FB2026_03 , released September 17, 2026
Allele: Dmel\AglW1195X
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General Information
Symbol
Dmel\AglW1195X
Species
D. melanogaster
Name
FlyBase ID
FBal0351691
Feature type
allele
Associated gene
Dmel\Agl
Associated Insertion(s)
Carried in Construct
Key Links
Genomic Maps

Allele class
Mutagen
Nature of the Allele
Allele class
Mutagen
CRISPR/Cas9
(Mast and DiPrimio, 2019.7.23)
gene targeting by homologous recombination
(Mast and DiPrimio, 2019.7.23)
Progenitor genotype
Cytology
Description

A W1195term amino acid change has been introduced into the endogenous CG9485 locus. This change is equivalent to a W1099term change in the orthologous human AGL gene, a variant that is associated with Glycogen storage disease type III.

(Mast and DiPrimio, 2019.7.23)
Mutations Mapped to the Genome
Curation Data
Type
Location
Additional Notes
References
point_mutation
2R:21,318,096..21,318,096 [+]
Nucleotide change:

G21318096A

Amino acid change:

W1108term | Agl-PA; W1195term | Agl-PB; W1112term | Agl-PC; W1129term | Agl-PD; W1108term | Agl-PE; W1108term | Agl-PF

Reported amino acid change:

W1195term

Comment:

A W1195term amino acid change has been introduced into the endogenous CG9485 locus. This change is equivalent to a W1099term change in the orthologous human AGL gene, a variant that is associated with Glycogen storage disease type III. G to A nucleotide change at the second or third position of the Trp codon leads to a nonsense mutation (exact site of mutation unspecified). Site of nucleotide substitution in mutant inferred by FlyBase curator based on reported amino acid change.

(Mast and DiPrimio, 2019.7.23)
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)
       
      This allele represents a human variant implicated in disease.
      (Mast and DiPrimio, 2019.7.23)
      AGL:p.Trp1099Ter
      (FlyBase curators, 2019-)
      Variants Synonym(s)
      AGL:p.Trp1083Ter
      Associated human disease model(s)
      External database links
      ClinVar: AGL_188819
      Comments concerning this variant
      Phenotypic Data
      Phenotypic Class
      Phenotype Manifest In
      Detailed Description
      Statement
      Reference
      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
      Comments
      Images (0)
      Mutant
      Wild-type
      Stocks (1)
      Notes on Origin
      Discoverer
      External Crossreferences and Linkouts ( 0 )
      Synonyms and Secondary IDs (2)
      Reported As
      Symbol Synonym
      AglW1195X
      CG9485W1195X
      (Mast and DiPrimio, 2019.7.23)
      Name Synonyms
      Secondary FlyBase IDs
        References (2)