FB2025_01 , released February 20, 2025
Allele: Dmel\Su(Tpl)S-192
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General Information
Symbol
Dmel\Su(Tpl)S-192
Species
D. melanogaster
Name
FlyBase ID
FBal0048982
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Also Known As
SR3-4AS-192
Key Links
Genomic Maps

Allele class
Nature of the Allele
Allele class
Progenitor genotype
Cytology
Description

Amino acid replacement: R916G. Amino acid replacement: D918N. Amino acid replacement: S660L.

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

C19892725T

Amino acid change:

S660L | Su(Tpl)-PA; S660L | Su(Tpl)-PB; S660L | Su(Tpl)-PC

Reported amino acid change:

S660L

Comment:

One of three @Su(Tpl) missense mutations in strain. Site of nucleotide substitution in mutant inferred by FlyBase based on reported amino acid change.

Nucleotide change:

C19891958G

Amino acid change:

R916G | Su(Tpl)-PA; R916G | Su(Tpl)-PB; R916G | Su(Tpl)-PC

Reported amino acid change:

R916G

Comment:

One of three @Su(Tpl) missense mutations in strain. Site of nucleotide substitution in mutant inferred by FlyBase based on reported amino acid change.

Nucleotide change:

G19891952A

Amino acid change:

D918N | Su(Tpl)-PA; D918N | Su(Tpl)-PB; D918N | Su(Tpl)-PC

Reported amino acid change:

D918N

Comment:

One of three @Su(Tpl) missense mutations in strain. Site of nucleotide substitution in mutant inferred by FlyBase based on reported amino acid change.

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

The hetero-allelic combination Su(Tpl)s1/Su(Tpl)S-192 is embryonic lethal. Mutant cuticles display the following defects, with variable penetrance: abdominal segment 2 missing, incomplete or fused to abdominal segment 1; abdominal segment 6 broken or fused to abdominal segment 5; abdominal segment 8 missing. The hetero-allelic combination Su(Tpl)10/Su(Tpl)S-192 is embryonic lethal. Mutant cuticles display the following defects, with variable penetrance: Mutant cuticles display the following defects, with variable penetrance: abdominal segment 2 missing, incomplete or fused to abdominal segment 3; abdominal segment 4 incomplete or fused to abdominal segment 3 or 5; metathoracic segment missing, incomplete or fused to abdominal segment 1; incomplete head involution. The hetero-allelic combination Su(Tpl)17/Su(Tpl)S-192 is embryonic lethal. Mutant cuticles display the following defects, with variable penetrance: abdominal segment 4 missing or fused to abdominal segment 3 or 5; abdominal segment 6 incomplete or fused to abdominal segment 5; incomplete head involution. The hetero-allelic combination Su(Tpl)XS-706/Su(Tpl)S-192 is embryonic lethal. Mutant cuticles display the following defects, with variable penetrance: metathoracic segment missing or fused to mesothoracic segment; abdominal segments 1, 2 and 4 often incomplete.

External Data
Interactions
Show genetic interaction network for Enhancers & Suppressors
Phenotypic Class
Enhancer of
Statement
Reference

Su(Tpl)[+]/Su(Tpl)S-192 is an enhancer of visible | dominant phenotype of Bx1

Suppressor of
Statement
Reference
Other
Phenotype Manifest In
Enhancer of
Statement
Reference

Su(Tpl)[+]/Su(Tpl)S-192 is an enhancer of wing margin phenotype of Bx1

Su(Tpl)[+]/Su(Tpl)S-192 is an enhancer of wing margin phenotype of Nnd-1

Su(Tpl)[+]/Su(Tpl)S-192 is an enhancer of wing margin phenotype of ct53d

Suppressor of
Statement
Reference

Su(Tpl)S-192 is a suppressor of phenotype of Ras85DV12.sev

Additional Comments
Genetic Interactions
Statement
Reference

The lethality caused by sevS11.T:Hsap\MYC in combination with Ras85DV12.sev is suppressed by Su(Tpl)S-192.

Suppresses the rough eye phenotype of Ras85DV12.sev. Enhances the phenotype of Ras85DN17.sev. Has little or no effect on the phenotype of phl::tor13D.hs.sev. Suppresses the phenotype of Ras85D::Src64BV12.ΔCAAX.sev. Has little or no effect on the lethality of phl12. Has little or no effect on the phl12 eye phenotype. Has little or no effect on the Dsor1XS520 eye phenotype. Enhances the aopS2382 eye phenotype.

Xenogenetic Interactions
Statement
Reference
Complementation and Rescue Data
Images (0)
Mutant
Wild-type
Stocks (1)
Notes on Origin
Discoverer
External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (6)
Reported As
Name Synonyms
Secondary FlyBase IDs
    References (9)