Gene: Cre12.g516950

Overview

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

Protein Localization

We did not create a plasmid for this gene.

Protein-Protein Interactions

We did not determine any protein-protein interactions for this gene.

Mutant Strains

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

Gene Annotations

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

Phenotypes

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.