FB2025_01 , released February 20, 2025
Allele: Dmel\scuD
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General Information
Symbol
Dmel\scuD
Species
D. melanogaster
Name
FlyBase ID
FBal0291331
Feature type
allele
Associated gene
Dmel\scu
Associated Insertion(s)
Carried in Construct
Key Links
Genomic Maps

Allele class

amorphic allele - molecular evidence

Mutagen
Nature of the Allele
Allele class

amorphic allele - molecular evidence

(Saoji et al., 2021)
Mutagen
ethyl methanesulfonate
(Yamamoto et al., 2013-)
Progenitor genotype
Cytology
Description

Amino acid replacement: S163F.

(Yamamoto et al., 2013-)
Mutations Mapped to the Genome
Curation Data
Type
Location
Additional Notes
References
point_mutation
X:18,092,430..18,092,430 [+]
Nucleotide change:

C18092430T

Amino acid change:

S163F | scu-PA; S34F | scu-PB

Reported amino acid change:

S163F

Comment:

Site of nucleotide substitution in mutant inferred by FlyBase based on reported amino acid change.

(Yamamoto et al., 2013-)
Variant Molecular Consequences
Associated Sequence Data
DDBJ / EMBL / GenBank
DNA sequence
Protein sequence
 
UniProtKB/Swiss-Prot
    UniProtKB/TrEMBL
      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

      scuD homozygote mutants display delay in pupariation compared to heterozygote sibling controls and although majority of the mutant animals does pupariate eventually, they all fail to eclose and survive to adulthood. High proportion of scuD mutants also show pupal case defects - incomplete or failed spiracle eversion.

      scuD homozygous mutants display mitochondrial morphology defects in larval brain neuroblasts: the mitochondria are larger and swollen and often have ring-like shape.

      (Sen et al., 2016)
      External Data
      Interactions
      Show genetic interaction network for Enhancers & Suppressors
      Phenotypic Class
      Phenotype Manifest In
      Additional Comments
      Genetic Interactions
      Statement
      Reference
      Xenogenetic Interactions
      Statement
      Reference
      Complementation and Rescue Data
      Images (0)
      Mutant
      Wild-type
      Stocks (0)
      Notes on Origin
      Discoverer
      External Crossreferences and Linkouts ( 0 )
      Synonyms and Secondary IDs (1)
      Reported As
      Symbol Synonym
      scuD
      (Saoji et al., 2021, Schulze and Bellen, 2016.11.29, Sen et al., 2016, Yamamoto et al., 2013-)
      Name Synonyms
      Secondary FlyBase IDs
        References (4)