FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Allele: Dmel\D10
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General Information
Symbol
Dmel\D10
Species
D. melanogaster
Name
FlyBase ID
FBal0059168
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Key Links
Mutagen
Nature of the Allele
Progenitor genotype
Caused by aberration
Cytology
Description

The aberration breakpoint is -21 to -24 kb 3' of the D transcription unit (where 0 indicates the translation start site).

Break in D maps to -21 to -24 where 0 is the translational start of D.

Breakpoint maps 3' to the D transcription unit.

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

Heterozygotes have deletions of anterior and posterior wing structures, including the medial costa, parts of the radius and the alar lobe. D10 mutant wing discs show large number of apoptotic cells.

Lethal when heterozygous with Dr72 or Dr513. The wing phenotype of the dominant alleles is due to ectopic expression of D in the anlage of the hinge in the wing imaginal disc, as can be reproduced using a DScer\UAS.cSa driven by Scer\GAL430A or Scer\GAL4zfh2-MS209.

Lethal in combination with point alleles of D and small deletions which only remove D sequences.

D10/Df(3L)D-5rv6 embryos exhibit intermediate segmentation defects showing segment fusions often in A3 to A7.

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

wing hinge Exhibits a dominant wing hinge phenotype. The nervous system in homozygous embryos appears wild-type.

Images (0)
Mutant
Wild-type
Stocks (0)
Notes on Origin
Discoverer
Comments
Comments

Shows tissue specific loss of D expression in the embryo.

Shows tissue-specific loss of D expression thus is a regulatory mutation.

Associated with a recessive lethal phenotype that maps to 70D1-2.

External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (2)
Reported As
Symbol Synonym
Name Synonyms
Secondary FlyBase IDs
    References (5)