FB2024_03 , released June 25, 2024
Allele: Dmel\sdtXN
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General Information
Symbol
Dmel\sdtXN
Species
D. melanogaster
Name
FlyBase ID
FBal0218370
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Also Known As
sdtXN05, sdtN5
Key Links
Genomic Maps

Nature of the Allele
Progenitor genotype
Cytology
Description

Nucleotide substitution: G?A. The mutation is within the 3' splice junction of exon 6.

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

G8237170A

Reported nucleotide change:

G?A

Comment:

A G to A mutation in the splice donor site.

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 ( 1 )
Disease
Evidence
References
Modifiers Based on Experimental Evidence ( 1 )
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

Homozygous eye clones have photoreceptors with normally shaped rhabdomeres. The stalk membrane is reduced by approximately 50% in these mutant photoreceptors. The mutant photoreceptors undergo retinal degeneration when exposed to light. This light-induced degeneration is strongly reduced if the animals are raised and maintained on vitamin A-depleted medium.

Homozygous embryos derived from germ line clones exhibit severe malformations or an absence of epidermis. sdtXN bazYD double mutants exhibit abnormal zonula adherens formation and mislocalisation of membrane protein neurotactin, phenotype is stronger than sdtXP single mutant. Double mutants exhibit early cell shape changes, the surface of early gastrulating embryos shows irregularly shaped cell apices and in some areas may be multilayered by mid-gastrulation. Ultimately the cells undergo a complete transformation from epidermal to a mesenchymal-like morphology.

No changes in phenotype of tor13D embryos.

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

sdt[+]/sdtXN is an enhancer of eye phenotype of Hsap\MAPTUAS.cWa, Scer\GAL4GMR.PF

Other
Additional Comments
Genetic Interactions
Statement
Reference

Marked clones in the eye disc expressing Ras85DV12.Scer\UAS under the control of Scer\GAL4Act5C.PI and which are also homozygous for sdtN5 show metastatic behaviour.

Most sdtXN baz4 double mutant embryos do not secrete any cuticle, while some embryos have a small number of cuticle grains that appear solid, rather than vesicular. The amount of cuticle produced in sdtXN baz4 mutant embryos is not significantly increased if they also carry Df(3L)H99.

Xenogenetic Interactions
Statement
Reference
Complementation and Rescue Data
Images (0)
Mutant
Wild-type
Stocks (2)
Notes on Origin
Discoverer
Comments
Comments

Maternal germline clonal analysis demonstrates there is no maternal effect.

External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (6)
References (15)