Amino acid replacement: L982term.
htk71 has no effect on the Wallerian Degeneration (programmed destruction of distal severed axons) seen in wild type wing axons following axotomy.
htk71 is a suppressor of abnormal neuroanatomy | somatic clone phenotype of Hsap\TARDBPUAS.cSa, Scer\GAL4VGlut1-OK371
htk71 is a suppressor | partially of abnormal neuroanatomy | somatic clone phenotype of Hsap\TARDBPQ331K.UAS.cSa, Scer\GAL4VGlut1-OK371
htk71 is a suppressor of leg | somatic clone phenotype of Hsap\TARDBPUAS.cSa, Scer\GAL4VGlut1-OK371
htk71 is a suppressor of motor neuron | somatic clone phenotype of Hsap\TARDBPUAS.cSa, Scer\GAL4VGlut1-OK371
htk71 is a suppressor of embryonic/larval neuromuscular junction | somatic clone phenotype of Hsap\TARDBPUAS.cSa, Scer\GAL4VGlut1-OK371
htk71 is a suppressor | partially of leg | somatic clone phenotype of Hsap\TARDBPQ331K.UAS.cSa, Scer\GAL4VGlut1-OK371
htk71 is a suppressor | partially of motor neuron | somatic clone phenotype of Hsap\TARDBPQ331K.UAS.cSa, Scer\GAL4VGlut1-OK371
htk71 partially suppresses the degeneration seen in leg motor neuron clones expressing Hsap\TARDBPQ331K.Scer\UAS.cSa under the control of Scer\GAL4VGlut-OK371. This suppression is reversed in the presence of Dp(1;3)DC353.
htk71 suppresses the degeneration seen in leg motor neuron clones expressing Hsap\TARDBPScer\UAS.cSa under the control of Scer\GAL4VGlut-OK371.