FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Allele: Dmel\Nfa-swb
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General Information
Symbol
Dmel\Nfa-swb
Species
D. melanogaster
Name
facet-strawberry
FlyBase ID
FBal0012874
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Also Known As
faswb
Key Links
Allele class
Mutagen
Nature of the Allele
Allele class
Mutagen
Progenitor genotype
Caused by aberration
Cytology

Deficiency for interband between 3C6 and 7, causing these bands to fuse (Keppy and Welshons, 1977).

Description

Small deletion 5' of N.

800bp deletion removing the 3' part of the gene immediately upstream of N and almost all of the sequences up to the N transcription start site.

A complex event involving 2 deletions that result in a 880bp deletion at the distal end of N.

Deletion of 0.8kb DNA from the 5' end of the N locus.

0.8kb deletion between coordinates -27.3 and -26.0 (zero coordinate is defined as the centre of the 2.2kb EcoRI fragment that encompasses the N76b8 inversion breakpoint).

0.8 kb deletion in -28.4 to -27.1 Caused by a deficiency of 800 base pairs in the restriction fragment -- 26.2 to -- 25.0 (Grimwade, Muskavitch, Welshons, Yedvobnick and Artavanis-Tsakonas, 1985; this is 67 base pairs upstream from the start of transcription of Notch. Deletes the 3' end of the locus immediately to the left of N (Kidd, Kelley and Young, 1986).

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 ( 1 )
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

Differentiation of primary pigment cells varies between ommatidia.

Disrupted transverse rows of bristles on the first tarsal segments, few extra sex cob bristles and rough eyes.

Interacts with Df(1)rst2 to suppress eye roughening.

Homozygotes exhibit rough eyes.

Pronounced eye phenotype. Does not interact with dxENU.

Phenotype is similar to Nfa-g; flies have rough, glossy eyes. The eye phenotype is less mutant in homozygous females than hemizygous males. Nfa-swb/Nfa-g flies have rough eyes that are not glossy.

In males, eyes are rough with a variable tendency to be glossy; with Nfa-g and Nfa-g62, eyes are very rough, but mutant condition is not as extreme as that found in homozygous glossy-eyed mutants. In heterozygotes with Nfa-1, eyes are slightly rough, overlapping wild type; with spl, the eyes are wild type. The Nfa-swb allele, like Nfa-1, is not dosage compensated and the mutant condition is poorly expressed in females. Nfa-swb/Nnd-3 has slight deltas at junction of longitudinal veins with marginal veins; in heterozygotes of Nfa-swb, N55e11 and N264-40, the eyes are glossy and the Notch phenotype is enhanced, resulting in reduced viability and fertility; with the temperature-sensitive N60g11, heterozygotes are less mutant, viable, and fertile. In double mutants, Nfa-swb Nfa-g, the males have Nfa-g-like eyes; and wing veins are thickened and δ like at tips; they resemble Nnd-3 males except that wings are seldom notched. The wing-venation effect is less extreme in homozygous females (Welshons and Keppy, 1975; Keppy and Welshons, 1977). Removal of the region of 3C2-5 from the vicinity of Nfa-swb, either by deletion or inversion results in suppression of Nfa-swb; also affected by spontaneously arising, cis-acting enhancer e(fa<up>swb)</up> and suppressor su(fa<up>swb)</up> mutations, both of which map to the 3C2-5 region. (Welshons and Welshons, 1986).

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

Nfa-swb has eye phenotype, enhanceable by e(faswb)1

Suppressed by
Statement
Reference

Nfa-swb has phenotype, suppressible by In(1)78b

Nfa-swb has phenotype, suppressible by su(faswb)1

Other
Additional Comments
Genetic Interactions
Statement
Reference

Synergistic interactions with dx alleles.

The phenotype is enhanced by e(faswb)1; e(faswb)1 in cis with Nfa-swb in either the homozygous or hemizygous condition produces flies with darkly pigmented, very rough, slightly narrow eyes. In addition there is a proliferation of microchaetae over the thorax, abdomen and legs, and the tibiae of the rear legs are distinctly bowed. The phenotype is suppressed by su(faswb)1 in cis with Nfa-swb in either the homozygous or hemizygous condition. The phenotype is also suppressed by In(1)78b.

Xenogenetic Interactions
Statement
Reference
Complementation and Rescue Data
Rescued by
Not rescued by
Comments

N+tCos479 rescues the mutant phenotype but NmMGIIa construct only partially rescues.

Nfa-swb complements nd and Nnd-2.

Images (1)
Stocks (1)
Notes on Origin
Discoverer

Lefevre and Kelley.

External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (5)
References (20)