FB2024_03 , released June 25, 2024
Allele: Dmel\glo162x
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General Information
Symbol
Dmel\glo162x
Species
D. melanogaster
Name
FlyBase ID
FBal0197486
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Key Links
Genomic Maps

Nature of the Allele
Progenitor genotype
Cytology
Description

Mobilisation of P{lacW}gloS011046 produces an approximately 1.1kb deletion beginning 576bp upstream and ending 512bp downstream of the translation start codon. The deletion removes the glo transcription start site and 5' flanking region, the first and second exons, and part of the second intron for all predicted splice forms.

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

A ~1.1kb deletion resulting from the imprecise excision of P{lacW}gloS011046 that removes sequences from 576bp upstream to 512bp downstream of the translation start codon.

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

Approximately 30% of eggs laid by females with glo162x germ-line clones have abnormal dorsal appendages, ranging from short, wide appendages to fused appendages that extend laterally around the anterior of the egg. Late oocytes show a higher frequency (55%) of dorsal appendage defects, suggesting that some of these oocytes never mature as eggs. In glo162x ovaries, some egg chambers fail to undergo nurse cell dumping. In nurse cells from glo162x ovaries, chromosomes fail to disperse during mid-oogenesis and maintain a polytene morphology.

Homozygotes survive until the third instar larval stage. The class IV da neurons of the mutant larvae show a significant decrease in the number of higher order dendritic branches, as reflected by a decreased number of terminal dendritic processes.

Homozygous class IV da neuron clones show a reduction in the density of terminal dendritic branches in mosaic third instar larvae.

Over 60% of eggs produced by females with glo162x mutant ovaries (somatic clones) fail to develop beyond blastoderm stages. Between 10% and 20% of these display gross morphological defects, including abnormal dorsal appendages, collapsed appearance, or shortened egg length and are frequently unfertilised.

Approximately 25% of eggs produced by females with glo162x mutant ovaries (somatic clones) develop to hatching, while a small and variable fraction (5-10%) show defects in anterior-posterior patterning, including loss of anterior structures, loss of abdominal segments, and bicaudal phenotypes.

External Data
Interactions
Show genetic interaction network for Enhancers & Suppressors
Phenotypic Class
Suppressed by
Statement
Reference
Phenotype Manifest In
Suppressed by
Statement
Reference
Additional Comments
Genetic Interactions
Statement
Reference

A single copy of otu104 completely eliminates the dorsal appendage defects of late oocytes dissected from glo162x ovaries and reduces the nurse cell chromatin defect from 88% to 56% of egg chambers.

smg1 glo162x double mutant larvae do not show a more severe phenotype in the class IV da neurons than either single mutant.

Xenogenetic Interactions
Statement
Reference
Complementation and Rescue Data
Comments
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Mutant
Wild-type
Stocks (1)
Notes on Origin
Discoverer
External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (1)
Reported As
Name Synonyms
Secondary FlyBase IDs
    References (6)