The cytology reported is tentative. The rearrangement also contains In(3R)89C3-89C7;96A (possibly In(3R)P), which was presumably segregating in the progenitor stock.
T(2;3)37D3-37D7;87D + T(2;3)22A;35E-35F;49A-49B;64D-64F;66A-66B;81P;het. The cytology reported is tentative. The breakpoint in section 81 is very proximal. The proximal broken end is not distinguishable from heterochromatin. The rearrangement also contains In(3R)89C3-89C7;96A (possibly In(3R)P), which was presumably segregating in the progenitor stock.
T(2;3)37D3-37D7;87D + Tp(2;3)22A;35E-35F;49A-49B;64D-64F;66A-66B;81P;het. The cytology reported is tentative. The breakpoint in section 81 is very proximal. The proximal broken end is not distinguishable from heterochromatin. The rearrangement also contains In(3R)89C3-89C7;96A (possibly In(3R)P), which was presumably segregating in the progenitor stock.
Limits of break 1 from polytene analysis (FBrf0050013) Limits of break 2 from polytene analysis (FBrf0050013) Limits of break 3 from polytene analysis (FBrf0050013) Limits of break 4 from polytene analysis (FBrf0050013) Limits of break 5 from polytene analysis (FBrf0050013) Limits of break 6 from polytene analysis (FBrf0050013) Limits of break 7 from polytene analysis (FBrf0053709) Limits of break 8 from polytene analysis (FBrf0050013)
If no genes are listed here, it may be because the affected region is very large.
The JBrowse insert above may show an error for the same reason,
and other FlyBase tools such as CytoSearch may also fail for large regions.
You can contact FlyBase for more help.
In these cases, there will be no "Export to Hitlist" button to the left.
The cytology reported is tentative. The rearrangement also contains In(3R)89C3-89C7;96A (possibly In(3R)P), which was presumably segregating in the progenitor stock.
T(2;3)37D3-37D7;87D + T(2;3)22A;35E-35F;49A-49B;64D-64F;66A-66B;81P;het. The cytology reported is tentative. The breakpoint in section 81 is very proximal. The proximal broken end is not distinguishable from heterochromatin. The rearrangement also contains In(3R)89C3-89C7;96A (possibly In(3R)P), which was presumably segregating in the progenitor stock.
T(2;3)37D3-37D7;87D + Tp(2;3)22A;35E-35F;49A-49B;64D-64F;66A-66B;81P;het. The cytology reported is tentative. The breakpoint in section 81 is very proximal. The proximal broken end is not distinguishable from heterochromatin. The rearrangement also contains In(3R)89C3-89C7;96A (possibly In(3R)P), which was presumably segregating in the progenitor stock.
Limits of break 1 from polytene analysis (FBrf0050013) Limits of break 2 from polytene analysis (FBrf0050013) Limits of break 3 from polytene analysis (FBrf0050013) Limits of break 4 from polytene analysis (FBrf0050013) Limits of break 5 from polytene analysis (FBrf0050013) Limits of break 6 from polytene analysis (FBrf0050013) Limits of break 7 from polytene analysis (FBrf0053709) Limits of break 8 from polytene analysis (FBrf0050013)