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.
G10012127Y
E500D | Dna2-PB; E499D | Dna2-PC
E500D
Site and nature of nucleotide substitution in mutant inferred by FlyBase curator based on reported amino acid change.
G10012163Y
L512F | Dna2-PB; L511F | Dna2-PC
L512F
Site and nature of nucleotide substitution in mutant inferred by FlyBase curator based on reported amino acid change.
A10012397G
S571G | Dna2-PB; S570G | Dna2-PC
S571G
Site and nature of nucleotide substitution in mutant inferred by FlyBase curator based on reported amino acid change.
G10012400C
E572Q | Dna2-PB; E571Q | Dna2-PC
E572Q
Site and nature of nucleotide substitution in mutant inferred by FlyBase curator based on reported amino acid change.
A10012583G
I633V | Dna2-PB; I632V | Dna2-PC
I633V
Site and nature of nucleotide substitution in mutant inferred by FlyBase curator based on reported amino acid change.
T10012949A
C755S | Dna2-PB; C754S | Dna2-PC
C755S
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.
A10013160C
E825A | Dna2-PB; E824A | Dna2-PC
E825A
Site and nature of nucleotide substitution in mutant inferred by FlyBase curator based on reported amino acid change.
A10013162G
K826E | Dna2-PB; K825E | Dna2-PC
K826E
Site and nature of nucleotide substitution in mutant inferred by FlyBase curator based on reported amino acid change.
T10013298A
L871term | Dna2-PB; L870term | Dna2-PC
L871term
Site and nature of nucleotide substitution in mutant inferred by FlyBase curator based on reported amino acid change.
mitosis & nuclear chromosome
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.
Fails to complement mus109unspecified for female sterility.
Boyd.