FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Allele: Dmel\Syt1T7
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General Information
Symbol
Dmel\Syt1T7
Species
D. melanogaster
Name
FlyBase ID
FBal0032854
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Key Links
Nature of the Allele
Progenitor genotype
Cytology
Description

No obvious rearrangement as detected by Southern blot.

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
Detailed Description
Statement
Reference

Syt1AD1/Syt1T7 synapses (which lack the C[[2]]B domain) exhibit decreased evoked neurotransmitter release compared to wild-type controls.

Syt1AD3/Syt1T7 synapses have a rate constant that is not statistically different from wild-type controls.

There is a decrease in the overall number of synaptic vesicles at the photoreceptor synapses in sytAD1/sytT7 mutants.

No obvious morphological defects.

Transheterozygote combinations with other syt alleles are lethal.

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
Images (0)
Mutant
Wild-type
Stocks (0)
Notes on Origin
Discoverer
Comments
Comments

Isolated on basis of failure to complement Df(2L)DTD2. The syt alleles form a series: going from most severe to least severe, sytN19 = sytN6 >= sytT7 = sytT41 > sytT77 = syt66.4 > sytT11.

Mutant phenotype cannot be rescued when homozygous but can when in trans to sytN6 by sytelav.PD.

External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (2)
Reported As
Symbol Synonym
Name Synonyms
Secondary FlyBase IDs
    References (5)