FB2024_04 , released June 25, 2024
Allele: Dmel\CG17683NC109
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General Information
Symbol
Dmel\CG17683NC109
Species
D. melanogaster
Name
FlyBase ID
FBal0244782
Feature type
allele
Associated gene
Dmel\CG17683
Associated Insertion(s)
Carried in Construct
Also Known As
Df(2R)NC109
Key Links
Genomic Maps

Allele class
Mutagen
Nature of the Allele
Allele class
Mutagen
ethyl methanesulfonate
(Myster et al., 2004)
Progenitor genotype
Cytology
Description

Amino acid replacement: V?D.

(Coulthard et al., 2010)

Location of the mutation written as the number of nucleotides downstream of the predicted translation start site.

(Coulthard et al., 2010)

Nucleotide substitution: T559A.

(Coulthard et al., 2010)

Amino acid replacement: S?A.

(Coulthard et al., 2010)

Nucleotide substitution: T564G.

(Coulthard et al., 2010)
Mutations Mapped to the Genome
Curation Data
Type
Location
Additional Notes
References
point_mutation
2R:4,131,620..4,131,620 [+]
Nucleotide change:

T4131620A

Reported nucleotide change:

T559A

Amino acid change:

V152D | CG17683-PA; V148D | CG17683-PC; V105D | CG17683-PD

Reported amino acid change:

V?D

(Coulthard et al., 2010)
point_mutation
2R:4,131,625..4,131,625 [+]
Nucleotide change:

T4131625G

Reported nucleotide change:

T564G

Amino acid change:

S154A | CG17683-PA; S150A | CG17683-PC; S107A | CG17683-PD

Reported amino acid change:

S?A

(Coulthard et al., 2010)
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
      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
      Comments
      Images (0)
      Mutant
      Wild-type
      Stocks (1)
      Notes on Origin
      Discoverer
      Comments
      Comments

      Initially described as a deletion in FBrf0174713 (and known as Df(2R)NC109 / FBab0037642 in FlyBase through to FB2010_06), but now shown to be a CG17683 allele.

      (Coulthard et al., 2010)
      External Crossreferences and Linkouts ( 0 )
      Synonyms and Secondary IDs (3)
      Reported As
      Symbol Synonym
      CG17683NC109
      Df(2R)NC109
      (Coulthard et al., 2010, Myster et al., 2004, Myster and Peifer, 2003.9.11)
      NC109
      (Coulthard et al., 2010)
      Name Synonyms
      Secondary FlyBase IDs
        References (3)