FB2024_03 , released June 25, 2024
Allele: Dmel\hbs459
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General Information
Symbol
Dmel\hbs459
Species
D. melanogaster
Name
FlyBase ID
FBal0130216
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Key Links
Genomic Maps

Nature of the Allele
Progenitor genotype
Cytology
Description

Amino acid replacement: K554term.

Nucleotide substitution: A?T.

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

A15038168T

Reported nucleotide change:

A?T

Amino acid change:

K553term | hbs-PA; K553term | hbs-PB; K553term | hbs-PC

Reported amino acid change:

K554term

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

hbs459/hbs66, hbs459/hbs361, hbs459/hbs1130 or hbs459/hbs2593 eyes exhibit reduced number of Rh5 expressing R8 cells.

hbs459/+ dominantly enhances the Scer\GAL4hs.2sev>hbsVDRC.cUa-induced planar cell polarity phenotype in the eye.

hbs459/Df(2R)ED2423 mutants display a reduction in the number of notal microchaetae compared with wild-type.

hbs66/hbs459 and hbs1/hbs459 adults have rough eyes.

hbs2593/hbs459 embryos exhibit a limited number of unfused myoblasts.

Stage 12 hbs459/Df(2R)X28 or hbs459/hbs2593 embryos have a reduction in the number of visceral muscle progenitors. hbs459/Df(2R)X28, or hbs459/hbs2593 embryos The overall pattern or somatic muscles is normal, though there is a partial fusion block in embryos (especially around the heart). The unfused myoblasts can still extend filopodia. Mutant embryos also show a gut phenotype consisting of an enlarged first gut chamber, which pushes the dorsal muscles and heart upwards.

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

hbs459/hbs2593 has embryonic myoblast phenotype, enhanceable by sns[+]/snsXB3

hbs459/hbs2593 has embryonic myoblast phenotype, enhanceable by sns[+]/snsD1

Suppressed by
Enhancer of
Statement
Reference
Suppressor of
Other
Additional Comments
Genetic Interactions
Statement
Reference

dock04723 hbs459 double mutant embryos have severe defects in myoblast fusion.

Psn9/Psn143 strongly enhances the thoracic bristle loss of hbs459/Df(2R)ED2423 mutants.

The patterning defects in retinas co-expressing Arf51FGD13822 and Dcr-2Scer\UAS.cDa under the control of Scer\GAL4GMR.PF is enhanced by heterozygosity for hbs459.

snsXB3, hbs2593 / snsD1, hbs459 embryos have a relatively low number of eve-expressing DA1 founder cells - fewer than in snsXB3 embryos.

The limited number of unfused myoblasts in hbs2593/hbs459 embryos increases when embryos are also heterozygous for snsXB3 or snsD1.

Pupae heterozygous for hbs459 exhibit mild but consistent suppression of the Scer\GAL4GMR.PF>cindrdsRNA.PC.PD.Scer\UAS phenotype. The prevalence of cone and 1[o] cell defects is decreased and the number of 2[o] and 3[o] cells is reduced to slightly below normal.

Both the gut and the somatic mesoderm phenotypers seen in hbs459/hbs2593 embryos are suppressed by the addition of snsXB3.

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 (2)
References (11)