FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Allele: Dmel\Dna2D1
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General Information
Symbol
Dmel\Dna2D1
Species
D. melanogaster
Name
FlyBase ID
FBal0012614
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Also Known As
mus109D1
Key Links
Genomic Maps

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

Amino acid replacement: E500D.

Contains eight missense mutations, all of which likely affect the functionality of the Dna2 gene product, followed by a nonsense mutation in the 'helicase 2A' domain at codon L871.

Amino acid replacement: L512F.

Amino acid replacement: S571G.

Amino acid replacement: E572Q.

Amino acid replacement: I633V.

Amino acid replacement: C755S.

Amino acid replacement: E825A.

Amino acid replacement: K826E.

Amino acid replacement: L871term.

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

G10012127Y

Amino acid change:

E500D | Dna2-PB; E499D | Dna2-PC

Reported amino acid change:

E500D

Comment:

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

Nucleotide change:

G10012163Y

Amino acid change:

L512F | Dna2-PB; L511F | Dna2-PC

Reported amino acid change:

L512F

Comment:

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

Nucleotide change:

A10012397G

Amino acid change:

S571G | Dna2-PB; S570G | Dna2-PC

Reported amino acid change:

S571G

Comment:

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

Nucleotide change:

G10012400C

Amino acid change:

E572Q | Dna2-PB; E571Q | Dna2-PC

Reported amino acid change:

E572Q

Comment:

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

Nucleotide change:

A10012583G

Amino acid change:

I633V | Dna2-PB; I632V | Dna2-PC

Reported amino acid change:

I633V

Comment:

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

Nucleotide change:

T10012949A

Amino acid change:

C755S | Dna2-PB; C754S | Dna2-PC

Reported amino acid change:

C755S

Comment:

A nucleotide change at the first (T to A) or second (G to C) position of the Cys codon leads to a Ser mutation (base change unspecified). Site and nature of nucleotide substitution in mutant inferred by FlyBase curator based on reported amino acid change.

Nucleotide change:

A10013160C

Amino acid change:

E825A | Dna2-PB; E824A | Dna2-PC

Reported amino acid change:

E825A

Comment:

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

Nucleotide change:

A10013162G

Amino acid change:

K826E | Dna2-PB; K825E | Dna2-PC

Reported amino acid change:

K826E

Comment:

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

Nucleotide change:

T10013298A

Amino acid change:

L871term | Dna2-PB; L870term | Dna2-PC

Reported amino acid change:

L871term

Comment:

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

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

mitosis & nuclear chromosome

Detailed Description
Statement
Reference

Dna2D1/Dna2D1, Dna2D1/Dna2D2 and Dna2D1/Dna2lS individuals show increased sensitivity to the mutagen MMS.

mus109D1 mutants have a similar frequency of single-strand annealing repair (SSA) compared to controls in a P{wIw.FRT} hemizygous assay to study DNA double-stranded break repair when assayed at 32oC or 38oC.

Homozygotes and hemizygotes show a higher frequency of spontaneous chromosome aberrations in neuroblast metaphases than wild-type larvae. The ratio of chromatid breaks to isochromatid breaks is 0.7-0.8. Approximately 80% of the breaks are heterochromatic. The breaks appear to be randomly distributed among the chromosomes. The frequency of breaks is the same in females and males.

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
Fails to complement
Comments

Fails to complement mus109unspecified for female sterility.

Images (0)
Mutant
Wild-type
Stocks (0)
Notes on Origin
Discoverer

Boyd.

External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (5)
Reported As
Symbol Synonym
Dna2D1
mus-109D1
mus107D1
Name Synonyms
Secondary FlyBase IDs
    References (6)