FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Allele: Dmel\spinEP822
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General Information
Symbol
Dmel\spinEP822
Species
D. melanogaster
Name
FlyBase ID
FBal0129040
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Also Known As
EP822
Key Links
Genomic Maps

Allele class
Nature of the Allele
Allele class
Progenitor genotype
Associated Insertion(s)
Cytology
Description

P{EP} insertion with the spin transcription unit.

Insertion in the middle of exon 1.

Allele components
Component
Use(s)
Mutations Mapped to the Genome
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

65% of spinEP822/spink09905 stage 14 egg chambers show persisting nurse cell nuclei, compared to 7% in controls. 24% of egg chambers display a dumpless phenotype where nurse cell cytoplasm has not been transferred to the oocyte.

65% of spinEP822/spin10403 stage 14 egg chambers show persisting nurse cell nuclei, compared to 7% in controls. 52% of egg chambers display a dumpless phenotype where nurse cell cytoplasm has not been transferred to the oocyte.

73% of spinEP822 germ line clone stage 14 egg chambers show persisting nurse cell nuclei. 27% of egg chambers display a dumpless phenotype where nurse cell cytoplasm has not been transferred to the oocyte.

Mutation is lethal at the pharate pupal stage. Heterozygotes, homozygotes and spinEP822/Df(2R)Jp4 hemizygotes show a significant increase in bouton number at the larval neuromuscular junction (assayed at muscles 6/7 in hemisegment A3) compared to wild type.

The abdominal part of the CNS is abnormally long in homozygous adults compared to heterozygous or wild-type adults. This long-abdominal-ganglion phenotype becomes evident between 24 and 48 hours after puparium formation (APF). At 48 hours APF the abdominal ganglia are distorted in shape and the shortening of the tail part (which has occurred in wild-type animals) is incomplete. The mutant CNS does not undergo the transient peak in programmed cell death at 6 hours APF which is seen in wild-type animals.

The abdominal ganglion of mutant adult flies is longer than normal. The number of apoptotic cells in the ventral nerve cord after eclosion is the same in homozygous and control animals. In contrast, the profile of programmed cell death in the ventral nerve cord during the pupal stage is significantly different in homozygous animals compared to controls; at 6 hours after puparium formation the number of cells undergoing apoptosis in the homozygotes is significantly lower than in control animals. Dorsal appendages are well formed in stage 14 egg chambers of mutant females, but the nurse cell nuclei are still present (in contrast to controls, where the nurse cell nuclei have degenerated by this stage) and some earlier stage egg chambers are degenerated.

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
Fails to complement
Comments
Images (0)
Mutant
Wild-type
Stocks (0)
Notes on Origin
Discoverer
External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (3)
Reported As
Symbol Synonym
Name Synonyms
Secondary FlyBase IDs
    References (7)