FB2025_01 , released February 20, 2025
Allele: Dmel\Xrcc2CC
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General Information
Symbol
Dmel\Xrcc2CC
Species
D. melanogaster
Name
FlyBase ID
FBal0359105
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Key Links
Genomic Maps

Mutagen
Nature of the Allele
Progenitor genotype
Cytology
Description

Deletion in Xrcc2; coordinates X:18500252..18501142 , release 6 genome.

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

The deletion starts downstream of the AUG and removes most of Xrcc2.

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

Xrcc2CC homozygous adults don't exhibit any apparent phenotypes and females lay eggs of normal appearance with respect to dorso-ventral patterning when compared to controls.

Xrcc2CC homozygous female flies exhibit a mild increase in the frequency of X-chromosome nondisjunction while their ability to generate recombinant chromosomes is only slightly compromised when compared to controls.

Xrcc2CC homozygotes exhibit a high sensitivity to the DNA damaging agents (complete or near complete lethality upon Methyl methanesulfonate or Hydroxyurea treatment, and a decrease in survival in response to Camptothecin or ionizing radiation exposure) when compared to controls.

Xrcc2CC homozygous third instar larvae exhibit an increase in chromosomal aberrations in larval neuroblasts compared to controls. Also after ionizing radiation exposure the chromosomal defects and the DNA damage response (phosphorylated histone variant H2AX staining) persist much longer although the damage to chromosomes is similar compared to controls.

External Data
Interactions
Show genetic interaction network for Enhancers & Suppressors
Phenotypic Class
Phenotype Manifest In
Enhancer of
Statement
Reference
NOT Enhancer of
Statement
Reference
NOT Suppressor of
Statement
Reference

Xrcc2CC/Xrcc2CC is a non-suppressor of dorsal appendage phenotype of spn-A093A/spn-A1

Other
Additional Comments
Genetic Interactions
Statement
Reference

Xrcc2CC homozygous females in the heterozygous background of CycGHR7, spn-A093A, spn-A1, spn-B2 or spn-BBU lay eggs with defective dorsal appendages (fused, narrowly spaced, branched or shortened) when compared to controls.

Xenogenetic Interactions
Statement
Reference
Complementation and Rescue Data
Rescued by
Comments
Images (0)
Mutant
Wild-type
Stocks (1)
Notes on Origin
Discoverer
External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (2)
Reported As
Symbol Synonym
Name Synonyms
Secondary FlyBase IDs
    References (2)