FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Allele: Dmel\rhea2
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General Information
Symbol
Dmel\rhea2
Species
D. melanogaster
Name
FlyBase ID
FBal0062488
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Key Links
Genomic Maps

Allele class
Mutagen
    Nature of the Allele
    Allele class
    Mutagen
    Progenitor genotype
    Cytology
    Description

    A frameshift occurs after codon 1279; the resulting reading frame terminates after specifying 31 out of frame amino acids.

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

    Approximate location of small deletion after residue 1279 that leads to a frameshift and early translation termination. The resulting reading frame terminates after specifying 31 out of frame amino acids.

    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

    Adult-generated rhea2 homozygous mutant intestinal stem cell clones have reduced maintenance 7 days and 14 days after clone induction compared to control clones; remaining clones contain fewer cells by day 14.

    rhea2 dorsal branch terminal cell clones in third instar larvae show a loss of branches and increase in lumen number.

    Homozygous follicle cell clones that are not situated at the posterior of the egg chamber cause mislocalisation of the oocyte in 50% of egg chambers, while homozygous follicle cell clones at the posterior of the egg chamber do not cause oocyte mispositioning. In egg chambers where there is mislocalisation of the oocyte, the oocyte is in contact with the mutant follicle cell clone in 95% of cases.

    Embryos maternally and zygotically homozygous for rhea2 exhibit a failure of germ-band retraction and a more severe muscle detachment phenotype than embryos zygotically but not maternally homozygous. In rhea2 mutant embryos the gastric caecae fail to split from two initial evaginations into four slender tubes, the midgut does not elongate and the proventriculus does not form properly (n>30).

    External Data
    Interactions
    Show genetic interaction network for Enhancers & Suppressors
    Phenotypic Class
    Enhancer of
    Statement
    Reference

    rhea[+]/rhea2 is an enhancer of visible | recessive phenotype of mys8

    rhea[+]/rhea2 is an enhancer of visible | recessive phenotype of mysb9

    Phenotype Manifest In
    Enhancer of
    Statement
    Reference

    rhea[+]/rhea2 is an enhancer of wing phenotype of mys8

    rhea[+]/rhea2 is an enhancer of wing phenotype of mysb9

    Additional Comments
    Genetic Interactions
    Statement
    Reference

    Shows a strong genetic interaction with mysb9; the frequency of wing blisters and the penetrance of the wings held-out phenotype in mysb9 single hemizygotes is increased from 1-2% to 50-60%, and from 60-80% to 90% respectively, if they are also heterozygous for rhea2.

    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 (2)
    Reported As
    Name Synonyms
    Secondary FlyBase IDs
      References (7)