FB2024_03 , released June 25, 2024
Allele: Dmel\Trim946
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General Information
Symbol
Dmel\Trim946
Species
D. melanogaster
Name
FlyBase ID
FBal0258025
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Key Links
Allele class
Nature of the Allele
Allele class
Progenitor genotype
Cytology
Description

Imprecise excision of P{GawB}Trim9NP4638 (located 152bp upstream of the start codon of Trim9) generates a deletion within the 5'UTR and further upstream of Trim9.

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

Trim946 mutants display a droopy wing phenotype.

Trim946 mutants display aberrant class IV da neuron morphology. Axons frequently fail to cross the midline and some longitudinal tracts become thicker.

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

Trim946 has abnormal neuroanatomy phenotype, enhanceable by fra3/Df(1)NP5/fra[+]/+

Suppressed by
Statement
Reference
Phenotype Manifest In
Enhanced by
Statement
Reference

Trim946 has dopaminergic neuron phenotype, enhanceable by fra3/Df(1)NP5/fra[+]/+

Trim946 has commissure phenotype, enhanceable by robo[+]/fra3/robo11/fra[+]

Suppressed by
Statement
Reference

Trim946 has dopaminergic neuron phenotype, suppressible by robo[+]/Df(2R)BSC482/robo11/+

+:, Trim946 has commissure phenotype, suppressible by Df(2R)BSC482/Df(1)NP5/+/+

Additional Comments
Genetic Interactions
Statement
Reference

The Trim946 axon midline crossing phenotype is significantly enhanced in a Df(1)NP5 and fra3 heterozygous background.

Removal of one copy of robo1 and sli (using the deficiency Df(2R)BSC482) suppresses the axon midline crossing defect found in Trim946 mutants.

Overexpression of fraScer\UAS.cKa under the control of Scer\GAL4ppk.1.9 significantly suppresses the Trim946 midline crossing defects.

Xenogenetic Interactions
Statement
Reference
Complementation and Rescue Data
Comments

Expression of Trim9Scer\UAS.cSa in class IV da neurons under the control of Scer\GAL4ppk.1.9 fully rescues the guidance defects found in Trim946 mutants.

Images (0)
Mutant
Wild-type
Stocks (0)
Notes on Origin
Discoverer
External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (2)
Reported As
Symbol Synonym
Trim946
Name Synonyms
Secondary FlyBase IDs
    References (1)