3Lt - 61A | 89C2 - 75C | 94A - 100F2 | 92D1 - 89C4 | 61A2 - 63B8 | 72E1 - 63B11 | 72E2 - 75C | 94A - 92E1 | 100F3 - 3Rt
One of two 3L breakpoints of In(3L)P.
One of two 3L breakpoints of In(3LR)P88.
The 3L breakpoint of In(3LR)M6.
The 3R breakpoint of In(3LR)M6.
The 3R breakpoint of In(3LR)P88.
Homozygous lethal.
E.B. Lewis and F. Bacher, Sep. 1966.
TM6 was generated via X-ray induction of In(3LR)M6 (75C;94A) on a chromosome carrying three inversions: In(3LR)P88 (61A;89CD), In(3L)P (63C;72E1-2) and In(3R)C (92D1-E1;100F2-3) (FBrf0232806).
There was a female-sterile mutation near the distal end of the e4-marked In(3R)C chromosome used as the progenitor to TM6 (FBrf0000690, FBrf0000910, FBrf0001261); consequently, deficiencies removing a region within 92F cannot be maintained over TM6 or most balancers derived from it.