FB2025_05 , released December 11, 2025
Allele: Dmel\wusG0162
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General Information
Symbol
Dmel\wusG0162
Species
D. melanogaster
Name
FlyBase ID
FBal0133957
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Also Known As
wurstl(1)G0162
Key Links
Genomic Maps

Nature of the Allele
Progenitor genotype
Associated Insertion(s)
Cytology
Description
Allele components
Component
Use(s)
Inserted element
Encoded product / tool
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
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

Stage 17 wusG0162 mutant embryos show defects in the transition from luminal liquid-clearance to air-filled airways. Tube size defects and defective airway protein clearance are also seen. No air-filling defects are observed in wusG0162 heterozygotes.

Hemizygous stage 16 embryos show an increase in tracheal length and diameter compared to wild type, resulting in curved tracheal branches.

Secretion of extracellular matrix (ECM) into the lumen of the tracheal tubes occurs normally in mutant embryos, but its organisation into the central chitin cylinder and the gap region fails to occur (an accumulation of chitin fibres is seen in the mutant tube lumens). In contrast to wild type, lumen clearance (the degradation of chitinous ECM and removal of protein and liquid) does not occur in late stage 17 mutant embryos, and as a consequence, gas filling fails to occur. The mutant animals die as late embryos.

The apical cell membranes of tracheal cells are enlarged in mutant embryos, being disorganised and containing folds that are likely to be due to extra-membrane material.

Endocytosis is defective in mutant epidermal cells (as seen by a reduction in uptake of a biotin tracer).

External Data
Interactions
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Phenotypic Class
Phenotype Manifest In
Additional Comments
Genetic Interactions
Statement
Reference

Transheterozygous wusG0162 crb2 stage 17 embryos show defects in in the transition from luminal liquid-clearance to air-filled airways.

Transheterozygous wusG0162 crbj1B5 stage 17 embryos show defects in in the transition from luminal liquid-clearance to air-filled airways.

Xenogenetic Interactions
Statement
Reference
Complementation and Rescue Data
Comments
Images (0)
Mutant
Wild-type
Stocks (0)
Notes on Origin
Discoverer
External Crossreferences and Linkouts ( 1 )
Crossreferences
GenBank Nucleotide - A collection of sequences from several sources, including GenBank, RefSeq, TPA, and PDB.
Synonyms and Secondary IDs (4)
Reported As
Symbol Synonym
Name Synonyms
Secondary FlyBase IDs
    References (5)