FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Allele: Dmel\dind2870
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General Information
Symbol
Dmel\dind2870
Species
D. melanogaster
Name
FlyBase ID
FBal0344727
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Key Links
Genomic Maps

Allele class
Nature of the Allele
Allele class
Progenitor genotype
Cytology
Description

Nature of lesion is a revision of data reported in FBrf0240471.

Amino acid replacement: Q274term.

Mutations Mapped to the Genome
Curation Data
Type
Location
Additional Notes
References
Nucleotide change:

C18676088T

Amino acid change:

Q274term | dind-PA

Reported amino acid change:

Q274term

Comment:

Site of nucleotide substitution in mutant inferred by FlyBase curator based on reported amino acid change.

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

dind2870/Df(3R)BX5 transheterozygous third instar larvae present smaller brains with reduced numbers of dividing cells (decrease in BrdU labelling) that show a metaphase delay (increase in mitotic index but decrease in proportion of cells in anaphase or telophase), as compared to controls. Mitotic brain cells exhibit defects in chromosome number and morphology that are virtually absent in controls: frequent hyperploidy and polyploidy, and less frequent chromosome endo-replication; frequent unevenly or over-condensed chromosomes; and several types of chromosome aberrations, such as chromatid deletions, isochromatid breaks, and complex rearrangements. Mitotic brain cells also exhibit poor chromosome alignment, distorted spindles and defective centrosome number, as compared to controls.

Likewise, spermatogonia in dind2870/Df(3R)BX5 transheterozygous third instar larvae are much frequently in metaphase than controls and these metaphases display frequent defects that are virtually absent in controls: significantly longer spindles; irregular number of centrosomes; frequent unevenly or over-condensed chromosomes; and frequent hyperploidy/polyploidy and chromosome aberrations. Mature primary spermatocytes also exhibit some defects that are virtually absent in controls: centriole integrity defects; highly frequent detachment of asters from the chromosome-attached spindle; and frequent mis-orientation between the two daughter nuclei and the spindle axis at telophase. Unlike controls, onion stage spermatids in dind2870/Df(3R)BX5 transheterozygous third instar larvae show abnormally sized nuclei and Nebenkern, and the association between these two structures is generally lost, but abnormal spermatids are able to differentiate and produce sperm with long axonemes.

External Data
Interactions
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Phenotypic Class
Phenotype Manifest In
Additional Comments
Genetic Interactions
Statement
Reference
Xenogenetic Interactions
Statement
Reference
Complementation and Rescue Data
Images (0)
Mutant
Wild-type
Stocks (0)
Notes on Origin
Discoverer
External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (2)
Reported As
Name Synonyms
Secondary FlyBase IDs
    References (3)