FB2024_03 , released June 25, 2024
Allele: Dmel\btdXA
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General Information
Symbol
Dmel\btdXA
Species
D. melanogaster
Name
FlyBase ID
FBal0030657
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Key Links
Genomic Maps

Mutagen
    Nature of the Allele
    Mutagen
    Progenitor genotype
    Cytology
    Description

    Construct: Amino acid replacement: Q70@.

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

    C9694881T

    Amino acid change:

    Q70term | btd-PA

    Reported amino acid change:

    Q70term

    Comment:

    Site of nucleotide substitution in mutant inferred by FlyBase based on reported amino acid change.

    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

    Type II neuroblasts in homozygous clones in the larval brain maintain a type II neuroblast marker expression profile. They appear to generate non-functional ase[-] immature intermediate neural progenitors that likely adopt an identity of ganglion mother cells normally found in the type I neuroblast lineage.

    Homozygous embryos fail to form a cephalic furrow. The ventral furrow and proctodeal invagination form normally. No signs of initiator cell activity are seen between the beginning of cycle 14 and stage 7.

    The lateral pentascolopidial chordotonal organs (lch5) in the abdominal segments contain an average of 3 to 4 scolopidia in mutant embryos.

    A weak allele of btd. Mandibular, intercalary and antennal segments absent.

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

    btdXA ; bratunspecified double mutant clones in the larval brain do not lead to supernumerary neuroblast formation.

    Xenogenetic Interactions
    Statement
    Reference
    Complementation and Rescue Data
    Rescued by
    Partially rescued by

    btdXA is partially rescued by btd+t10.5

    Not rescued by
    Comments

    The reduction in the number of scolopidia in lch5 in btdXG embryos is partially rescued by btd+t10.5.

    Images (0)
    Mutant
    Wild-type
    Stocks (1)
    Notes on Origin
    Discoverer
    External Crossreferences and Linkouts ( 0 )
    Synonyms and Secondary IDs (3)
    Reported As
    Name Synonyms
    Secondary FlyBase IDs
      References (14)