FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Allele: Dmel\l(1)16Fm23437
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General Information
Symbol
Dmel\l(1)16Fm23437
Species
D. melanogaster
Name
FlyBase ID
FBal0095334
Feature type
allele
Associated gene
l(1)16Fm
Associated Insertion(s)
Carried in Construct
Key Links
Allele class
Mutagen
Nature of the Allele
Allele class
Mutagen
X ray
(Prado et al., 1999)
Progenitor genotype
Cytology
Description

2kb deletion, located 100bp upstream of the wupA transcription start site.

(Prado et al., 1999)
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
      Phenotype Manifest In
      Additional Comments
      Genetic Interactions
      Statement
      Reference

      l(1)16Fm23437/l(1)16Fm23437 embryos show remnants of somatic muscles with randomly-spaced putative Z discs.

      (Marin et al., 2004)

      The '23437' chromosome (in which l(1)16Fm and l(1)16Fe are affected) fully complements wupAhdp-2. The '23437' chromosome fails to complement wupAhdp-3, resulting in severe muscle defects. The '23437' chromosome fails to complement the semi-dominant lethality of wupA8384 or wupA24597. Embryos homozygous for the '23437' chromosome have hypodermal and neural phenotypes. l(1)16Fk26174 fails to complement the '23437' chromosome (in which l(1)16Fm and l(1)16Fe are affected).

      (Prado et al., 1999)
      Xenogenetic Interactions
      Statement
      Reference
      Complementation and Rescue Data
      Fails to complement

      l(1)16Fm5374

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

      Separable from: l(1)16Fm23437. Mutation affecting both l(1)16Fe and l(1)16Fm.

      (Prado et al., 1999)
      External Crossreferences and Linkouts ( 0 )
      Synonyms and Secondary IDs (2)
      Reported As
      Symbol Synonym
      23437
      (Prado et al., 1999)
      l(1)16Fm23437
      Name Synonyms
      Secondary FlyBase IDs
        References (2)