A cDNA encoding the Hsap\MAPT 1N4R isoform, mutated to carry the V337M amino acid replacement (a pathogenic variant associated with FTDP-17, Frontotemporal Dementia with Parkinsonism linked to chromosome 17), has been knocked in to the endogenous tau locus (the human coding sequence replaces the endogenous Drosophila coding sequence). A Disc\RFPDsRed(T1).3xP3.cHa marker has also been inserted, downstream of the inserted Hsap\MAPT coding sequence.
Hsap\MAPTtau.1N4R-V337M, tauhTau.1N4R-V337M has abnormal circadian rhythm | recessive | progressive phenotype
Hsap\MAPTtau.1N4R-V337M, tauhTau.1N4R-V337M has abnormal locomotor behavior | recessive | adult stage | progressive phenotype
Hsap\MAPTtau.1N4R-V337M, tauhTau.1N4R-V337M has abnormal neuroanatomy | dominant | adult stage | progressive phenotype
Hsap\MAPTtau.1N4R-V337M, tauhTau.1N4R-V337M has l-LNv neuron phenotype
Hsap\MAPTtau.1N4R-V337M, tauhTau.1N4R-V337M has adult s-LNv neuron phenotype
Hsap\MAPTtau.1N4R-V337M, tauhTau.1N4R-V337M has medulla | adult stage phenotype
Hsap\MAPTtau.1N4R-V337M, tauhTau.1N4R-V337M has axon | adult stage phenotype
Hsap\MAPTtau.1N4R-V337M, tauhTau.1N4R-V337M has microtubule | adult stage phenotype
Hsap\MAPTtau.1N4R-V337M, tauhTau.1N4R-V337M has adult deutocerebrum phenotype
Hsap\MAPTtau.1N4R-V337M, tauhTau.1N4R-V337M has axon terminus | adult stage phenotype