Gene: Cre01.g029150 (Genome version: v5.5)

Overview

Common name:DAU1,ODA7
Defline:Outer row dynein assembly protein, predominantly cytoplasmic
Description:Outer row dynein assembly protein, ODA7 [PMID: 17194703], predominantly cytoplasmic. Identified by comparative genomics as being present only in organisms having motile (MOT) cilia. Ortholog of human LRRC50, mutations in which can result in primary cil
Synonyms:g664.t1,Cre01.g029150.t1.1,ODA7
Chromosome:chromosome_1

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.RY0402.038561_1 LMJ.RY0402.038561 sense CDS 73
LMJ.RY0402.079975_1 LMJ.RY0402.079975 antisense 3'UTR 58
LMJ.RY0402.082679_1 LMJ.RY0402.082679 antisense 5'UTR 73
LMJ.RY0402.105230_1 LMJ.RY0402.105230 sense CDS 95
LMJ.RY0402.105230_2 LMJ.RY0402.105230 sense CDS 95
LMJ.RY0402.174383_2 LMJ.RY0402.174383 sense CDS 73
LMJ.RY0402.204862_1 LMJ.RY0402.204862 antisense CDS 95
LMJ.RY0402.204862_2 LMJ.RY0402.204862 antisense CDS 95
LMJ.RY0402.216249_1 LMJ.RY0402.216249 sense CDS 58
LMJ.RY0402.220811_1 LMJ.RY0402.220811 antisense CDS 73
LMJ.RY0402.231726_1 LMJ.RY0402.231726 antisense intron 58
LMJ.RY0402.236410_1 LMJ.RY0402.236410 sense CDS 95
LMJ.RY0402.236410_2 LMJ.RY0402.236410 sense CDS 95
LMJ.RY0402.240811_1 LMJ.RY0402.240811 antisense intron 58

Gene Annotations

PFAM:PF00560
PANTHER: PTHR10588:SF7 PTHR10588
KEGG_ec:
KEGG_orthology:
KOG:KOG2739
Gene ontology terms::GO:0005515
Best arabidopsis TAIR name:AT5G22320.1
Best arabidopsis TAIR symbol:
Best arabidopsis TAIR defline:Leucine-rich repeat (LRR) family protein
Phytozome Locus Page

Phenotypes

Mutants in this gene exhibit a phenotype under the following conditions:

Flagella, screen 3 of 6 ( 79% confidence (FDR = 0.21))
Zeocin, screen 4 of 5 ( 96% confidence (FDR = 0.035))

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.