FB2024_03 , released June 25, 2024
Allele: Dmel\α-SpecE2-26
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General Information
Symbol
Dmel\α-SpecE2-26
Species
D. melanogaster
Name
FlyBase ID
FBal0096862
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Also Known As
α-spectrinE2-26
Key Links
Allele class
Nature of the Allele
Allele class
Progenitor genotype
Cytology
Description

Nucleotide substitution: A250T.

Amino acid replacement: ?84term.

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

Homozygous embryos show no obvious axonal phenotypes under standard temperature conditions. If the embryos are allowed to develop at 4oC for 1 day, a fused commissure phenotype develops.

Mutant embryos show a clear fusion of commissures and frequent disruption of longitudinal connectives. Midline glial cells are either reduce in number or fail to properly migrate in between anterior and posterior commissures. General embryonic morphology is relatively normal, though the PNS shows a slight reduction in sensory neurons and defects in the trajectories of motoneurons.

External Data
Interactions
Show genetic interaction network for Enhancers & Suppressors
Phenotypic Class
Phenotype Manifest In
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

Embryos homozygous for the original α-SpecE2-26 chromosome (which contained background mutations) have an axonal phenotype (partially fused commissures), but α-SpecE2-26 homozygotes in which the background mutations have been removed from the chromosome show no axonal phenotypes under standard temperature conditions.

Separable from: Background lethal mutations.

External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (5)
Reported As
Symbol Synonym
kloE2-026
α-SpecE2-26
α-spectrinE2-26
α-spectrine2-26
Name Synonyms
Secondary FlyBase IDs
    References (4)