Mobilisation of P{EP}dbrEP2220 has produced a new insertion, 489bp upstream of the initiator ATG codon dbr.
dbrEP9 homozygotes and dbrEP9/Df(2L)PM44 animals survive until the larval (90%) and early pupal (10%) stages. In adult wings dbrEP9 mutant clones near the A/P border are associated with pattern malformations: a greater distance between veins 3 and 4 and formation of extra crossvein 1 or extra vein 3 in part. Clones located between vein 1 and 2, are phenotypically wild-type.
dbrEP9, Scer\GAL4GMR.PU is a suppressor of visible phenotype of Hsap\HSPA1LK71E.UAS, Scer\GAL4GMR.PU
dbrEP9, Scer\GAL4GMR.PU is a suppressor of abnormal neuroanatomy | adult stage phenotype of Hsap\ATXN3tr.Q78.UAS.Tag:HA, Scer\GAL4GMR.PU
dbrEP9, Scer\GAL4GMR.PU is a suppressor of eye phenotype of Hsap\HSPA1LK71E.UAS, Scer\GAL4GMR.PU
dbrEP9, Scer\GAL4GMR.PU is a suppressor of eye phenotype of Hsap\ATXN3tr.Q78.UAS.Tag:HA, Scer\GAL4GMR.PU
dbrEP9 is a weak suppressor of the eye degeneration phenotype caused by expression of Hsap\ATXN3tr.Q78.Scer\UAS.T:Ivir\HA1 under the control of Scer\GAL4GMR.PU.
dbrEP9 is partially rescued by Scer\GAL4hs.PB, dbrEP9
Scer\GAL4hs.PB, dbrEP9 partially rescues dbrEP9
Survival of dbrEP9 homozygotes to pupal stages is increased from 10% to 40% at 25oC by Scer\GAL4hs.PB.
Rescuable by precise excision.