FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Allele: Dmel\odd5
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General Information
Symbol
Dmel\odd5
Species
D. melanogaster
Name
FlyBase ID
FBal0013225
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Also Known As
oddIIID36, oddIIId
Key Links
Nature of the Allele
Progenitor genotype
Cytology
Description
Mutations Mapped to the Genome
Curation Data
Type
Location
Additional Notes
References
Variant Molecular Consequences
Associated Sequence Data
DNA sequence
Protein sequence
 
Expression Data
Reporter Expression
Additional Information
Statement
Reference
 
Marker for
Reflects expression of
Reporter construct used in assay
Human Disease Associations
Disease Ontology (DO) Annotations
Models Based on Experimental Evidence ( 0 )
Disease
Evidence
References
Modifiers Based on Experimental Evidence ( 0 )
Disease
Interaction
References
Comments on Models/Modifiers Based on Experimental Evidence ( 0 )
 
Disease-implicated variant(s)
 
Phenotypic Data
Phenotypic Class
Phenotype Manifest In
Detailed Description
Statement
Reference

Stage 12 odd5 embryos exhibit a mirro-image duplication of the wg expression domain and a concurrent replication of SOP cells within and adjacent to this ectopic domain.

Homozygous mutant clones in the leg can cause fusions between tarsal segments t1-t5.

The maxillary lobe is fused with a reduced labial lobe in mutant embryos.

Pattern defects in the anterior region of odd-numbered segments leading to the deletion of denticle belts A1, A3, A5 and A7. The overall muscle pattern is severely disturbed. The number of apodeme rows ventrally and laterally is reduced by half and their spatial distribution is irregular.

Does not interact with RpII140wimp maternal effect.

Strong allele. Odd-numbered denticle belts are deleted or reduced to one or two duplicated anterior rows in homozygous larvae. The phenotype of eve1 odd5 double homozygotes at 29oC is not an additive effect of the two mutations; the double mutant has 7 or 8 partial denticle belts, each with an apparent polarity reversal. The phenotype of odd5 prd10 double homozygotes is more limited than simple additivity of the two phenotypes. The odd5 phenotype is largely suppressed by en57 in double homozygotes.

Odd numbered denticle bands missing.

Partial deletion of odd denticle bands.

embryonic lethal strong allele

External Data
Interactions
Show genetic interaction network for Enhancers & Suppressors
Phenotypic Class
Phenotype Manifest In
Additional Comments
Genetic Interactions
Statement
Reference
Xenogenetic Interactions
Statement
Reference
Complementation and Rescue Data
Comments
Images (0)
Mutant
Wild-type
Stocks (7)
Notes on Origin
Discoverer
Comments
Comments

prd RNA expression has been studied in odd5 eve1 double mutant embryos.

External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (7)
References (30)