FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Allele: Dmel\rump1
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General Information
Symbol
Dmel\rump1
Species
D. melanogaster
Name
FlyBase ID
FBal0218192
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Key Links
Allele class
Nature of the Allele
Allele class
Progenitor genotype
Cytology
Description

Imprecise excision of the insertion in rumpKG02834, resulting in a deletion starting 426bp upstream and extending 501bp downstream of the original insertion site. This deletion removes the transcription start site, the entire 5'UTR and the first 152 codons of rump.

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
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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
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Modifiers Based on Experimental Evidence ( 0 )
Disease
Interaction
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Comments on Models/Modifiers Based on Experimental Evidence ( 0 )
 
Disease-implicated variant(s)
 
Phenotypic Data
Phenotypic Class
Phenotype Manifest In
Detailed Description
Statement
Reference

10% of rump1 mutant embryos have less than 8 abdominal segments.

Of embryos from rump1 mothers that complete embryogenesis, 11% show abdominal segmentation defects.

Homozygous females show a variable maternal-effect defect in the percentage of progeny that complete embryonic development, ranging from 29% to 65%.

Homozygous males derived from heterozygous parents show reduced fertility; only 10% of males are able to fertilise virgin females within a 10 day period.

Embryos derived from homozygous females show a weak, though significant, segmentation defect, which is variable in its penetrance.

External Data
Interactions
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Additional Comments
Genetic Interactions
Statement
Reference

rump1 mutant embryos carrying a aubQC42/+ mutation display an increase in the number of embryos that develop less than 8 abdominal segments.

rump1 mutant embryos carrying a nosBN, nos+1+3.T:MS2\MCP.BS/nosBN mutation display an increase in the number of embryos that develop less than 8 abdominal segments.

rump1 mutant embryos carrying an aubQC42/+ mutation, and the mutation nosBN, nos+1+3.T:MS2\MCP.BS/nosBN , display an increase in the number of embryos that develop less than 8 abdominal segments.

54% of embryos from lost1, rump1 mothers fail to develop.

Abdominal segmentation defects are more prevalent among surviving lost1, rump1 progeny (18%) than for either lost1 (7%) or rump1 (11%).

Embryos from lost1, rump1 mothers have significantly fewer pole cells than wild type.

The frequency and severity of abdominal segmentation defects in embryos derived from rump1 homozygous females is increased by one copy of nosBN. Abdominal segments 4 and 5 are most frequently affected.

rump1 enhances in a dose-dependent manner the abdominal segmentation defects seen in tudtux46/+ embryos, with 44% of embryos showing segmental deletions and fusions in the absence of rump+. The 4th and 5th abdominal segments are most often affected.

The ability of nosnos.+2.Hsp83 to rescue abdominal segmentation of nosBN embryos is severely compromised in a rump1/Df(3R)by416 background; more than 90% of the embryos develop fewer than 4 abdominal segments.

Xenogenetic Interactions
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Reference
Complementation and Rescue Data
Rescued by
Comments
Images (0)
Mutant
Wild-type
Stocks (2)
Notes on Origin
Discoverer
External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (2)
Reported As
Name Synonyms
Secondary FlyBase IDs
    References (5)