Neuroblast NB1-1 found in an abdominal segment. It generates subperineurial glia as well as neurons (Schmid et al., 1999; Beckervordersandforth et al., 2008). It is a type II neuroglioblast and its glial progeny are part of its Notch ON hemilineage (Udolph et al., 2001). It does not produce a secondary lineage (Lacin and Truman, 2016).
Adult ascending neuron of the AN16B078 group with ipsilateral VNC arbors (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 16B hemilineage (Takemura et al., 2024; Marin et al., 2024). It exits the VNC via the cervical connective (Takemura et al., 2024; Marin et al., 2024). Within the VNC it fasciculates with the intermediate tract of dorsal cervical fasciculus - commissure of fine fibers (Takemura et al., 2024; Marin et al., 2024). It receives input in the neck neuropil and sends output to the neck neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There are approximately 13 of these cells per organism and their somas are found in the prothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult ascending neuron of the AN16B081 group with ipsilateral VNC arbors (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 16B hemilineage (Takemura et al., 2024; Marin et al., 2024). It exits the VNC via the cervical connective (Takemura et al., 2024; Marin et al., 2024). Within the VNC it fasciculates with the intermediate tract of dorsal cervical fasciculus - commissure of fine fibers (Takemura et al., 2024; Marin et al., 2024). It receives input in the neck neuropil and sends output to the neck neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There are approximately 2 of these cells per organism and their somas are found in the prothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult ascending neuron of the AN16B112 group with ipsilateral VNC arbors (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 16B hemilineage (Takemura et al., 2024; Marin et al., 2024). It exits the VNC via the cervical connective (Takemura et al., 2024; Marin et al., 2024). Within the VNC it fasciculates with the intermediate tract of dorsal cervical fasciculus - commissure of fine fibers (Takemura et al., 2024; Marin et al., 2024). It receives input in the neck neuropil and sends output to the neck neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There are approximately 4 of these cells per organism and their somas are found in the prothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult ascending neuron of the AN16B116 group with ipsilateral VNC arbors (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 16B hemilineage (Takemura et al., 2024; Marin et al., 2024). It exits the VNC via the cervical connective (Takemura et al., 2024; Marin et al., 2024). Within the VNC it fasciculates with the intermediate tract of dorsal cervical fasciculus - commissure of fine fibers (Takemura et al., 2024; Marin et al., 2024). It receives input in the neck neuropil and sends output to the neck neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There are approximately 2 of these cells per organism and their somas are found in the prothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
First born ganglion mother cell of neuroblast NB1-1.
Unilateral neuron of the HUL011 group of the adult ventral nerve cord that primarily arborizes in the haltere neuropil (Ehrhardt et al., 2023). It is an interneuron that arborizes mainly within one neuromere of the VNC (Ehrhardt et al., 2023). It has mixed arborization in the ipsilateral haltere neuropil (Ehrhardt et al., 2023). It has its soma in a anterior-ventral-medial position in the metathoracic neuromere (Ehrhardt et al., 2023). It belongs to the 16A hemilineage of the T3 neuromere (Ehrhardt et al., 2023).
Unilateral neuron of the HUL012 group of the adult ventral nerve cord that primarily arborizes in the haltere neuropil (Ehrhardt et al., 2023). It is an interneuron that arborizes mainly within one neuromere of the VNC (Ehrhardt et al., 2023). It has mixed arborization in the ipsilateral haltere neuropil (Ehrhardt et al., 2023). It has its soma in a posterior-ventral-lateral position in the metathoracic neuromere (Ehrhardt et al., 2023). It belongs to the 16A hemilineage of the T3 neuromere (Ehrhardt et al., 2023). There are three of these cells per hemineuromere (Ehrhardt et al., 2023).
Adult intrinsic neuron of the IN16B014 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a primary neuron of the 16B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the T1 leg neuropil and sends output to the T1 leg neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There are approximately 2 of these cells per organism and their somas are found in the prothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN16B016 group (Takemura et al., 2024; Marin et al., 2024). It is a primary neuron of the 16B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the leg neuropil and sends output to the leg neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There are approximately 6 of these cells per organism and their somas are found in the mesothoracic neuromere, metathoracic neuromere and prothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN16B018 group with ipsilateral arbors in a single VNC neuromere (Takemura et al., 2024; Marin et al., 2024). It is a primary neuron of the 16B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the leg neuropil and sends output to the leg neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is gaba (Eckstein et al., 2024). There are approximately 6 of these cells per organism and their somas are found in the mesothoracic neuromere, metathoracic neuromere and prothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN16B020 group (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 16B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the leg neuropil and sends output to the leg neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There are approximately 6 of these cells per organism and their somas are found in the mesothoracic neuromere, metathoracic neuromere and prothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN16B022 group with ipsilateral arbors in a single VNC neuromere (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 16B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the leg neuropil and sends output to the leg neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There are approximately 4 of these cells per organism and their somas are found in the mesothoracic neuromere and prothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN16B024 group with ipsilateral arbors in a single VNC neuromere (Takemura et al., 2024; Marin et al., 2024). It is a primary neuron of the 16B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the T3 leg neuropil and sends output to the T3 leg neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There are approximately 2 of these cells per organism and their somas are found in the metathoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN16B029 group with ipsilateral arbors in a single VNC neuromere (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 16B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the leg neuropil and sends output to the leg neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There are approximately 6 of these cells per organism and their somas are found in the mesothoracic neuromere, metathoracic neuromere and prothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN16B030 group with ipsilateral arbors in a single VNC neuromere (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 16B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the leg neuropil and sends output to the leg neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There are approximately 6 of these cells per organism and their somas are found in the mesothoracic neuromere, metathoracic neuromere and prothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN16B032 group with ipsilateral arbors in a single VNC neuromere (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 16B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the leg neuropil and sends output to the leg neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There are approximately 6 of these cells per organism and their somas are found in the mesothoracic neuromere, metathoracic neuromere and prothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN16B033 group with ipsilateral arbors in a single VNC neuromere (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 16B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the leg neuropil and sends output to the leg neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There are approximately 6 of these cells per organism and their somas are found in the mesothoracic neuromere, metathoracic neuromere and prothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN16B034 group with bilateral arbors in a single VNC neuromere (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 16B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the T1 leg neuropil and sends output to the T1 leg neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There are approximately 2 of these cells per organism and their somas are found in the prothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN16B036 group with ipsilateral arbors in a single VNC neuromere (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 16B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the leg neuropil and sends output to the leg neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There are approximately 6 of these cells per organism and their somas are found in the mesothoracic neuromere, metathoracic neuromere and prothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN16B037 group with ipsilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a primary neuron of the 16B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the leg neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There are approximately 6 of these cells per organism and their somas are found in the mesothoracic neuromere, metathoracic neuromere and prothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN16B038 group with ipsilateral arbors in a single VNC neuromere (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 16B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the T1 leg neuropil and sends output to the T1 leg neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There are approximately 2 of these cells per organism and their somas are found in the prothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN16B039 group with ipsilateral arbors in a single VNC neuromere (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 16B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the leg neuropil and sends output to the leg neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There are approximately 4 of these cells per organism and their somas are found in the mesothoracic neuromere and metathoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN16B040 group with ipsilateral arbors in a single VNC neuromere (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 16B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the T3 leg neuropil and sends output to the T3 leg neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There are approximately 2 of these cells per organism and their somas are found in the metathoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN16B041 group with ipsilateral arbors in a single VNC neuromere (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 16B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the leg neuropil and sends output to the leg neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There are approximately 6 of these cells per organism and their somas are found in the mesothoracic neuromere, metathoracic neuromere and prothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN16B042 group with ipsilateral arbors in a single VNC neuromere (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 16B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the leg neuropil and sends output to the leg neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There are approximately 12 of these cells per organism and their somas are found in the mesothoracic neuromere, metathoracic neuromere and prothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN16B045 group with ipsilateral arbors in a single VNC neuromere (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 16B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the leg neuropil and sends output to the leg neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There are approximately 12 of these cells per organism and their somas are found in the mesothoracic neuromere, metathoracic neuromere and prothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN16B046 group with ipsilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 16B hemilineage (Takemura et al., 2024; Marin et al., 2024). It sends output to the tectulum (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There are approximately 5 of these cells per organism and their somas are found in the prothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN16B047 group with ipsilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 16B hemilineage (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There are approximately 2 of these cells per organism and their somas are found in the metathoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN16B048 group with ipsilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 16B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the haltere neuropil and wing neuropil and sends output to multiple regions (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There are approximately 2 of these cells per organism and their somas are found in the metathoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN16B049 group with bilateral arbors in a single VNC neuromere (Takemura et al., 2024; Marin et al., 2024). It is a primary neuron of the 16B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the abdominal neuromere and sends output to the abdominal neuromere (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There are approximately 4 of these cells per organism and their somas are found in the abdominal neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN16B050 group with bilateral arbors in a single VNC neuromere (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 16B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the T1 leg neuropil and sends output to the T1 leg neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There are approximately 2 of these cells per organism and their somas are found in the prothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN16B051 group with ipsilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 16B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the haltere neuropil and sends output to the haltere neuropil and intermediate tectulum (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There are approximately 4 of these cells per organism and their somas are found in the metathoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN16B052 group (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 16B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the leg neuropil and sends output to the leg neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There are approximately 8 of these cells per organism and their somas are found in the mesothoracic neuromere and metathoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN16B053 group with ipsilateral arbors in a single VNC neuromere (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 16B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the T3 leg neuropil and sends output to the T3 leg neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There are approximately 4 of these cells per organism and their somas are found in the metathoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN16B054 group with ipsilateral arbors in a single VNC neuromere (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 16B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the T3 leg neuropil and sends output to the T3 leg neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There are approximately 2 of these cells per organism and their somas are found in the metathoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN16B055 group with bilateral arbors in a single VNC neuromere (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 16B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the T1 leg neuropil and sends output to the T1 leg neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There are approximately 8 of these cells per organism and their somas are found in the prothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN16B056 group with bilateral arbors in a single VNC neuromere (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 16B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the T1 leg neuropil and sends output to the T1 leg neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There are approximately 4 of these cells per organism and their somas are found in the prothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN16B057 group with ipsilateral arbors in a single VNC neuromere (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 16B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the T1 leg neuropil and sends output to the T1 leg neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There is approximately one of these cells per organism with its soma in the prothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN16B058 group with bilateral arbors in a single VNC neuromere (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 16B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the T1 leg neuropil and sends output to the T1 leg neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There are approximately 6 of these cells per organism and their somas are found in the prothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN16B059 group with ipsilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 16B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the haltere neuropil and sends output to the haltere neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There are approximately 4 of these cells per organism and their somas are found in the metathoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN16B060 group with bilateral arbors in a single VNC neuromere (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 16B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the T1 leg neuropil and sends output to the T1 leg neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There are approximately 4 of these cells per organism and their somas are found in the prothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN16B061 group with bilateral arbors in a single VNC neuromere (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 16B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the T1 leg neuropil and sends output to the T1 leg neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There are approximately 8 of these cells per organism and their somas are found in the prothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN16B062 group (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 16B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the wing neuropil and sends output to the wing neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There are approximately 4 of these cells per organism and their somas are found in the mesothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN16B063 group with ipsilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 16B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the wing neuropil and sends output to the wing neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There are approximately 4 of these cells per organism and their somas are found in the mesothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN16B064 group with ipsilateral arbors in a single VNC neuromere (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 16B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the T1 leg neuropil and sends output to the T1 leg neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There are approximately 4 of these cells per organism and their somas are found in the prothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN16B065 group with ipsilateral arbors in a single VNC neuromere (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 16B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the T2 leg neuropil and sends output to the T2 leg neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There are approximately 2 of these cells per organism and their somas are found in the mesothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN16B066 group with ipsilateral arbors in a single VNC neuromere (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 16B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the haltere neuropil and sends output to the haltere neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There are approximately 2 of these cells per organism and their somas are found in the metathoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN16B067 group with ipsilateral arbors in a single VNC neuromere (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 16B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the T3 leg neuropil and sends output to the T3 leg neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There are approximately 2 of these cells per organism and their somas are found in the metathoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN16B068 group with ipsilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 16B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the wing neuropil and sends output to the wing neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There are approximately 6 of these cells per organism and their somas are found in the mesothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN16B069 group (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 16B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the wing neuropil and sends output to the wing neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There are approximately 4 of these cells per organism and their somas are found in the mesothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN16B070 group with bilateral arbors in a single VNC neuromere (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 16B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the T1 leg neuropil and sends output to the T1 leg neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There are approximately 6 of these cells per organism and their somas are found in the prothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN16B071 group with ipsilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 16B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in multiple regions and sends output to multiple regions (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There are approximately 4 of these cells per organism and their somas are found in the mesothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN16B072 group with ipsilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 16B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the wing neuropil and sends output to the wing neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There are approximately 2 of these cells per organism and their somas are found in the mesothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN16B073 group with ipsilateral arbors in a single VNC neuromere (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 16B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the T2 leg neuropil and sends output to the T2 leg neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There are approximately 7 of these cells per organism and their somas are found in the mesothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN16B074 group with ipsilateral arbors in a single VNC neuromere (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 16B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the leg neuropil and sends output to the leg neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There are approximately 8 of these cells per organism and their somas are found in the mesothoracic neuromere and metathoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN16B075 group with ipsilateral arbors in a single VNC neuromere (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 16B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the leg neuropil and sends output to the leg neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There are approximately 20 of these cells per organism and their somas are found in the mesothoracic neuromere and prothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN16B076 group with ipsilateral arbors in a single VNC neuromere (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 16B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the T1 leg neuropil and sends output to the T1 leg neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There are approximately 2 of these cells per organism and their somas are found in the prothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN16B077 group (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 16B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the leg neuropil and sends output to the leg neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There are approximately 11 of these cells per organism and their somas are found in the mesothoracic neuromere, metathoracic neuromere and prothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN16B079 group with ipsilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 16B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in multiple regions (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There are approximately 5 of these cells per organism and their somas are found in the mesothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN16B080 group (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 16B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the T1 leg neuropil and sends output to the T1 leg neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There are approximately 3 of these cells per organism and their somas are found in the prothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN16B082 group with ipsilateral arbors in a single VNC neuromere (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 16B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the leg neuropil and sends output to the leg neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There are approximately 6 of these cells per organism and their somas are found in the mesothoracic neuromere, metathoracic neuromere and prothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN16B083 group with ipsilateral arbors in a single VNC neuromere (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 16B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the leg neuropil and sends output to the leg neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There are approximately 7 of these cells per organism and their somas are found in the mesothoracic neuromere and prothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN16B084 group with ipsilateral arbors in a single VNC neuromere (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 16B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the haltere neuropil and sends output to the haltere neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There are approximately 2 of these cells per organism and their somas are found in the metathoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN16B085 group with ipsilateral arbors in a single VNC neuromere (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 16B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the T3 leg neuropil and sends output to the T3 leg neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There are approximately 2 of these cells per organism and their somas are found in the metathoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN16B086 group with ipsilateral arbors in a single VNC neuromere (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 16B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the T3 leg neuropil and sends output to the T3 leg neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There are approximately 6 of these cells per organism and their somas are found in the metathoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN16B087 group with ipsilateral arbors in a single VNC neuromere (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 16B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the haltere neuropil and sends output to the haltere neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There are approximately 2 of these cells per organism and their somas are found in the metathoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN16B088 group with ipsilateral arbors in a single VNC neuromere (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 16B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the T3 leg neuropil and sends output to the T3 leg neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There are approximately 2 of these cells per organism and their somas are found in the metathoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN16B089 group (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 16B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the haltere neuropil and sends output to the haltere neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There are approximately 6 of these cells per organism and their somas are found in the metathoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN16B090 group with ipsilateral arbors in a single VNC neuromere (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 16B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the T2 leg neuropil and sends output to the T2 leg neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There are approximately 4 of these cells per organism and their somas are found in the mesothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN16B091 group with ipsilateral arbors in a single VNC neuromere (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 16B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the T1 leg neuropil and sends output to the T1 leg neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There are approximately 4 of these cells per organism and their somas are found in the prothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN16B092 group with ipsilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 16B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the intermediate tectulum and wing neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There are approximately 5 of these cells per organism and their somas are found in the mesothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN16B093 group with ipsilateral arbors in a single VNC neuromere (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 16B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the haltere neuropil and sends output to the haltere neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There are approximately 4 of these cells per organism and their somas are found in the metathoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN16B094 group with ipsilateral arbors in a single VNC neuromere (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 16B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the T1 leg neuropil and sends output to the T1 leg neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There are approximately 4 of these cells per organism and their somas are found in the prothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN16B095 group with ipsilateral arbors in a single VNC neuromere (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 16B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the T2 leg neuropil and sends output to the T2 leg neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There are approximately 2 of these cells per organism and their somas are found in the mesothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN16B096 group with ipsilateral arbors in a single VNC neuromere (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 16B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the T3 leg neuropil and sends output to the T3 leg neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There are approximately 2 of these cells per organism and their somas are found in the metathoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN16B097 group with ipsilateral arbors in a single VNC neuromere (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 16B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the leg neuropil and sends output to the leg neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There are approximately 6 of these cells per organism and their somas are found in the mesothoracic neuromere, metathoracic neuromere and prothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN16B098 group with ipsilateral arbors in a single VNC neuromere (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 16B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the leg neuropil and sends output to the leg neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There are approximately 7 of these cells per organism and their somas are found in the mesothoracic neuromere, metathoracic neuromere and prothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN16B099 group (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 16B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the wing neuropil and sends output to the wing neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There are approximately 11 of these cells per organism and their somas are found in the mesothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN16B100 group (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 16B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the neck neuropil and sends output to the neck neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There are approximately 9 of these cells per organism and their somas are found in the prothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN16B101 group with ipsilateral arbors in a single VNC neuromere (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 16B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the leg neuropil and sends output to the leg neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There are approximately 4 of these cells per organism and their somas are found in the mesothoracic neuromere and metathoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN16B102 group with ipsilateral arbors in a single VNC neuromere (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 16B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the T1 leg neuropil and sends output to the T1 leg neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There are approximately 2 of these cells per organism and their somas are found in the prothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN16B103 group with ipsilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 16B hemilineage (Takemura et al., 2024; Marin et al., 2024). It sends output to multiple regions (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There are approximately 2 of these cells per organism and their somas are found in the metathoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN16B104 group with ipsilateral arbors in a single VNC neuromere (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 16B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the haltere neuropil and sends output to the haltere neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There are approximately 2 of these cells per organism and their somas are found in the metathoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN16B105 group with ipsilateral arbors in a single VNC neuromere (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 16B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the T3 leg neuropil and sends output to the T3 leg neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There are approximately 4 of these cells per organism and their somas are found in the metathoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN16B106 group (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 16B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the haltere neuropil and sends output to the haltere neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There are approximately 5 of these cells per organism and their somas are found in the metathoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN16B107 group with ipsilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 16B hemilineage (Takemura et al., 2024; Marin et al., 2024). It sends output to multiple regions (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There are approximately 3 of these cells per organism and their somas are found in the metathoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN16B108 group with ipsilateral arbors in a single VNC neuromere (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 16B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the T3 leg neuropil and sends output to the T3 leg neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There are approximately 8 of these cells per organism and their somas are found in the metathoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN16B109 group with ipsilateral arbors in a single VNC neuromere (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 16B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the T3 leg neuropil and sends output to the T3 leg neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There are approximately 2 of these cells per organism and their somas are found in the metathoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN16B110 group with ipsilateral arbors in a single VNC neuromere (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 16B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the T3 leg neuropil and sends output to the T3 leg neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There are approximately 2 of these cells per organism and their somas are found in the metathoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN16B111 group with ipsilateral arbors in a single VNC neuromere (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 16B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the haltere neuropil and sends output to the haltere neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There are approximately 4 of these cells per organism and their somas are found in the metathoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN16B113 group with ipsilateral arbors in a single VNC neuromere (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 16B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the T2 leg neuropil and sends output to the T2 leg neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There are approximately 2 of these cells per organism and their somas are found in the mesothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN16B114 group with ipsilateral arbors in a single VNC neuromere (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 16B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the T1 leg neuropil and sends output to the T1 leg neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There are approximately 5 of these cells per organism and their somas are found in the prothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN16B115 group with ipsilateral arbors in a single VNC neuromere (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 16B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the T1 leg neuropil and sends output to the T1 leg neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There are approximately 2 of these cells per organism and their somas are found in the prothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN16B117 group with ipsilateral arbors in a single VNC neuromere (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 16B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the T2 leg neuropil and sends output to the T2 leg neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There are approximately 2 of these cells per organism and their somas are found in the mesothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN16B118 group with ipsilateral arbors in a single VNC neuromere (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 16B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the T3 leg neuropil and sends output to the T3 leg neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There are approximately 4 of these cells per organism and their somas are found in the metathoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN16B119 group with ipsilateral arbors in a single VNC neuromere (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 16B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the T3 leg neuropil and sends output to the T3 leg neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There are approximately 3 of these cells per organism and their somas are found in the metathoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN16B120 group with ipsilateral arbors in a single VNC neuromere (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 16B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the T3 leg neuropil and sends output to the T3 leg neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There are approximately 2 of these cells per organism and their somas are found in the metathoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN16B121 group with ipsilateral arbors in a single VNC neuromere (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 16B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the T1 leg neuropil and sends output to the T1 leg neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There are approximately 5 of these cells per organism and their somas are found in the prothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN16B122 group with ipsilateral arbors in a single VNC neuromere (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 16B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the T1 leg neuropil and sends output to the T1 leg neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There are approximately 3 of these cells per organism and their somas are found in the prothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN16B123 group with ipsilateral arbors in a single VNC neuromere (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 16B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the T1 leg neuropil and sends output to the T1 leg neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There is approximately one of these cells per organism with its soma in the prothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN16B124 group with ipsilateral arbors in a single VNC neuromere (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 16B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the T1 leg neuropil and sends output to the T1 leg neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There are approximately 2 of these cells per organism and their somas are found in the prothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN16B125 group with ipsilateral arbors in a single VNC neuromere (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 16B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the T2 leg neuropil and sends output to the T2 leg neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There are approximately 6 of these cells per organism and their somas are found in the mesothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Any neuroblast NB1-1 (FBbt:00001371) that is part of some labial segment (FBbt:00000014).
Motor neuron that innervates the internal dorsal acute muscle 1 of larval abdominal segments A1 to A7. Its dendritic arborization occupies the lateral domain of the ventral nerve cord neuropil. It exits the ventral nerve cord via the anterior root of the intersegmental nerve and innervates the DA1 muscle with type Ib boutons (Landgraf et al., 1997; Hoang and Chiba, 2001). By embryonic stage 16, it has a short contralaterally projecting neurite extending into the posterior commissure.
Any larval A-subperineurial glial cell (FBbt:00001259) that is part of some larval abdominal 1 neuromere (FBbt:00111033).
Any larval B-subperineurial glial cell (FBbt:00001276) that is part of some larval abdominal 1 neuromere (FBbt:00111033).
Any pCC neuron (FBbt:00001448) that has its soma located in some cell body rind of larval abdominal 1 neuromere (FBbt:00051990).
Any larval A-subperineurial glial cell (FBbt:00001259) that is part of some larval abdominal 2 neuromere (FBbt:00111034).
Any larval B-subperineurial glial cell (FBbt:00001276) that is part of some larval abdominal 2 neuromere (FBbt:00111034).
Any pCC neuron (FBbt:00001448) that has its soma located in some cell body rind of larval abdominal 2 neuromere (FBbt:00051991).
Any larval A-subperineurial glial cell (FBbt:00001259) that is part of some larval abdominal 3 neuromere (FBbt:00111035).
Any larval B-subperineurial glial cell (FBbt:00001276) that is part of some larval abdominal 3 neuromere (FBbt:00111035).
Any pCC neuron (FBbt:00001448) that has its soma located in some cell body rind of larval abdominal 3 neuromere (FBbt:00051992).
Any larval A-subperineurial glial cell (FBbt:00001259) that is part of some larval abdominal 4 neuromere (FBbt:00111036).
Any larval B-subperineurial glial cell (FBbt:00001276) that is part of some larval abdominal 4 neuromere (FBbt:00111036).
Any pCC neuron (FBbt:00001448) that has its soma located in some cell body rind of larval abdominal 4 neuromere (FBbt:00051993).
Any larval A-subperineurial glial cell (FBbt:00001259) that is part of some larval abdominal 5 neuromere (FBbt:00111037).
Any larval B-subperineurial glial cell (FBbt:00001276) that is part of some larval abdominal 5 neuromere (FBbt:00111037).
Any pCC neuron (FBbt:00001448) that has its soma located in some cell body rind of larval abdominal 5 neuromere (FBbt:00051994).
Any larval A-subperineurial glial cell (FBbt:00001259) that is part of some larval abdominal 6 neuromere (FBbt:00111038).
Any larval B-subperineurial glial cell (FBbt:00001276) that is part of some larval abdominal 6 neuromere (FBbt:00111038).
Any pCC neuron (FBbt:00001448) that has its soma located in some cell body rind of larval abdominal 6 neuromere (FBbt:00051995).
Any larval A-subperineurial glial cell (FBbt:00001259) that is part of some larval abdominal 7 neuromere (FBbt:00111039).
Any larval B-subperineurial glial cell (FBbt:00001276) that is part of some larval abdominal 7 neuromere (FBbt:00111039).
Any larval A-subperineurial glial cell (FBbt:00001259) that is part of some larval abdominal 8 neuromere (FBbt:00111040).
Any larval B-subperineurial glial cell (FBbt:00001276) that is part of some larval abdominal 8 neuromere (FBbt:00111040).
A-subperineurial glial cell located in an abdominal neuromere. It is found near the anterior border of its neuromere, around 20-30% along the medio-lateral axis (Ito et al., 1995). It develops from neuroblast NB1-1 of the abdomen (Beckervordersandforth et al., 2008).
Larval primary interneuron that develops from an abdominal neuroblast NB1-1. It projects ipsilaterally (Bossing et al., 1996).
Large subperineural glial cell that sits over the posterior commissure just medial to the longitudinal connectives (Klambt and Goodman, 1991; Ito et al., 1995). It sends processes in three directions: medially to the midline, anteriorly and posteriorly (Ito et al., 1995). Unlike the A-subperineural glial cell, the B-subperineural glial cell is only found in abdominal neuromeres, and lies at approximately the center of the segment along the antero-posterior axis (Ito et al., 1995). It develops from neuroblast NB1-1 of the abdomen (Beckervordersandforth et al., 2008).
Motor neuron that is born from the first GMC to bud from neuroblast NB1-1 (GMC1-1a) in thoracic and abdominal segments and is part of the Notch OFF hemilineage (Skeath and Doe, 1998). It has a large round cell body that sits at the dorsal surface of the CNS, in the next anterior segment to the muscle it innervates, just posterior to the posterior commissure and longitudinal connective (Schmid et al., 1999; Zarin and Labrador, 2019). It innervates dorsal acute muscle 1 (DA1; muscle 1) (Landgraf et al., 1997). It expresses even-skipped (Manning et al., 2012).
Larval DA1 motor neuron with its soma in the abdominal 1 neuromere. It crosses the segment boundary and innervates musculature in the abdominal 2 segment. It forms type Ib synapses to a muscle cell of abdominal 2 dorsal acute muscle 1.
Larval DA1 motor neuron with its soma in the abdominal 2 neuromere. It crosses the segment boundary and innervates musculature in the abdominal 3 segment. It forms type Ib synapses to a muscle cell of abdominal 3 dorsal acute muscle 1.
Larval DA1 motor neuron with its soma in the abdominal 3 neuromere. It crosses the segment boundary and innervates musculature in the abdominal 4 segment. It forms type Ib synapses to a muscle cell of abdominal 4 dorsal acute muscle 1.
Larval DA1 motor neuron with its soma in the abdominal 4 neuromere. It crosses the segment boundary and innervates musculature in the abdominal 5 segment. It forms type Ib synapses to a muscle cell of abdominal 5 dorsal acute muscle 1.
Larval DA1 motor neuron with its soma in the abdominal 5 neuromere. It crosses the segment boundary and innervates musculature in the abdominal 6 segment. It forms type Ib synapses to a muscle cell of abdominal 6 dorsal acute muscle 1.
Larval DA1 motor neuron with its soma in the abdominal 6 neuromere. It crosses the segment boundary and innervates musculature in the abdominal 7 segment. It forms type Ib synapses to a muscle cell of abdominal 7 dorsal acute muscle 1.
Larval DA1 motor neuron with its soma in the mesothoracic neuromere. It crosses the segment boundary and innervates musculature in the metathoracic segment. It forms type Ib synapses to a muscle cell of metathoracic dorsal acute muscle 1.
Larval DA1 motor neuron with its soma in the metathoracic neuromere. It crosses the segment boundary and innervates musculature in the abdominal 1 segment. It forms type Ib synapses to a muscle cell of abdominal 1 dorsal acute muscle 1.
Larval DA1 motor neuron with its soma in the prothoracic neuromere. It crosses the segment boundary and innervates musculature in the mesothoracic segment. It forms type Ib synapses to a muscle cell of mesothoracic dorsal acute muscle 1.
Any pCC neuron (FBbt:00001448) that has its soma located in some cell body rind of larval mesothoracic neuromere (FBbt:00051988).
Any pCC neuron (FBbt:00001448) that has its soma located in some cell body rind of larval metathoracic neuromere (FBbt:00051989).
Larval primary motor neuron that develops from neuroblast NB1-1 and fasciculates with the segmental nerve (Bossing et al., 1996). It is the second motor neuron to arise from NB1-1 and is only found in thoracic segments (Bossing et al., 1996; Rickert et al., 2018). Its axon terminates amongst ventrolateral muscles without a detectable end-plate (Bossing et al., 1996).
Posterior corner cell (pCC) of the larva. It is born from the first GMC to bud from neuroblast NB1-1 (GMC1-1a) and is part of the Notch ON hemilineage (Skeath and Doe, 1998). It extends a neurite anteriorly along one a longitudinal fascicles (Doe et al., 1988). It expresses even-skipped (Manning et al., 2012).
Any pCC neuron (FBbt:00001448) that has its soma located in some cell body rind of larval prothoracic neuromere (FBbt:00051987).
Larval primary interneuron that develops from a thoracic neuroblast NB1-1. It projects ipsilaterally (Bossing et al., 1996).
Lateral ventral subperineurial glial cell of an abdominal segment. it lies 0-10% along the antero-posterior axis and 60-90% along the medio-lateral axis (Ito et al., 1995) and develops from neuroblast NB1-1 of the abdomen (Beckervordersandforth et al., 2008).
Any neuron that develops from neuroblast NB1-1 during the postembryonic phase of neurogenesis. These are all Notch OFF hemilineage neurons, as the Notch ON hemilineage is eliminated by apoptosis (Lacin et al., 2019). In the adult, these neurons are glutamatergic (Lacin et al., 2019).
Any primary interneuron (FBbt:00052517) that develops from some neuroblast NB1-1 (FBbt:00001371).
Any primary motor neuron (FBbt:00052518) that develops from some neuroblast NB1-1 (FBbt:00001371).
Any neuroblast NB1-1 (FBbt:00001371) that is part of some maxillary segment (FBbt:00000013).
Any neuron that develops from neuroblast NB1-1 at any stage of life.
Any neuron that develops from neuroblast NB1-1 during the embryonic phase of neurogenesis.
Interneuron that is born from the first GMC to bud from neuroblast NB1-1 (GMC1-1a) and is part of the Notch ON hemilineage (Skeath and Doe, 1998). Its large, round cell body is located just posterior, medial and ventral to its sibling, the MN-DA1 (aCC) motor neuron (FBbt:00001447). It extends a neurite anteriorly along one of the longitudinal fascicles (Doe et al., 1988). It expresses even-skipped (Manning et al., 2012).
Neuroblast NB1-1 found in a thoracic segment. During embryonic development, it generates the CoA motorneuron in addition to aCC (DA1) (Schmid et al., 1999), but does not generate glia (Schmid et al., 1999; Beckervordersandforth et al., 2008). It resumes proliferation in the larva in all thoracic segments to generate postembryonic lineage 16 (Lacin and Truman, 2016).