FB2026_02 , released June 18, 2026
Allele: Dmel\Su(var)2-HP2Q2097X
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General Information
Symbol
Dmel\Su(var)2-HP2Q2097X
Species
D. melanogaster
Name
FlyBase ID
FBal0193332
Feature type
allele
Associated gene
Dmel\Su(var)2-HP2
Associated Insertion(s)
Carried in Construct
Key Links
Genomic Maps

Allele class
Mutagen
Nature of the Allele
Allele class
Mutagen
ethyl methanesulfonate
(Shaffer et al., 2006)
Progenitor genotype
Cytology
Description

Nucleotide substitution: C?T.

(Shaffer et al., 2006)

Position of amino acid replacement is with respect to accession NP_610972.

(Shaffer et al., 2006)

Amino acid replacement: Q2097term.

(Shaffer et al., 2006)
Mutations Mapped to the Genome
Curation Data
Type
Location
Additional Notes
References
point_mutation
2R:14,610,966..14,610,966 [-]
Nucleotide change:

C14610966T

Reported nucleotide change:

C?T

Amino acid change:

Q2097term | Su(var)2-HP2-PA; Q473term | Su(var)2-HP2-PB

Reported amino acid change:

Q2097term

(Shaffer et al., 2006)
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

      Metaphases from Su(var)2-HP2Q2097X/Df(2R)B11 larval brains show a number of abnormalities (frequency of cells showing each phenotype is indicated in parentheses), such as abnormal chromosome condensation (7.4%), hypercondensed chromosomes (12.0%), hyperploid/polyploid cells (8.4%), chromosome breaks (7.4%) and precocious sister-chromatid segregation (3.7%).

      (Shaffer et al., 2006)
      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 (0)
      Notes on Origin
      Discoverer
      External Crossreferences and Linkouts ( 0 )
      Synonyms and Secondary IDs (3)
      Reported As
      Symbol Synonym
      C13
      (Shaffer et al., 2006)
      Q2097X
      (Shaffer et al., 2006)
      Su(var)2-HP2Q2097X
      Name Synonyms
      Secondary FlyBase IDs
        References (1)