FB2024_03 , released June 25, 2024
Allele: Dmel\Hsp8313F3
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General Information
Symbol
Dmel\Hsp8313F3
Species
D. melanogaster
Name
FlyBase ID
FBal0049163
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Also Known As
13F3
Key Links
Genomic Maps

Nature of the Allele
Progenitor genotype
Cytology
Description

Point mutation. Amino acid replacement: R48C. Nucleotide substitution: C142T.

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

C3194640T

Reported nucleotide change:

C142T

Amino acid change:

R48C | Hsp83-PA; R48C | Hsp83-PB

Reported amino acid change:

R48C

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

Hsp8313F3/Hsp83P582 transheterozygous neuroblasts exhibit loss of apical cortical polarity at prophase.

Hsp8313F3 has no effect on an invariant bristle trait (thoracic and scutellar bristles were analysed). Hsp8313F3 has no significant effect on the trait mean of a variable bristle trait (the sternopleural, orbital, ocellar and vibrissa and carina bristles were analysed) compared to the background strain in which the Hsp8313F3 mutation was induced.

Viable in transheterozygous combination with either Hsp83e1D or Hsp83e3A; males are sterile and females are weakly fertile. Viable in transheterozygous combination with Hsp83e6A; males and females are sterile. Hsp83e1D/Hsp8313F3 and Hsp8313F3/Hsp83e3A males show defects during spermatogenesis. The number and shape of spermatocytes within 16-cell cysts are mostly normal (5-10% are abnormal). Spermatids with variable number, size and shape of nuclei and nebenkern are seen. Needle-shaped crystals are present throughout developing spermatocytes and spermatids. Individualised sperm are present but they are not motile and are fragile.

Mutation interacts genetically with the sev mutations; 'sev315' and sevS11.T:Hsap\MYC.

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

Presence of Hsp8313F3 completely eliminates all additional R7 cells in phl::tor12D.hs.sev mutants.

Dominantly suppresses the rough eye phenotype of phl::tor12D.sev.

Xenogenetic Interactions
Statement
Reference
Complementation and Rescue Data
Images (0)
Mutant
Wild-type
Stocks (0)
Notes on Origin
Discoverer
Comments
Comments

Hsp8313F3 and Hsp8319F2 are independent isolates of the same point mutation.

External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (6)
Reported As
Name Synonyms
Secondary FlyBase IDs
    References (9)