FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Allele: Dmel\wol2
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General Information
Symbol
Dmel\wol2
Species
D. melanogaster
Name
FlyBase ID
FBal0154349
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Key Links
Genomic Maps

Allele class
Nature of the Allele
Allele class
Progenitor genotype
Cytology
Description

Nucleotide substitution: G?A.

Amino acid replacement: W316term.

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

G8301571A

Reported nucleotide change:

G?A

Amino acid change:

W316term | wol-PA

Reported amino acid change:

W316term

Comment:

G to A nucleotide change at the second or third position of the Trp codon leads to a nonsense mutation (exact site of mutation unspecified). 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

Mutant embryos have defects in germband extension.

Homozygous or wol2/Df(2L)BSC111 larvae hatch and have a wild type cuticle by light microscopy. They eventually die after one moult without displaying any obvious phenotype.

The cuticle of wol2 larvae is less compact, as fissures loosen the procuticle without, grossly disrupting chitin organization. In addition to this defect, the procuticle of larvae lacking maternal wol derived from wol2 germline clones harbors electron-dense material.

Embryos derived from females carrying homozygous germline clones have segmentation defects in the posterior half of the embryo, and a curled-up phenotype resulting from defects in germband elongation and retraction.

Embryos that lack maternal wol function (derived from females carrying homozygous germ line clones) show deletions of alternating abdominal ventral denticle belts, and have a short head and Filzkorper. Embryos that lack both maternal and zygotic wol function (derived from females carrying homozygous germ line clones mated to mutant males) have more severe defects and cuticle holes.

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

gnyf04215, wol2 double mutant embryos fully develop into larvae that hatch and die at the second instar.

Xenogenetic Interactions
Statement
Reference
Complementation and Rescue Data
Comments
Images (0)
Mutant
Wild-type
Stocks (0)
Notes on Origin
Discoverer
External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (3)
Reported As
Name Synonyms
Secondary FlyBase IDs
    References (5)