P{EP} insertion in the first intron.
Phenotypes in the Hsap\APP1-40.Scer\UAS.T:SS-nec Alzheimer's Disease model are suppressed when tauEP3203 is transheterozygous with tauMR22.
Homozygotes have no obvious morphological or behavioural defects. The organisation of microtubules in the follicle and germline cells is indistinguishable from wild type.
tauEP3203/tauEP3203 is a suppressor | partially of bang sensitive phenotype of kccDHS1
tau[+]/tauEP3203 is a suppressor | partially of bang sensitive phenotype of kccDHS1
tauEP3203/Df(3R)MR22 is a suppressor | partially of bang sensitive phenotype of eas2
tauMR22/tauEP3203 is a suppressor of abnormal locomotor behavior | adult stage | progressive | RU486 conditional phenotype of Hsap\APPArctic.UAS.Tag:SS(nec), Scer\GAL4elav.Switch.PO
tauMR22/tauEP3203 suppresses the climbing defects seen in flies expressing Hsap\APPArctic.Scer\UAS.T:SS-nec under the control of Scer\GAL4elav.Switch.PO from 2 day post-eclosion onwards (expression induced by feeding flies RU486). This rescue is further enhanced by feeding the flies lithium in adulthood.