FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Allele: Dmel\thrk01302
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General Information
Symbol
Dmel\thrk01302
Species
D. melanogaster
Name
FlyBase ID
FBal0095176
Feature type
allele
Associated gene
Dmel\thr
Associated Insertion(s)
Carried in Construct
Key Links
Allele class
Mutagen
    Nature of the Allele
    Allele class
    Mutagen
    Progenitor genotype
    Cytology
    Description
    Mutations Mapped to the Genome
    Curation Data
    Type
    Location
    Additional Notes
    References
    Variant Molecular Consequences
    Associated Sequence Data
    DDBJ / EMBL / GenBank
    DNA sequence
    Protein sequence
     
    UniProtKB/Swiss-Prot
      UniProtKB/TrEMBL
        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

        Malpighian tubules are short with fewer but larger cells than normal. The hindgut and foregut are short. Midgut constrictions do not form. Head involution is incomplete, tracheae are abnormal and there are holes in the epidermis.

        (Liu et al., 1999)
        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
        Fails to complement

        thr1

        (Liu et al., 1999)
        Comments
        Images (0)
        Mutant
        Wild-type
        Stocks (0)
        Notes on Origin
        Discoverer

        thrk01302 was identified in the 'l(2)k01302' line. A deficiency uncovering the site of the P{lacW}tkvk01302 insertion complements the 'l(2)k01302' chromosome for lethality and does not produce embryos with the defects characteristic of the homozygous 'l(2)k01302' line. This suggests that the thrk01302 mutation (representing the lethality and embryonic defects) is not caused by the P{lacW}l(2)k01302k01302 insertion.

        (Liu et al., 1999)
        External Crossreferences and Linkouts ( 0 )
        Synonyms and Secondary IDs (2)
        Reported As
        Symbol Synonym
        k01302
        (Liu et al., 1999)
        thrk01302
        Name Synonyms
        Secondary FlyBase IDs
          References (1)