Gene: Cre17.g741950 (Genome version: v5.5)

Overview

Common name:BBS1
Defline:Bardet-Biedl syndrome-1 associated protein
Description:Similar to Bardet-Biedl syndrome 1
Synonyms:g17944.t1,BBS1
Chromosome:chromosome_17

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 Orientation Insertion Junction Feature Confidence (%)
LMJ.RY0402.048677_1 LMJ.RY0402.048677 antisense CDS 73
LMJ.RY0402.059939_1 LMJ.RY0402.059939 antisense intron 73
LMJ.RY0402.083580_1 LMJ.RY0402.083580 sense CDS 58
LMJ.RY0402.083580_2 LMJ.RY0402.083580 antisense intron 73
LMJ.RY0402.089152_1 LMJ.RY0402.089152 antisense intron 73
LMJ.RY0402.134921_1 LMJ.RY0402.134921 sense intron 73
LMJ.RY0402.144285_2 LMJ.RY0402.144285 antisense intron 73
LMJ.RY0402.157822_1 LMJ.RY0402.157822 sense intron 95
LMJ.RY0402.157822_2 LMJ.RY0402.157822 sense intron 95
LMJ.RY0402.173395_1 LMJ.RY0402.173395 sense intron 58
LMJ.RY0402.180117_3 LMJ.RY0402.180117 antisense CDS 73
LMJ.RY0402.186225_2 LMJ.RY0402.186225 sense intron 95
LMJ.RY0402.186225_3 LMJ.RY0402.186225 sense CDS 95
LMJ.RY0402.193332_1 LMJ.RY0402.193332 antisense intron 95
LMJ.RY0402.208040_2 LMJ.RY0402.208040 sense 3'UTR 73
LMJ.RY0402.215489_1 LMJ.RY0402.215489 sense 3'UTR 95
LMJ.RY0402.215489_2 LMJ.RY0402.215489 sense 3'UTR 95
LMJ.RY0402.229466_1 LMJ.RY0402.229466 sense intron 95
LMJ.RY0402.229466_2 LMJ.RY0402.229466 sense intron 95
LMJ.RY0402.234079_1 LMJ.RY0402.234079 sense intron 95
LMJ.RY0402.234079_2 LMJ.RY0402.234079 sense intron 95

Gene Annotations

PFAM:
PANTHER: PTHR20870
KEGG_ec:
KEGG_orthology:
KOG:
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:

Flagella, screen 3 of 6 ( 72% confidence (FDR = 0.28))
Predator, screen 10 of 11 ( 95% confidence (FDR = 0.048))

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.