Subject: miniwhite in BSC deletions
The following information was provided to the Bloomington Stock Center by
Jim Mason, NIEHS (10/04).
Df(3L)BSC8 (FBab0029684)
The miniwhite marker from P{lacW}l(3)j11B2j11B2 was deleted or disrupted.
Df(3L)BSC10 (FBab0029692)
The miniwhite markers from both P{lacW}mirrcre2 and P{lacW}RpS12s2783
were deleted or disrupted.
Df(2R)BSC11 (FBab0029712)
The miniwhite marker from P{lacW}l(2)s3475s3475 was deleted or disrupted.
Df(3L)BSC13 (FBab0029723)
The miniwhite markers from both P{lacW}Nmtj1C7 and P{EP}ergic53EP3212
were deleted or disrupted.
Df(2L)BSC16 (FBab0029789)
The miniwhite marker from P{lacW}exk12193 was deleted or disrupted.
Df(2L)BSC17 (FBab0029725)
The miniwhite marker from P{EP}DrefEP460 was deleted or disrupted.
Df(2R)BSC18 (FBab0029741)
The miniwhite markers from both P{lacW}mamk02214 and P{EP}EP993 were
deleted or disrupted.
Df(2R)BSC19 (FBab0029795)
The miniwhite markers from both P{EP}EP951 and P{lacW}l(2)s4831s4831 were
deleted or disrupted.
Df(2R)BSC22 (FBab0029834)
The miniwhite marker from P{EP}betaTub56DEP2640 was deleted or disrupted.
Df(3L)BSC23 (FBab0029837)
The deficiency chromosome retains the miniwhite marker from
P{lacW}dosP115 and/or P{lacW}Hsp83j5C2.
Df(3L)BSC27 (FBab0029948)
The miniwhite marker from P{lacW}l(3)L4060L4060 was deleted or disrupted.
Df(2L)BSC28 (FBab0029867)
The deficiency chromosome retains the miniwhite marker from P{EP}EP2297.
Df(2R)BSC29 (FBab0029979)
The miniwhite marker from P{lacW}l(2)k09501k09501 was deleted or disrupted.
Df(3L)BSC33 (FBab0029990)
The deficiency chromosome retains the miniwhite marker from
P{lacW}Cdc27L7123 and/or P{lacW}l(3)j1D5j1D5.
Df(2L)BSC37 (FBab0037634)
The deficiency chromosome retains the miniwhite marker from P{EP}dppEP2232.
Df(3R)BSC38 (FBab0036258)
The deficiency chromosome retains the miniwhite marker from P{EP}EP3681
and/or P{EP}EP3340EP3340.
Df(2R)BSC39 (FBab0037639)
The miniwhite marker from P{GT1}Rep1BG01033 was deleted or disrupted.
Df(2R)BSC40 (FBab0037640) The deficiency chromosome retains the miniwhite
marker from P{GT1}Rep1BG01033.
Df(3R)BSC42 (FBab0037759)
The miniwhite marker from P{EP}EP3088 was deleted or disrupted.
Df(3R)BSC43 (FBab0037760)
The deficiency chromosome retains the miniwhite marker from
P{lacW}Rab11j2D1.
Df(2R)BSC44 (FBab0037744)
The deficiency chromosome retains the miniwhite marker from
P{lacW}l(2)k04222bk04222b and/or P{EP}CG14478EP2283.
Df(2R)BSC45 (FBab0037745)
The deficiency chromosome retains the miniwhite marker from
P{lacW}l(2)k07406k07406 and/or P{SUPor-P}CG6424KG00595.
Df(3L)BSC46 (FBab0037753)
The miniwhite marker from P{EP}EP771 was deleted or disrupted.
Df(3R)BSC47 (FBab0037761)
The miniwhite markers from both P{EP}CG31549EP3625 and
P{EP}CG2017EP3503 were deleted or disrupted.
Df(3R)BSC48 (FBab0037762)
The miniwhite marker from P{EP}EP3281 was deleted or disrupted.
Df(2R)BSC49 (FBab0037746)
The deficiency chromosome retains the miniwhite marker from P{EP}EP2344
and/or P{EP}CG14478EP2283.
Df(2L)BSC50 (FBab0037839)
The deficiency chromosome retains the miniwhite marker from
P{EP}CG13130EP2238 and/or P{EPgy2}EY03684.
Df(2L)BSC51 (FBab0037840)
The miniwhite markers from both P{GT1}CG15636BG01429 and P{GT1}BG01694
were deleted or disrupted.
Df(2L)BSC52 (FBab0037841)
The deficiency chromosome retains the miniwhite marker from
P{GT1}CG15636BG01429.