abdominal neuroblast NB2-2 [FBbt_00001387]
Neuroblast NB2-2 found in an abdominal segment. It does not produce a secondary lineage (Lacin and Truman, 2016).
Neuroblast NB2-2 found in an abdominal segment. It does not produce a secondary lineage (Lacin and Truman, 2016).
Adult cholinergic interneuron of hemilineage 10B with its soma in the prothoracic neuromere that receives input from a directionally-tuned femoral chordotonal organ (FeCO) club neuron and responds to tibial vibrations and tibial movements in both directions (Agrawal et al., 2020). These cells innervate multiple neuromeres and a subset ascend to the brain, where they innervate the antennal mechanosensory and motor center (Agrawal et al., 2020). Its activation causes pausing behaviour in walking flies (Agrawal et al., 2020).
Adult ascending neuron of the AN10B005 group with bilateral VNC arbors (Takemura et al., 2024; Marin et al., 2024). It is a primary neuron of the 10B 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). It receives input in multiple regions and sends output to the brain (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (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 AN10B008 group with bilateral VNC arbors (Takemura et al., 2024; Marin et al., 2024). It is a primary neuron of the 10B 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 multiple regions and sends output to multiple regions (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (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 ascending neuron of the AN10B009 group with bilateral VNC arbors (Takemura et al., 2024; Marin et al., 2024). It is a primary neuron of the 10B 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 ventral lateral tract of ventral cervical fasciculus (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 acetylcholine (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 ascending neuron of the AN10B015 group with bilateral VNC arbors (Takemura et al., 2024; Marin et al., 2024). It is a primary neuron of the 10B 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). It receives input in multiple regions and sends output to multiple regions (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (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 ascending neuron of the AN10B017 group with bilateral VNC arbors (Takemura et al., 2024; Marin et al., 2024). It is a primary neuron of the 10B 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 acetylcholine (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 ascending neuron of the AN10B018 group with bilateral VNC arbors (Takemura et al., 2024; Marin et al., 2024). It is a primary neuron of the 10B 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 median dorsal abdominal tract (Takemura et al., 2024; Marin et al., 2024). It receives input in the T3 leg neuropil and sends output to the T3 leg neuropil and tectulum (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (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 ascending neuron of the AN10B019 group with bilateral VNC arbors (Takemura et al., 2024; Marin et al., 2024). It is a primary neuron of the 10B 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 dorsal lateral tract of ventral cervical fasciculus (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 acetylcholine (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 ascending neuron of the AN10B020 group with bilateral VNC arbors (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 10B 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 dorsal lateral tract of ventral cervical fasciculus (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 acetylcholine (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 ascending neuron of the AN10B021 group with bilateral VNC arbors (Takemura et al., 2024; Marin et al., 2024). It is a primary neuron of the 10B 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 median dorsal abdominal tract (Takemura et al., 2024; Marin et al., 2024). It receives input in the T2 leg neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (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 ascending neuron of the AN10B022 group with bilateral VNC arbors (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 10B 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 dorsal lateral tract of ventral cervical fasciculus (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 acetylcholine (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 ascending neuron of the AN10B024 group with bilateral VNC arbors (Takemura et al., 2024; Marin et al., 2024). It is a primary neuron of the 10B 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). It receives input in the leg neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (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 ascending neuron of the AN10B026 group with bilateral VNC arbors (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 10B 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). 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 acetylcholine (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 AN10B027 group with contralateral arbors in the VNC (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 10B 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 dorsal lateral tract of ventral cervical fasciculus (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 acetylcholine (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 ascending neuron of the AN10B029 group with bilateral VNC arbors (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 10B 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 dorsal lateral tract of ventral cervical fasciculus (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (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 ascending neuron of the AN10B031 group with bilateral VNC arbors (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 10B 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 dorsal lateral tract of ventral cervical fasciculus (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 acetylcholine (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 AN10B033 group with bilateral VNC arbors (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 10B 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 dorsal lateral tract of ventral cervical fasciculus (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 acetylcholine (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 ascending neuron of the AN10B034 group with bilateral VNC arbors (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 10B 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 dorsal lateral tract of ventral cervical fasciculus (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (Eckstein et al., 2024). There are approximately 10 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 ascending neuron of the AN10B035 group with bilateral VNC arbors (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 10B 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 dorsal lateral tract of ventral cervical fasciculus (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (Eckstein et al., 2024). There are approximately 11 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 ascending neuron of the AN10B037 group with bilateral VNC arbors (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 10B 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 dorsal lateral tract of ventral cervical fasciculus (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (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 ascending neuron of the AN10B039 group with bilateral VNC arbors (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 10B 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 dorsal lateral tract of ventral cervical fasciculus (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (Eckstein et al., 2024). There are approximately 10 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 ascending neuron of the AN10B045 group with bilateral VNC arbors (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 10B hemilineage (Takemura et al., 2024; Marin et al., 2024). Within the VNC it fasciculates with the dorsal lateral tract of ventral cervical fasciculus (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (Eckstein et al., 2024). There are approximately 10 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 ascending neuron of the AN10B046 group with bilateral VNC arbors (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 10B 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 dorsal lateral tract of ventral cervical fasciculus (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (Eckstein et al., 2024). There are approximately 14 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 ascending neuron of the AN10B047 group with bilateral VNC arbors (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 10B 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 dorsal lateral tract of ventral cervical fasciculus (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (Eckstein et al., 2024). There are approximately 14 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 ascending neuron of the AN10B048 group with bilateral VNC arbors (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 10B 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 dorsal lateral tract of ventral cervical fasciculus (Takemura et al., 2024; Marin et al., 2024). It sends output to the leg neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (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 ascending neuron of the AN10B049 group with bilateral VNC arbors (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 10B 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 dorsal lateral tract of ventral cervical fasciculus (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (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 ascending neuron of the AN10B051 group with bilateral VNC arbors (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 10B 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 dorsal lateral tract of ventral cervical fasciculus (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 acetylcholine (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 ascending neuron of the AN10B053 group with bilateral VNC arbors (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 10B 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 dorsal lateral tract of ventral cervical fasciculus (Takemura et al., 2024; Marin et al., 2024). It sends output to the leg neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (Eckstein et al., 2024). There are approximately 10 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 ascending neuron of the AN10B056 group with bilateral VNC arbors (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 10B 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 dorsal lateral tract of ventral cervical fasciculus (Takemura et al., 2024; Marin et al., 2024). It sends output to the brain (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (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 AN10B060 group with bilateral VNC arbors (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 10B 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 dorsal lateral tract of ventral cervical fasciculus (Takemura et al., 2024; Marin et al., 2024). It receives input in the leg neuropil and sends output to multiple regions (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (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 ascending neuron of the AN10B061 group with bilateral VNC arbors (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 10B hemilineage (Takemura et al., 2024; Marin et al., 2024). Within the VNC it fasciculates with the dorsal lateral tract of ventral cervical fasciculus (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 acetylcholine (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 IN10B001 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a primary neuron of the 10B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the T1 leg neuropil and sends output to multiple regions (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (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 IN10B002 group with contralateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a primary neuron of the 10B 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 acetylcholine (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 IN10B003 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a primary neuron of the 10B hemilineage (Takemura et al., 2024; Marin et al., 2024). It sends output to the leg neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (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 IN10B004 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a primary neuron of the 10B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in multiple regions and sends output to the T1 leg neuropil and T3 leg neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (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 IN10B006 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a primary neuron of the 10B 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 acetylcholine (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 IN10B007 group (Takemura et al., 2024; Marin et al., 2024). It is a primary neuron of the 10B hemilineage (Takemura et al., 2024; Marin et al., 2024). It sends output to the leg neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (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 IN10B010 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a primary neuron of the 10B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in multiple regions and sends output to the abdominal neuromere (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (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 IN10B011 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a primary neuron of the 10B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in multiple regions and sends output to the abdominal neuromere (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (Eckstein et al., 2024). There are approximately 4 of these cells per organism and their somas are found in the abdominal neuromere and metathoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN10B012 group with bilateral arbors in a single VNC neuromere (Takemura et al., 2024; Marin et al., 2024). It is a primary neuron of the 10B 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 acetylcholine (Eckstein et al., 2024). There are approximately 4 of these cells per organism and their somas are found in the metathoracic neuromere and prothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN10B013 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a primary neuron of the 10B hemilineage (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (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 IN10B014 group (Takemura et al., 2024; Marin et al., 2024). It is a primary neuron of the 10B 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 acetylcholine (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 IN10B016 group with contralateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a primary neuron of the 10B 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 and abdominal neuromere (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (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 IN10B023 group (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 10B 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 acetylcholine (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 IN10B025 group (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 10B 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 acetylcholine (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 IN10B028 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 10B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the medial ventral association center (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (Eckstein et al., 2024). There are approximately 10 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 IN10B030 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 10B hemilineage (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (Eckstein et al., 2024). There are approximately 8 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 IN10B031 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 10B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the leg neuropil and sends output to multiple regions (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (Eckstein et al., 2024). There are approximately 5 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 IN10B032 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 10B hemilineage (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (Eckstein et al., 2024). There are approximately 20 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 IN10B033 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 10B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the leg neuropil and medial ventral association center and sends output to the leg neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (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 IN10B034 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 10B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the T1 leg neuropil and lower tectulum and sends output to multiple regions (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (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 IN10B036 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 10B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the leg neuropil and sends output to multiple regions (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (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 IN10B038 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 10B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the leg neuropil and sends output to multiple regions (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (Eckstein et al., 2024). There are approximately 9 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 IN10B040 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 10B hemilineage (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (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 IN10B041 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 10B hemilineage (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (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 IN10B042 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 10B hemilineage (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (Eckstein et al., 2024). There are approximately 20 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 IN10B043 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 10B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the medial ventral association center and sends output to the medial ventral association center (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (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 IN10B044 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 10B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the medial ventral association center (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (Eckstein et al., 2024). There are approximately 8 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 IN10B050 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 10B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the medial ventral association center and sends output to the leg neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (Eckstein et al., 2024). There are approximately 10 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 IN10B052 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 10B hemilineage (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (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 IN10B054 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 10B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the medial ventral association center (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (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 IN10B055 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 10B hemilineage (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (Eckstein et al., 2024). There are approximately 16 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 IN10B057 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 10B 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 acetylcholine (Eckstein et al., 2024). There are approximately 29 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 IN10B058 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 10B hemilineage (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (Eckstein et al., 2024). There are approximately 22 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 IN10B059 group (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 10B 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 acetylcholine (Eckstein et al., 2024). There are approximately 13 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 IN10B061 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 10B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the T1 leg neuropil and sends output to multiple regions (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (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).
Any neuroblast NB2-2 (FBbt:00001385) that is part of some labial segment (FBbt:00000014).
Larval LT1/LT2 motor neuron that innervates the LT1 and LT2 muscles of an abdominal 1-7 segment. It fasciculates with the SNa nerve branch and innervates muscles in the same segment as its soma (Landgraf et al., 1997; Schmid et al, 1999; Hoang and Chiba, 2001; Kim et al., 2009).
Larval LT2/LT3 motor neuron that innervates the LT2 and LT3 muscles of an abdominal 1-7 segment. It fasciculates with the SNa nerve branch and innervates muscles in the same segment as its soma (Landgraf et al., 1997; Schmid et al, 1999; Hoang and Chiba, 2001; Kim et al., 2009).
Premotor neuron of the larval abdominal neuromere that is part of lineage 10 (Zarin et al., 2019). Its primary neurite extends dorsomedially and anteriorly arborizing across the midline. It receives strong input from the class IV dendritic arborizing neurons (Ohyama et al., 2015; Gerhard et al., 2017) and the class III dendritic arborizing neurons (Jovanic et al., 2019).
Larval premotor neuron that is part of lineage 10 (Zarin et al., 2019). Its soma is found ventrally and its neurite extends dorsally, before branching, all three main branches extend anteriorly, with one crossing the midline and one extending (ipsi)laterally (Zwart et al., 2016; Zarin et al., 2019).
Neuron of the larval abdominal neuromere that is part of lineage 10. Its primary neurite extends dorsomedially arborizing across the midline, with both dendritic and axonal domains extending anteroposteriorly. It receives input from Basin-2 (Ohyama et al., 2015). This is a nociceptive integrator neuron, i.e. it is a node of convergence for multiple neurons carrying nociceptive information (Burgos et al., 2018).
Ascending neuron of the larval abdominal neuromere that is part of lineage 10. Its primary neurite extends dorsomedially, arborizing close to and across the midline. It then extends anteriorly to terminate in the contralateral brain lobe. It receives strong input from Basin-2 and the mechanosensory chordotonal neurons (Ohyama et al., 2015).
Neuron of the larval abdominal neuromere that is part of lineage 10. It is a small neuron that arborizes close to or across the midline. It receives input from Basin neurons (Ohyama et al., 2015).
Any larval A10a neuron (FBbt:00111253) that has its soma located in some cell body rind of larval abdominal 1 neuromere (FBbt:00051990).
Any larval A10e neuron (FBbt:00048702) that has its soma located in some cell body rind of larval abdominal 1 neuromere (FBbt:00051990).
Any larval A10j neuron (FBbt:00111260) that has its soma located in some cell body rind of larval abdominal 1 neuromere (FBbt:00051990).
Any larval A10a neuron (FBbt:00111253) that has its soma located in some cell body rind of larval abdominal 2 neuromere (FBbt:00051991).
Any larval A10e neuron (FBbt:00048702) that has its soma located in some cell body rind of larval abdominal 2 neuromere (FBbt:00051991).
Any larval A10f neuron (FBbt:00111254) that has its soma located in some cell body rind of larval abdominal 2 neuromere (FBbt:00051991).
Any larval A10j neuron (FBbt:00111260) that has its soma located in some cell body rind of larval abdominal 2 neuromere (FBbt:00051991).
Any larval A10l neuron (FBbt:00111255) that has its soma located in some cell body rind of larval abdominal 2 neuromere (FBbt:00051991).
Any larval A10a neuron (FBbt:00111253) that has its soma located in some cell body rind of larval abdominal 3 neuromere (FBbt:00051992).
Any larval A10j neuron (FBbt:00111260) that has its soma located in some cell body rind of larval abdominal 3 neuromere (FBbt:00051992).
Larval primary interneuron that develops from NB2-2 of the abdomen. There are about 10 of these cells and they form a bundle that projects through the anterior commissure (Bossing et al., 1996). Compared to the thoracic NB2-2 interneurons, this contralateral bundle is more prominent and it makes an anterior turn after reaching the contralateral connective (Bossing et al., 1996).
Any primary motor neuron (FBbt:00052518) that has its soma located in some larval abdominal neuromere (FBbt:00111028) and develops from some neuroblast NB2-2 (FBbt:00001385).
Larval motor neuron that develops from NB2-2 and innervates the lateral transverse muscles 1 and 2 via type Ib boutons (Landgraf et al., 1997; Schmid et al, 1999; Hoang and Chiba, 2001; Kim et al., 2009). It has ipsilateral dendrites that extend anteriorly in the dorsolateral neuropil (Landgraf et al., 1997; Landgraf et al., 2003; Kim et al., 2009). Its axon fasciculates with the ipsilateral segmental nerve, innervating muscles of the same segment as its soma (Landgraf et al., 1997; Schmid et al, 1999; Hoang and Chiba, 2001; Kim et al., 2009).
Larval LT1/LT2 motor neuron with its soma in the abdominal 1 neuromere. It forms type Ib synapses to a muscle cell of abdominal 1 lateral transverse muscle 1 and a muscle cell of abdominal 1 lateral transverse muscle 2.
Larval LT1/LT2 motor neuron with its soma in the abdominal 2 neuromere. It forms type Ib synapses to a muscle cell of abdominal 2 lateral transverse muscle 1 and a muscle cell of abdominal 2 lateral transverse muscle 2.
Larval LT1/LT2 motor neuron with its soma in the abdominal 3 neuromere. It forms type Ib synapses to a muscle cell of abdominal 3 lateral transverse muscle 1 and a muscle cell of abdominal 3 lateral transverse muscle 2.
Larval LT1/LT2 motor neuron with its soma in the abdominal 4 neuromere. It forms type Ib synapses to a muscle cell of abdominal 4 lateral transverse muscle 1 and a muscle cell of abdominal 4 lateral transverse muscle 2.
Larval LT1/LT2 motor neuron with its soma in the abdominal 5 neuromere. It forms type Ib synapses to a muscle cell of abdominal 5 lateral transverse muscle 1 and a muscle cell of abdominal 5 lateral transverse muscle 2.
Larval LT1/LT2 motor neuron with its soma in the abdominal 6 neuromere. It forms type Ib synapses to a muscle cell of abdominal 6 lateral transverse muscle 1 and a muscle cell of abdominal 6 lateral transverse muscle 2.
Larval LT1/LT2 motor neuron with its soma in the abdominal 7 neuromere. It forms type Ib synapses to a muscle cell of abdominal 7 lateral transverse muscle 1 and a muscle cell of abdominal 7 lateral transverse muscle 2.
Larval motor neuron that develops from NB2-2 and innervates the lateral transverse muscles 2 and 3 via type Ib boutons (Landgraf et al., 1997; Schmid et al, 1999; Hoang and Chiba, 2001; Kim et al., 2009; Wang et al., 2022). It arborizes in the ipsilateral neuropil, and its axon fasciculates with the ipsilateral segmental nerve, innervating muscles of the same segment as its soma (Landgraf et al., 1997; Schmid et al, 1999; Hoang and Chiba, 2001; Kim et al., 2009).
Larval LT2/LT3 motor neuron with its soma in the abdominal 1 neuromere. It forms type Ib synapses to a muscle cell of abdominal 1 lateral transverse muscle 2 and a muscle cell of abdominal 1 lateral transverse muscle 3.
Larval LT2/LT3 motor neuron with its soma in the abdominal 2 neuromere. It forms type Ib synapses to a muscle cell of abdominal 2 lateral transverse muscle 2 and a muscle cell of abdominal 2 lateral transverse muscle 3.
Larval LT2/LT3 motor neuron with its soma in the abdominal 3 neuromere. It forms type Ib synapses to a muscle cell of abdominal 3 lateral transverse muscle 2 and a muscle cell of abdominal 3 lateral transverse muscle 3.
Larval LT2/LT3 motor neuron with its soma in the abdominal 4 neuromere. It forms type Ib synapses to a muscle cell of abdominal 4 lateral transverse muscle 2 and a muscle cell of abdominal 4 lateral transverse muscle 3.
Larval LT2/LT3 motor neuron with its soma in the abdominal 5 neuromere. It forms type Ib synapses to a muscle cell of abdominal 5 lateral transverse muscle 2 and a muscle cell of abdominal 5 lateral transverse muscle 3.
Larval LT2/LT3 motor neuron with its soma in the abdominal 6 neuromere. It forms type Ib synapses to a muscle cell of abdominal 6 lateral transverse muscle 2 and a muscle cell of abdominal 6 lateral transverse muscle 3.
Larval LT2/LT3 motor neuron with its soma in the abdominal 7 neuromere. It forms type Ib synapses to a muscle cell of abdominal 7 lateral transverse muscle 2 and a muscle cell of abdominal 7 lateral transverse muscle 3.
Any larval A-subperineurial glial cell (FBbt:00001259) that is part of some larval mesothoracic neuromere (FBbt:00111031).
Any larval A-subperineurial glial cell (FBbt:00001259) that is part of some larval metathoracic neuromere (FBbt:00111032).
Larval T10a neuron with its soma in the metathoracic neuromere (Gerhard et al., 2017).
Any larval T10g2 neuron (FBbt:00048689) that has its soma located in some cell body rind of larval metathoracic neuromere (FBbt:00051989).
Any larval A-subperineurial glial cell (FBbt:00001259) that is part of some larval prothoracic neuromere (FBbt:00111030).
Neuron with its cell body in a larval thoracic neuromere that may receive weak input from class IV dendritic arborizing neurons (Gerhard et al., 2017).
Larval thoracic interneuron that is part of lineage 10 (Zwart et al., 2016). Its soma is located ventrally and its neurite extends dorsally, then crosses the midline and arborizes contralaterally (Zwart et al., 2016).
A-subperineurial glial cell located in a thoracic 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 NB2-2 of the thorax (Beckervordersandforth et al., 2008).
Larval primary interneuron that develops from NB2-2 of the thorax. There are about 10 of these cells and they form a bundle that projects through the anterior commissure (Bossing et al., 1996). Compared to the abdominal NB2-2 interneurons, this contralateral bundle is less prominent and it does not make an anterior turn after reaching the contralateral connective (Bossing et al., 1996).
Any primary motor neuron (FBbt:00052518) that has its soma located in some cell body rind of larval thoracic neuromere (FBbt:00111265) and develops from some neuroblast NB2-2 (FBbt:00001385).
Any neuron that develops from neuroblast NB2-2 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 cholinergic (Lacin et al., 2019).
Any primary interneuron (FBbt:00052517) that develops from some neuroblast NB2-2 (FBbt:00001385).
Any primary motor neuron (FBbt:00052518) that develops from some neuroblast NB2-2 (FBbt:00001385).
Any neuroblast NB2-2 (FBbt:00001385) that is part of some mandibular segment (FBbt:00000012).
Any neuroblast NB2-2 (FBbt:00001385) that is part of some maxillary segment (FBbt:00000013).
Any neuron that develops from neuroblast NB2-2 at any stage of life.
Any neuron that develops from neuroblast NB2-2 during the embryonic phase of neurogenesis.
Neuroblast NB2-2 found in a thoracic segment. In the embryonic phase, it produces a subperineurial glial cell in addition to neurons (Schmid et al., 1999; Beckervordersandforth et al., 2008). In the larva, it resumes proliferation in all thoracic segments to produce postembryonic lineage 10 (Lacin and Truman, 2016).