FB2026_02 , released June 18, 2026
Allele: Dmel\10381038
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General Information
Symbol
Dmel\10381038
Species
D. melanogaster
Name
FlyBase ID
FBal0189927
Feature type
allele
Associated gene
1038
Associated Insertion(s)
Carried in Construct
Key Links
Allele class
Mutagen
Nature of the Allele
Allele class
Mutagen
X ray
(Coulthard et al., 2005)
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
      External Data
      Interactions
      Show genetic interaction network for Enhancers & Suppressors
      Phenotypic Class
      Enhancer of
      Statement
      Reference

      10381038 is an enhancer of visible phenotype of vg83b27/vg1

      (Coulthard et al., 2005)
      Phenotype Manifest In
      Enhancer of
      Statement
      Reference

      10381038 is an enhancer of haltere phenotype of vg83b27/vg1

      (Coulthard et al., 2005)

      10381038 is an enhancer of wing phenotype of vg83b27/vg1

      (Coulthard et al., 2005)
      Additional Comments
      Genetic Interactions
      Statement
      Reference
      Xenogenetic Interactions
      Statement
      Reference
      Complementation and Rescue Data
      Comments
      Images (0)
      Mutant
      Wild-type
      Stocks (0)
      Notes on Origin
      Discoverer

      Induced on: a vg83b27 chromosome. Selected as: a mutation that disrupts complementation of vg83b27 and vg1.

      (Coulthard et al., 2005)
      Comments
      Comments

      10381038 lacks any visible chromosome rearrangements and does not have a translocation between the second and third chromosomes that contains only heterochromatic breakpoints. Several possibilities remain as to why this line disrupts the complementation of vg83b27 and vg1, including a mutation in a vg modifier, a mutation in the coding region of vg83b27, or a T(1;2) or T(2;4) with heterochromatic breaks.

      (Coulthard et al., 2005)
      External Crossreferences and Linkouts ( 0 )
      Synonyms and Secondary IDs (2)
      Reported As
      Symbol Synonym
      1038
      (Coulthard et al., 2005)
      10381038
      Name Synonyms
      Secondary FlyBase IDs
        References (1)