FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Allele: Dmel\ab1D
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General Information
Symbol
Dmel\ab1D
Species
D. melanogaster
Name
FlyBase ID
FBal0049273
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Key Links
Nature of the Allele
Progenitor genotype
Associated Insertion(s)
Cytology
Description

0.7kb deletion removing exon 1 of ab. The P{lwB} of ab94 has reinserted in the same position but opposite orientation.

Allele components
Component
Use(s)
Inserted element
Encoded product / tool
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

macrochaeta & wing (with ab1)

Detailed Description
Statement
Reference

Heterozygotes show an increase in wing size compared to controls.

During embryogenesis the SNb axons pause at the edge of muscle 13 and form abnormal branches, instead of forming their wild type axonal extensions onto the muscle fibers. These aberrant branches wander over the prospective target muscles and occasionally form connections at ectopic sites. Mutants do not establish the three branched terminal arbor on muscles 7, 6, 13 and 12. The transverse nerve is often incomplete and invades the ventral muscle field. A few muscles (3, 5, 11, 20) show variably penetrant defects in their attachment to the epidermis, and variable defects in the location of their attachments. Severe wing venation defect when transheterozygous with ab94. Wing veins of ab1/ab1D heterozygous adults are absent between the margin and the posterior crossvein. Thoracic and wing mechanosensory bristles are missing. Occasionally one of the campaniform sense organs on wing vein L3 is absent. Legs are gnarled and the more distal segments are reduced in length or absent; male genitalia rotated.

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

The presence of ab1D/+ reduces the frequency of incomplete border migration in animals expressing EcRB1-ΔC655.F645A.Scer\UAS under the control of Scer\GAL4slbo.2.6 to 34% of stage 10 egg chambers.

The reduction in bouton number at the NMJ that is seen in let-7KO.C mir-125KO.C double mutant animals at 96 hours APF is significantly rescued by ab1D/+.

Xenogenetic Interactions
Statement
Reference
Complementation and Rescue Data
Comments
Images (0)
Mutant
Wild-type
Stocks (1)
Notes on Origin
Discoverer
Comments
Comments

Alleles fall into an allelic series with respect to wing venation and bristle defects: ab1/ab1 = ab94/ab94 < ab1/ab60M = ab1/abG9 < ab1/ab1D = ab1/abG5.

External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (1)
References (7)