FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Allele: Dmel\Ddc2b
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General Information
Symbol
Dmel\Ddc2b
Species
D. melanogaster
Name
FlyBase ID
FBal0184186
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
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Description

Contains an insertion of an extra base T at nt 269, an insertion of an extra A at 1290, an insertion of an extra base C at nt 2457, a 6bp insertion of TTTTTC at nt 2650, a 14bp insertion of ATAGAGAAATTATC at nt 2622 and a 4bp insertion of AGTA at nt 2663. Contains a deletion of the sequence ATATTTTTAAAT at base 484, a deletion of a base (A) at nt 526, a deletion of a base (C) at nt 1617, and a deletion of a base (C) at nt 1934. Nucleotide positions correspond to GenBank accession X04426. Substitutions are relative to DdcR6, GenBank accession AY197756.

Nucleotide substitution: G236C.

Nucleotide substitution: G249A.

Nucleotide substitution: G323A.

Nucleotide substitution: G358A.

Nucleotide substitution: C420T.

Nucleotide substitution: T507A.

Nucleotide substitution: A517T.

Nucleotide substitution: G543A.

Nucleotide substitution: T639A.

Nucleotide substitution: G731A.

Nucleotide substitution: G916A.

Nucleotide substitution: T928C.

Nucleotide substitution: A1462T.

Nucleotide substitution: G1524A.

Nucleotide substitution: C1685A.

Nucleotide substitution: G1690A.

Nucleotide substitution: T1932C.

Nucleotide substitution: T1957C.

Nucleotide substitution: C1981T.

Nucleotide substitution: A2014G.

Nucleotide substitution: A2116G.

Nucleotide substitution: C2161A.

Nucleotide substitution: C2365T.

Nucleotide substitution: G2435C.

Nucleotide substitution: T2444A.

Nucleotide substitution: A2452C.

Nucleotide substitution: G2453C.

Nucleotide substitution: T2454C.

Nucleotide substitution: T2455A.

Nucleotide substitution: A2594G.

Nucleotide substitution: T2598C.

Nucleotide substitution: G2610A.

Nucleotide substitution: A2614T.

Nucleotide substitution: C2640T.

Nucleotide substitution: T2642A.

Nucleotide substitution: A2648T.

Nucleotide substitution: C2665T.

Nucleotide substitution: C2851T.

Nucleotide substitution: A2860T.

Nucleotide substitution: T2945C.

Nucleotide substitution: T3068A.

Nucleotide substitution: G3371C.

Nucleotide substitution: A3554G.

Nucleotide substitution: T4214C.

Nucleotide substitution: T4221G.

Nucleotide substitution: C4497A.

Nucleotide substitution: A4498T.

Nucleotide substitution: T4654G.

Nucleotide substitution: G4694A.

Nucleotide substitution: A4939C.

Mutations Mapped to the Genome
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Synonyms and Secondary IDs (2)
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    References (1)