Common name: | SUB8 |
Defline: | (1 of 1) PTHR10795//PTHR10795:SF157//PTHR10795:SF371 - PROPROTEIN CONVERTASE SUBTILISIN/KEXIN // MEMBRANE-BOUND TRANSCRIPTION FACTOR PEPTIDASE, SITE 1 // SUBFAMILY NOT NAMED; Subtilisin-like protease |
Description: | |
Synonyms: | SUB8,g5313.t1 |
Chromosome: | chromosome 5 |
We did not create a plasmid for this gene.
We did not determine any protein-protein interactions for this gene.
Insertion Junction | Mutant Strain | Insertion Junction Feature | Confidence (%) | Genome Version |
---|---|---|---|---|
CLIP2.012085_1 | CLIP2.012085 | CDS | 80 | 6.1 |
CLIP2.016836_1 | CLIP2.016836 | CDS | 80 | 6.1 |
CLIP2.016836_2 | CLIP2.016836 | CDS | 80 | 6.1 |
CLIP2.045205_2 | CLIP2.045205 | CDS | 80 | 6.1 |
CLIP2.058606_1 | CLIP2.058606 | intron | 63 | 6.1 |
CLIP2.060494_1 | CLIP2.060494 | intron | 63 | 6.1 |
CLIP2.077244_1 | CLIP2.077244 | intron | 63 | 6.1 |
CLIP2.077502_1 | CLIP2.077502 | 3'UTR | 80 | 6.1 |
CLIP2.078663_1 | CLIP2.078663 | intron | 63 | 6.1 |
LMJ.RY0402.102165_1 | LMJ.RY0402.102165 | intron | 58 | 5.5 |
LMJ.RY0402.113957_1 | LMJ.RY0402.113957 | intron | 95 | 5.5 |
LMJ.RY0402.113957_2 | LMJ.RY0402.113957 | CDS | 95 | 5.5 |
LMJ.RY0402.151237_1 | LMJ.RY0402.151237 | intron | 73 | 5.5 |
LMJ.RY0402.154208_1 | LMJ.RY0402.154208 | intron | 73 | 5.5 |
LMJ.RY0402.159291_1 | LMJ.RY0402.159291 | intron | 95 | 5.5 |
LMJ.RY0402.175614_1 | LMJ.RY0402.175614 | intron | 73 | 5.5 |
LMJ.RY0402.227429_1 | LMJ.RY0402.227429 | intron | 73 | 5.5 |
LMJ.RY0402.243641_1 | LMJ.RY0402.243641 | intron | 73 | 5.5 |
PFAM: | PF00082 |
PANTHER: | PTHR10795 PTHR10795:SF371 |
KEGG_ec: | EC:3.4.21.62 |
KEGG_orthology: | |
KOG: | |
Gene ontology terms:: | GO:0004252, GO:0006508 |
Best arabidopsis TAIR name: | AT1G04110.1 |
Best arabidopsis TAIR symbol: | SDD1 |
Best arabidopsis TAIR defline: | Subtilase family protein |
Phytozome Locus Page |
Mutants in this gene exhibit a phenotype under the following conditions:
Photosynthesis or light sensitivity, screen 11 of 12 ( 71% confidence (FDR = 0.29)) |
Note: FDR indicates the likelihood that a particular genotype-phenotype relationship is incorrect. Not all mutants in a particular gene show the same phenotype. Please see the mutant pages for each mutant's phenotypes. Complementation is needed to definitively prove a genotype-phenotype link. 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.