FB2024_03 , released June 25, 2024
Allele: Dmel\nenyadel
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General Information
Symbol
Dmel\nenyadel
Species
D. melanogaster
Name
FlyBase ID
FBal0345528
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Key Links
Genomic Maps

Allele class
Mutagen
Nature of the Allele
Allele class
Cytology
Description

Deletion of the entire nenya gene.

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

Scer\FRT-mediated recombination between the two progenitor insertions, PBac{WH}minof04927 and PBac{WH}minof01088 has resulted in the deletion of the genomic sequence between them.

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

nenyadel/nenyadel, naryaJJ6/naryaJJ6 females show frequent meiotic chromosome segregation errors, as assessed by X-chromosome non-disjunction; in agreement, meiotic recombination fails to initiate in early pachytene cysts, with few if any DSBs being detected (γH2AV foci). The X-chromosome non-disjunction is fully rescued by the expression of naryaUASp.GFP under the control of Scer\GAL4VP16.nos.UTR. nenyadel/nenyadel, naryaJJ6/+ females, naryaGFP/naryaGFP, nenyadel/+ females and naryaGFP/naryaGFP, nenyadel/nenyadel females do not show significant meiotic chromosome segregation errors, as assessed by X-chromosome non-disjunction.

Xenogenetic Interactions
Statement
Reference
Complementation and Rescue Data
Comments
Images (0)
Mutant
Wild-type
Stocks (0)
Notes on Origin
Discoverer
Comments
Comments

This deletion of nenya may also disrupt the mino gene because nenya is located in the first intron of mino.

External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (1)
Reported As
Symbol Synonym
Name Synonyms
Secondary FlyBase IDs
    References (2)