FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Allele: Dmel\spdoC55
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General Information
Symbol
Dmel\spdoC55
Species
D. melanogaster
Name
FlyBase ID
FBal0050554
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Also Known As
sanpodoC55
Key Links
Genomic Maps

Nature of the Allele
Progenitor genotype
Cytology
Description

Amino acid replacement: L504R.

Amino acid replacement: L??.

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

T30478402G

Amino acid change:

L504R | spdo-PA

Reported amino acid change:

L504R

Comment:

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

Homozygous clones in the adult thorax result in a significant loss of bristles.

Homozygous clones in the thorax show extensive bristle loss.

Adult thoraces carrying spdoC55 mutant clones contain large bald patches due to the absence of external sensory structures.

The dorsal bipolar dendritic (dbd) and dorsal dendritic arbor (dda) neurons are duplicated in mutant embryos.

Increased numbers of svp expressing cardioblasts are seen in mutant embryos - up to seven or eight per segment.

Shows severe phenotype in trans to Df(3R)tll-g. spdoC55 mutant embryos show a loss of all glial cells per hemisegement in the peripheral nervous system except one. These embryos also have reduced numbers of central nervous system glia and gaps in longitudinal tracts of the ventral nerve cord. The anterior and posterior commissures appear thicker and less condensed than normal.

Defect in embryonic PNS development: gain of neurons, glial support cells are transformed into neurons.

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

Expression of spdoScer\UAS.T:Avic\GFP-EGFP under the control of either Scer\GAL4sca-DB or Scer\GAL4sca-109-68 rescues loss of bristle phenotype of spdoC55 clones in the adult thorax.

Expression of spdoLHAAA.Scer\UAS.T:Avic\GFP-EGFP under the control of Scer\GAL4sca-DB rescues loss of bristle phenotype of spdoC55 clones in the adult thorax.

Expression of spdoΔ100-125.Scer\UAS.T:Avic\GFP-EGFP under the control of Scer\GAL4sca-109-68 fails to rescue loss of bristle phenotype of spdoC55 clones in the adult thorax.

Expression of spdoΔNPAF.LHAAA.Scer\UAS.T:Avic\GFP-EGFP under the control of Scer\GAL4sca-DB rescues the loss of bristle phenotype of spdoC55 clones in the adult thorax. However, 29.9% of the rescued bristles have supernumerary socket cells.

Images (0)
Mutant
Wild-type
Stocks (1)
Notes on Origin
Discoverer
External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (3)
Reported As
Name Synonyms
Secondary FlyBase IDs
    References (16)