FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Allele: Dmel\galla-1Δ182
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General Information
Symbol
Dmel\galla-1Δ182
Species
D. melanogaster
Name
FlyBase ID
FBal0317013
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Key Links
Genomic Maps

Nature of the Allele
Cytology
Description

Imprecise excision of P{EPgy2}CG30152EY01427 has resulted in a 968bp deletion that removes almost the entire galla-1 coding sequence

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

Inferred boundaries of a 968 bp deletion resulting from the imprecise excision of P{EPgy2}galla-1EY01427 that extends downstream from the P element insertion site and removes most of galla-1. The deletion is reported to remove the coding sequence from amino acid 38.

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

Homozygous galla-1Δ182 mutants show temperature-dependent lethality. While about 50% of the mutants die during development at 25[o]C, 95% animals die at 29[o]C. At 29[o]C, more than 70% of the mutants die during embryonic stages and the rest die throughout larval and pupal stages.

galla-1Δ182 mutant embryos show defects in chromosome segregation. They exhibit patchy areas that have centrosomes but not chromosomes. galla-1Δ182 mutant early embryos show large areas of defective divisions such as chromosome bridges and abnormal positioning of centrosomes due to incomplete segregation.

galla-1Δ182/Df(2R)Exel6070 mutant embryos show consistent chromosome segregation defect phenotypes such as chromosome bridges, ectopic centrosomes and abnormal patterns of spindle microtubules.

External Data
Interactions
Show genetic interaction network for Enhancers & Suppressors
Phenotypic Class
Enhanced by
Statement
Reference
Suppressor of
Phenotype Manifest In
Suppressor of
Statement
Reference
Additional Comments
Genetic Interactions
Statement
Reference

One copy of galla-1Δ182 does not obviously suppress the small and rough eye phenotype seen when crbintra.Scer\UAS.T:Hsap\MYC is expressed under the control of Scer\GAL4GMR.PU. Homozygous galla-1Δ182 results in significant rescue of the eye phenotype.

The partial lethality seen in galla-1Δ182 mutants is considerably enhanced by one copy of galla-2Δ203.

Xenogenetic Interactions
Statement
Reference
Complementation and Rescue Data
Comments
Images (0)
Mutant
Wild-type
Stocks (0)
Notes on Origin
Discoverer
External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (1)
Reported As
Symbol Synonym
galla-1Δ182
Name Synonyms
Secondary FlyBase IDs
    References (1)