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 |
| Columbia (Col-0) | WT | Wild type | No treatment | No mutant | Normal | Leaf | NA | The RT-PCR products were sequenced directly | 59.00% | Medium | None | 42480504 | | NA | EMB1417-RNAi-1 | Generation of inducible silencing lines | To obtain the Arabidopsis EMB1417 silencing constructs, two 300-bp regions from the coding sequence of EMB1417 gene were amplified by PCR; PCR products were cloned into the pBWA(V)HVE (Kanamycin, Kan) | Homozygous | A yellow-leaf phenotype with markedly reduced chlorophyll content | Leaf | NA | The RT-PCR products were sequenced directly | 4.00% | Poor | Decreased | 42480504 |
|
| Arabidopsis thaliana |
AT4G21190 |
Chloroplast |
psbZ
|
50 |
CDS |
TAIR |
NA |
NA |
NA |
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 |
| Columbia (Col-0) | WT | Wild type | No treatment | No mutant | Normal | Leaf | NA | The RT-PCR products were sequenced directly | 100.00% | Complete | None | 42480504 | | NA | EMB1417-RNAi-1 | Generation of inducible silencing lines | To obtain the Arabidopsis EMB1417 silencing constructs, two 300-bp regions from the coding sequence of EMB1417 gene were amplified by PCR; PCR products were cloned into the pBWA(V)HVE (Kanamycin, Kan) | Homozygous | A yellow-leaf phenotype with markedly reduced chlorophyll content | Leaf | NA | The RT-PCR products were sequenced directly | 22.00% | Low | Decreased | 42480504 |
|
| Arabidopsis thaliana |
AT4G21190 |
Chloroplast |
rpoA
|
200 |
CDS |
TAIR |
NA |
NA |
NA |
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 |
| Columbia (Col-0) | WT | Wild type | No treatment | No mutant | Normal | Leaf | NA | The RT-PCR products were sequenced directly | 100.00% | Complete | None | 42480504 | | NA | EMB1417-RNAi-1 | Generation of inducible silencing lines | To obtain the Arabidopsis EMB1417 silencing constructs, two 300-bp regions from the coding sequence of EMB1417 gene were amplified by PCR; PCR products were cloned into the pBWA(V)HVE (Kanamycin, Kan) | Homozygous | A yellow-leaf phenotype with markedly reduced chlorophyll content | Leaf | NA | The RT-PCR products were sequenced directly | 27.00% | Low | Decreased | 42480504 |
|