FB2024_03 , released June 25, 2024
Allele: Dmel\sd9
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General Information
Symbol
Dmel\sd9
Species
D. melanogaster
Name
FlyBase ID
FBal0015355
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Also Known As
sd3L
Key Links
Genomic Maps

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

Amino acid replacement: L232term.

The coordinates given for the mutant lesion refer to the sd E21 isoform. The protein encoded by the sd E7 isoform appears to be unaffected in this mutant.

Nucleotide substitution: T?A.

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

T15823439A

Reported nucleotide change:

T?A

Amino acid change:

L162term | sd-PA; L232term | sd-PB; L162term | sd-PC; L202term | sd-PD; L232term | sd-PE; L232term | sd-PF; L232term | sd-PG; L227term | sd-PH; L227term | sd-PI; L202term | sd-PJ; L232term | sd-PK; L162term | sd-PL; L227term | sd-PM; L162term | sd-PN; L202term | sd-PO; L202term | sd-PP; L417term | sd-PQ; L232term | sd-PR; L232term | sd-PS; L167term | sd-PT; L202term | sd-PU; L227term | sd-PV

Reported amino acid change:

L232term

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

Muscle structure is generally normal in sd9 embryos, although an altered distribution of nuclei is observed.

sd9 embryos exhibit a disruption in segmental nerve branch growth. The length of SNb is shorter in sd9 mutants than in controls, and the stereotyped branching pattern is disrupted.

The waves of contraction seen in newly hatched larvae are much slower than normal in sd9 hemizygotes, taking approximately 3 times as long to pass from posterior tip to anterior tip compared to wild type.

Stage 13 hemizygous embryos often have less than the normal number of cardiac cells, and many of the remaining cardiac cells have larger nuclei than normal. Somatic muscle defects are also seen, with the ventral somatic muscles (VO4-VO6) being lost or abnormal.

Homozygotes die as first instar larvae. sd9/sdETX4 flies have a scalloped wing phenotype, with the loss of most of the wing blade tissue and erosion of the wing margin.

Dorsal medial muscles in sd9 mutants display no obvious phenotype.

Larvae exhibit slow growth. Heterozygotes with viable sd alleles exhibit an extreme wing phenotype.

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

sd9; rhea1 double mutants produce a mild somatic musculature phenotype, but otherwise are indistinguishable from rhea1 mutants.

Xenogenetic Interactions
Statement
Reference
Complementation and Rescue Data
Fails to complement
Comments
Images (0)
Mutant
Wild-type
Stocks (0)
Notes on Origin
Discoverer
External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (4)
References (9)