Common name: | BLD12,SAS6 |
Defline: | (1 of 1) K16487 - spindle assembly abnormal protein 6 (SAS-6, SASS6); Bald 12 |
Description: | Found in basal body proteome as BLD12; Basal body cartwheel protein that establishes the 9-fold symmetry of the centriole; Mutant is deficient in establishing 9-fold symetry and lacks flagella (bald phenotype) when grown under normal conditions; NCBI accession number BAF94334; Related to SAS-6 in humans |
Synonyms: | Cre12.g516950.t1.1,SAS6,g12750.t1 |
Chromosome: | chromosome 12 |
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 |
---|---|---|---|---|
CLIP2.012104_1 | CLIP2.012104 | CDS | 80 | 6.1 |
CLIP2.021015_1 | CLIP2.021015 | intron | 80 | 6.1 |
CLIP2.021015_2 | CLIP2.021015 | intron | 80 | 6.1 |
CLIP2.026879_3 | CLIP2.026879 | intron | 80 | 6.1 |
CLIP2.051394_1 | CLIP2.051394 | intron | 80 | 6.1 |
CLIP2.051394_2 | CLIP2.051394 | intron | 80 | 6.1 |
CLIP2.051450_1 | CLIP2.051450 | CDS | 80 | 6.1 |
CLIP2.055673_1 | CLIP2.055673 | intron | 80 | 6.1 |
CLIP2.065229_1 | CLIP2.065229 | 3'UTR | 80 | 6.1 |
CLIP2.065229_2 | CLIP2.065229 | 3'UTR | 80 | 6.1 |
CLIP2.069211_1 | CLIP2.069211 | 3'UTR | 80 | 6.1 |
CLIP2.069211_2 | CLIP2.069211 | 3'UTR | 80 | 6.1 |
LMJ.RY0402.120949_1 | LMJ.RY0402.120949 | CDS/intron | 73 | 5.5 |
LMJ.RY0402.145229_1 | LMJ.RY0402.145229 | CDS | 95 | 5.5 |
LMJ.RY0402.145229_2 | LMJ.RY0402.145229 | CDS | 95 | 5.5 |
LMJ.RY0402.152301_1 | LMJ.RY0402.152301 | intron | 73 | 5.5 |
LMJ.RY0402.204747_1 | LMJ.RY0402.204747 | CDS | 73 | 5.5 |
PFAM: | PF16531 |
PANTHER: | PTHR18937 PTHR18937:SF223 |
KEGG_ec: | |
KEGG_orthology: | K16487 |
KOG: | KOG1850 |
Gene ontology terms:: | |
Best arabidopsis TAIR name: | |
Best arabidopsis TAIR symbol: | |
Best arabidopsis TAIR defline: | |
Phytozome Locus Page |
Mutants in this gene exhibit a phenotype under the following conditions:
Methyl methanesulfonate, screen 4 of 4 ( 77% confidence (FDR = 0.23)) |
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.