FB2025_01 , released February 20, 2025
Allele: Dmel\tor12D
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General Information
Symbol
Dmel\tor12D
Species
D. melanogaster
Name
FlyBase ID
FBal0016920
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Also Known As
torY9
Key Links
Genomic Maps

Nature of the Allele
Progenitor genotype
Cytology
Description

Amino acid replacement: W317R.

Trp at residue 317 (in the extracellular domain) replaced by Arg.

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

T7707594A

Reported nucleotide change:

T?A

Amino acid change:

W317R | tor-PA; W317R | tor-PD

Reported amino acid change:

W317R

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

Embryos from homozygous tor12D mutant females show expanded terminal regions at the expense of central body regions, as indicated by the deletion of several abdominal segments.

The cuticle phenotype of tor12D is dosage sensitive; embryos derived from homozygous mothers show the strongest gain-of-function phenotype, while those from heterozygous or hemizygous females show progressively weaker phenotypes. Only a hollow shell of vitelline membrane can usually be found in cuticle preparations of embryos derived from homozygous females. There are no remnants of ventral denticle bands or the head skeleton. The Filzkorper, if present, appear diffuse and are mislocalised, usually in the centre of the embryo (class I phenotype). Embryos derived from heterozygous females also show a temperature sensitive cuticle phenotype. At 18oC, heterozygous females lay eggs with the most severe defects; most of the embryos have a remnant of a head skeleton, essentially all central structures are undifferentiated expect for an occasional strip of ventral denticle band and the Filzkorper is often a little enlarged (class II phenotype). At 21oC, most embryos derived from heterozygous females have an intact head skeleton and Filzkorper, and about four denticle bands are usually identifiable (class III phenotype). At 25oC, many embryos derived from heterozygous females hatch, forming nearly morphologically normal crawling larvae (sometimes one or two ventral denticle bands are missing) (class IV phenotype). torrv66 partially suppresses the cuticle defects seen in embryos derived from tor12D/+ females.

Embryos laid by heterozygous females lack most denticle belts and ectopic Filzkorper material is occasionally seen.

Embryos laid by heterozygous females lack all ventral denticle belts and the filzkorper are slightly enlarged.

Embryos derived from heterozygous females have a normal or enlarged head and telson, but the segmented region is disrupted and segments are variably deleted. Embryos derived from tor12D/+ ; tsl4/tsl4 females have the same phenotype as embryos derived from tor12D/+ females, indicating that tsl functions upstream of tor.

semidominant

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

tor12D has phenotype, suppressible by Df(2L)TE29Aa-11/Btkk00206

NOT suppressed by
Statement
Reference
NOT Enhancer of
Statement
Reference
NOT Suppressor of
Statement
Reference

tor12D is a non-suppressor of filzkorper | maternal effect phenotype of psqrum

Additional Comments
Genetic Interactions
Statement
Reference

All embryos from homozygous psqrum tor12D double mutant females show terminal defects resembling the psqrum single mutant phenotype.

The segmentation phenotype seen in embryos derived from tor12D/+ females is suppressed if the females also carry Stat92E06346 homozygous germline clones. These embryos have phenotypes similar to embryos derived from Stat92E homozygous germline clones.

The tor12D maternal effect phenotype is partially suppressed by homozygosity for Btk29Ak00206; embryos show a significant increase in the number of ventral denticle belts. The tor12D phenotype is also partially suppressed by Btk29Ak00206/Df(2L)TE29Aa-11.

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

Klingler.

External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (4)
References (22)