Associated with: spdo^H7.

Associated with: spdo^H7

Evidence suggests that the "H7" chromosome contains lesions that affect both tmod and spdo (as suggested in FBrf0182569 and FBrf0183486); the P{lacW}tmod^H7 insertion maps within the tmod transcription unit (see FBrf0102830) and the "H7" chromosome also fails to complement spdo mutations, suggesting that there is a second lesion that affects spdo. The nature of the lesion(s) is not known, however data from FBrf0183486 suggests that there may be a deletion extending from the site of the progenitor insertion to the P{lacW}tmod^H7 insertion in tmod.