FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Allele: Dmel\ranshie00091
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General Information
Symbol
Dmel\ranshie00091
Species
D. melanogaster
Name
FlyBase ID
FBal0160760
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Key Links
Genomic Maps

Nature of the Allele
Progenitor genotype
Associated Insertion(s)
Cytology
Description

Insertion within intron 1, approximately 146bp downstream of the translational initiation site.

Allele components
Component
Use(s)
Inserted element
Mutations Mapped to the Genome
Curation Data
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 males are viable, fertile and indistinguishable from wild type.

Homozygous females fail to lay eggs. All egg chambers of homozygous females contain 16 germline cells, but they lack karyosomes. The nuclei of all the germline cells contain endoreplicated DNA that is typically seen in nurse cells. Spectrosome/fusome development appears indistinguishable from wild type in homozygous females. Meiosis is not restricted to a single cells in mutant germaria, as assessed by the presence of synaptonemal complexes in two adjacent cells within germarial region 3. In mutant cysts containing a single cell with synaptonemal complex, centrosomes accumulate within the cell containing the synaptonemal complex (as occurs in wild type), however, they are not detected within the posterior of the cell but are randomly placed within the cytoplasm.

External Data
Interactions
Show genetic interaction network for Enhancers & Suppressors
Phenotypic Class
Phenotype Manifest In
Additional Comments
Genetic Interactions
Statement
Reference
Xenogenetic Interactions
Statement
Reference
Complementation and Rescue Data
Comments
Images (0)
Mutant
Wild-type
Stocks (1)
Notes on Origin
Discoverer

FlyBase curator comment: The "Df(3R)ranshi[1]" chromosome and the allele called "ranshi[1]" in FBrf0210119 (ranshie00091 in FlyBase) are two separate mutations. The ranshie00091 allele is caused by the PBac{RB}ranshie00091 insertion. The Df(3R)ranshi1 chromosome is a different mutation derived by recombination between the Scer\FRT sites in PBac{RB}ranshie00091 and P{XP}d11678.

Comments
Comments

Precise excision of the progenitor insertion reverts the mutant phenotype.

External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (3)
Reported As
Symbol Synonym
CG9793e00091
ranshie00091
Name Synonyms
Secondary FlyBase IDs
    References (3)