FB2026_02 , released June 18, 2026
Allele: Dmel\tsl604
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General Information
Symbol
Dmel\tsl604
Species
D. melanogaster
Name
FlyBase ID
FBal0035848
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
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Allele class
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Allele class
Progenitor genotype
Associated Insertion(s)
Cytology
Description

P-element insertion between the tsl and Caki transcription units.

Mutations Mapped to the Genome
Curation Data
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
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Models Based on Experimental Evidence ( 0 )
Disease
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Modifiers Based on Experimental Evidence ( 0 )
Disease
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Comments on Models/Modifiers Based on Experimental Evidence ( 0 )
 
Disease-implicated variant(s)
 
Phenotypic Data
Phenotypic Class
Phenotype Manifest In
Detailed Description
Statement
Reference

Pupariation is delayed in tsl604/Df(3R)cakiX-313 mutant larvae.

Pupariation is delayed in homozygous tsl604 mutant larvae.

tsl604 mutant embryos exhibit anterior terminal structure defects. The dorsal bridge is absent in 100% of embryos.

Lack anterior most head structures and all structures posterior to abdominal segment 7. Females carrying one copy of the P{hsp-tsl} construct produce embryos that display a tor phenotype. Some embryos are almost wild type showing only weak rescue of head defects. Injection of tslco51b transcripts, synthesised in vitro from tsl cDNA, into the posterior region of early embryos causes some posterior rescue in larvae.

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Xenogenetic Interactions
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Complementation and Rescue Data
Partially rescued by
Comments

Expression of tslScer\UAS.cSa under the control of Scer\GAL4slbo.2.6 rescues the anterior terminal structure defects seen in tsl604 mutant embryos, with 100% of embryos having a dorsal bridge. However, many of the embryos have head involution defects, meaning that only embryos with normal head involution could be examined. The posterior phenotype is also rescued, but not in all embryos.

Expression of tslScer\UAS.cSa under the control of Scer\GAL4tsl.G rescues the anterior and posterior terminal structure defects seen in tsl604 mutant embryos, with 100% of embryos having a dorsal bridge.

Expression of tslScer\UAS.cSa under the control of Scer\GAL4tsl.F rescues the anterior and terminal structure defects seen in tsl604 mutant embryos, with 100% of embryos having a dorsal bridge. The posterior phenotypes are not rescued.

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Mutant
Wild-type
Stocks (1)
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Synonyms and Secondary IDs (1)
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    References (7)