The Jackson Laboratory

MAPT (TAU) Models

MODELJAX #TYPEDESCRIPTIONSOURCENOMENCLATURE
MAPT(H1.0)-GR35398Gene replacement190kB human construct of H1 haplotype replacing mouse MaptKoobB6J.B6N-Tc(HSA17)2Mdk/J
MAPT(H2.1)-GR33668Gene replacement190kB human construct of H2 haplotype replacing mouse MaptKoobB6J.B6N(CBA)-Tc(HSA17)1Mdk/J
MAPT(H1.0*)P301L-GR37420Gene replacement190kB human construct of H1 haplotype with P301L variant replacing mouse MaptKoobB6J.B6N-Tc(HSA17*P301L)1Mdk/J
MAPT(H1.0*N279K)-GR35794Gene replacement190kB human construct of H1 haplotype with N279K risk variant replacing mouse MaptKoobB6J.B6N(Cg)-Tc(HSA17*N279K)1Mdk/J
MAPT 10IVS+16 C>T36664Gene replacement190kB human construct of H1 haplotype with non-coding C to T (rs63751011) mutation in intron 10 replacing mouse MaptKoobB6(Cg)-Tc(HSA17*)1Mdk/J
MAPT(H1.0*)S320F-GR40796Gene replacement190kB human construct of H1 haplotype with S320F variant replacing mouse MaptMODEL-ADB6J.Cg-Isr(HAS17;MAPT*S320F)1Adiuj/AdiujJ
MAPT(H1.0*)R406W-GR-GR40815Gene replacement190kB human construct of H1 haplotype with R406W variant replacing mouse MaptMODEL-ADB6J.Cg-Isr(HAS17;MAPT*R406W)2Adiuj/AdiujJ
MAPT 10IVS+16 C>T 36664Gene replacement190kB human construct of H1 haplotype with non-coding C to T (rs63751011) mutation in intron 10 replacing mouse MaptKoobB6(Cg)-Isr(HSA17;rs63751011-T)3Mdk/J

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