abdominal neuroblast NB7-2 [FBbt_00052489]
Any neuroblast NB7-2 (FBbt:00001392) that is part of some abdominal segment (FBbt:00000021).
Any neuroblast NB7-2 (FBbt:00001392) that is part of some abdominal segment (FBbt:00000021).
Adult ascending neuron of the AN11B008 group with ipsilateral VNC arbors (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 11B 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 tract of dorsal cervical fasciculus I (Takemura et al., 2024; Marin et al., 2024). It receives input in the T1 leg neuropil and neck neuropil and sends output to the neck neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is gaba (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 AN11B012 group with ipsilateral VNC arbors (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 11B 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 tract of dorsal cervical fasciculus I (Takemura et al., 2024; Marin et al., 2024). It receives input in the intermediate tectulum and neck neuropil and sends output to the neck neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is gaba (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 hemilineage A (Notch ON) neuron that develops from neuroblast NB7-2 during the postembryonic phase of neurogenesis. In the adult, these neurons are cholinergic (Lacin et al., 2019).
Any hemilineage B (Notch OFF) neuron that develops from neuroblast NB7-2 during the postembryonic phase of neurogenesis. In the adult, these neurons are GABAergic (Lacin et al., 2019).
Adult intrinsic neuron of the IN11A001 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a primary neuron of the 11A 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 gaba (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 IN11A002 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 11A 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 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 IN11A003 group with ipsilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 11A 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 8 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 IN11A004 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 11A 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 prothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN11A005 group (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 11A 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 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 IN11A006 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 11A 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 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 intrinsic neuron of the IN11A007 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 11A hemilineage (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 prothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN11A008 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 11A 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 acetylcholine (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 IN11A009 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 11A 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 prothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN11A010 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 11A hemilineage (Takemura et al., 2024; Marin et al., 2024). It sends output to the T1 leg neuropil and lower tectulum (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (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 IN11A011 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 11A hemilineage (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 prothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN11A012 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 11A 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 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 intrinsic neuron of the IN11A013 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 11A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the 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 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 IN11A014 group (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 11A 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 acetylcholine (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 IN11A015 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 11A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the intermediate tectulum and lower tectulum and sends output to the 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 mesothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN11A016 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 11A 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 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 IN11A017 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 11A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in multiple regions and sends output to the T1 leg neuropil and lower 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 prothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN11A018 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 11A hemilineage (Takemura et al., 2024; Marin et al., 2024). It sends output to the upper 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 prothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN11A019 group with ipsilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 11A 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 IN11A020 group (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 11A hemilineage (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 prothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN11A021 group (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 11A hemilineage (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 prothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN11A022 group with ipsilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 11A 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 acetylcholine (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 IN11A023 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 11A 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 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 IN11A025 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 11A 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 acetylcholine (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 IN11A026 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 11A 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 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 IN11A027 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 11A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the intermediate tectulum and lower tectulum (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 (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN11A028 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 11A hemilineage (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 IN11A030 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 11A 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 acetylcholine (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 IN11A031 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 11A 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 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 IN11A032 group (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 11A 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 (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN11A034 group with ipsilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 11A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the intermediate tectulum and neck neuropil and sends output to the haltere 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 prothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN11A035 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 11A 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 mesothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN11A036 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 11A 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 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 IN11A037 group with ipsilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 11A 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 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 IN11A040 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 11A 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 acetylcholine (Eckstein et al., 2024). There are approximately 3 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 IN11A041 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 11A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the lower tectulum and sends output to the T3 leg neuropil and lower tectulum (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (Eckstein et al., 2024). There are approximately 3 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 IN11A042 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 11A 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 IN11A043 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 11A 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 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 intrinsic neuron of the IN11A045 group with ipsilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 11A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the haltere neuropil and sends output to the haltere neuropil and neck 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 IN11B001 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a primary neuron of the 11B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the wing neuropil and 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 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 IN11B002 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 11B 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 gaba (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 IN11B003 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 11B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the wing 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 mesothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN11B004 group (Takemura et al., 2024; Marin et al., 2024). It belongs to the 11B hemilineage (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is gaba (Eckstein et al., 2024). There are approximately 18 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 IN11B005 group with ipsilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 11B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the intermediate tectulum and wing neuropil and sends output to the T3 leg neuropil and abdominal neuromere (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is gaba (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 IN11B006 group with ipsilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a primary neuron of the 11B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the T3 leg neuropil and sends output to the upper tectulum (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is gaba (Eckstein et al., 2024). There are approximately 2 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 IN11B009 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 11B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the tectulum and sends output to the upper tectulum (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is gaba (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 IN11B011 group with ipsilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 11B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the intermediate tectulum and neck neuropil and sends output to multiple regions (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is gaba (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 IN11B012 group with ipsilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 11B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in multiple regions and sends output to the haltere neuropil and tectulum (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is gaba (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 IN11B013 group (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 11B hemilineage (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is gaba (Eckstein et al., 2024). There are approximately 10 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 IN11B014 group (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 11B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the tectulum 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 IN11B015 group (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 11B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the tectulum and sends output to the tectulum (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is gaba (Eckstein et al., 2024). There are approximately 8 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 IN11B016 group (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 11B 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 gaba (Eckstein et al., 2024). There are approximately 12 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 IN11B017 group (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 11B 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 gaba (Eckstein et al., 2024). There are approximately 13 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 IN11B018 group with ipsilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 11B hemilineage (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 and prothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN11B019 group (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 11B 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 gaba (Eckstein et al., 2024). There are approximately 9 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 IN11B020 group (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 11B hemilineage (Takemura et al., 2024; Marin et al., 2024). It sends output to the wing neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is gaba (Eckstein et al., 2024). There are approximately 9 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 IN11B021 group (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 11B 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 gaba (Eckstein et al., 2024). There are approximately 14 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 IN11B022 group (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 11B hemilineage (Takemura et al., 2024; Marin et al., 2024). It sends output to the haltere neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is gaba (Eckstein et al., 2024). There are approximately 19 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 IN11B023 group with ipsilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 11B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the haltere neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is gaba (Eckstein et al., 2024). There are approximately 9 of these cells per organism and their somas are found in the mesothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Any neuroblast NB7-2 (FBbt:00001392) that is part of some labial segment (FBbt:00000014).
Any larval T11v neuron (FBbt:00048690) that has its soma located in some cell body rind of larval mesothoracic neuromere (FBbt:00051988).
Any larval T11v neuron (FBbt:00048690) that has its soma located in some cell body rind of larval metathoracic neuromere (FBbt:00051989).
Larval primary interneuron that develops from NB7-2 and projects contralaterally, via the posterior commissure (Bossing et al., 1996).
Larval ipsilateral primary interneuron that develops from NB7-2 (Bossing et al., 1996). It extends posteriorly (Bossing et al., 1996).
Larval thoracic interneuron that is part of lineage 11 (Zwart et al., 2016). Its soma is located laterally and its neurite extends dorsomedially (Zwart et al., 2016).
Any neuron that develops from neuroblast NB7-2 during the postembryonic phase of neurogenesis. Both hemilineages survive and signal via different neurotransmitters (Lacin et al., 2019).
Any primary interneuron (FBbt:00052517) that develops from some neuroblast NB7-2 (FBbt:00001392).
Any neuroblast NB7-2 (FBbt:00001392) that is part of some mandibular segment (FBbt:00000012).
Any neuroblast NB7-2 (FBbt:00001392) that is part of some maxillary segment (FBbt:00000013).
Any neuroblast NB7-2 (FBbt:00001392) that is part of some mesothoracic segment (FBbt:00000018).
Any neuroblast NB7-2 (FBbt:00001392) that is part of some metathoracic segment (FBbt:00000019).
Any neuron that develops from neuroblast NB7-2 at any stage of life.
Any neuron that develops from neuroblast NB7-2 during the embryonic phase of neurogenesis.
Unilateral neuron of the NUI002 group of the adult ventral nerve cord that primarily arborizes in the neck neuropil (Ehrhardt et al., 2023). It is an intersegmental interneuron (Ehrhardt et al., 2023). It has dendritic arborization in the ipsilateral neck neuropil (Ehrhardt et al., 2023). It has axonal arborization in the ipsilateral haltere neuropil (Ehrhardt et al., 2023). It has partitioned arborization in the ipsilateral wing neuropil and intermediate tectulum of the mesothoracic neuromere, where dendritic and axonal arbors occupy separate regions of the neuropil (Ehrhardt et al., 2023). It has its soma in a posterior-dorsal-lateral position in the prothoracic neuromere (Ehrhardt et al., 2023). It belongs to the 11B hemilineage of the T1 neuromere (Ehrhardt et al., 2023). There are five of these cells per hemineuromere (Ehrhardt et al., 2023).
Any neuroblast NB7-2 (FBbt:00001392) that is part of some prothoracic segment (FBbt:00000017).
Any neuroblast NB7-2 (FBbt:00001392) that is part of some thoracic segment (FBbt:00000016).
Bilateral neuron of the WBI017 group of the adult ventral nerve cord that primarily arborizes in the wing neuropil (Ehrhardt et al., 2023). It is an intersegmental interneuron (Ehrhardt et al., 2023). It has dendritic arborization in the ipsilateral intermediate tectulum of the mesothoracic neuromere (Ehrhardt et al., 2023). It has axonal arborization in the ipsilateral haltere neuropil and the contralateral haltere neuropil (Ehrhardt et al., 2023). It has mixed arborization in the ipsilateral wing neuropil and the contralateral wing neuropil (Ehrhardt et al., 2023). It has its soma in a posterior-dorsal-lateral position in the prothoracic neuromere (Ehrhardt et al., 2023). It belongs to the 11B hemilineage of the T1 neuromere (Ehrhardt et al., 2023). There is one of these cells per hemineuromere (Ehrhardt et al., 2023).
Bilateral neuron of the WBI018 group of the adult ventral nerve cord that primarily arborizes in the wing neuropil (Ehrhardt et al., 2023). It is an intersegmental interneuron (Ehrhardt et al., 2023). It has dendritic arborization in the ipsilateral wing neuropil (Ehrhardt et al., 2023). It has axonal arborization in the ipsilateral haltere neuropil and the contralateral haltere neuropil (Ehrhardt et al., 2023). It has its soma in a anterior-dorsal-lateral position in the mesothoracic neuromere (Ehrhardt et al., 2023). It belongs to the 11B hemilineage of the T2 neuromere (Ehrhardt et al., 2023).
Bilateral neuron of the WBI019 group of the adult ventral nerve cord that primarily arborizes in the wing neuropil (Ehrhardt et al., 2023). It is an intersegmental interneuron (Ehrhardt et al., 2023). It has dendritic arborization in the contralateral wing neuropil (Ehrhardt et al., 2023). It has axonal arborization in the ipsilateral haltere neuropil and the contralateral haltere neuropil (Ehrhardt et al., 2023). It has mixed arborization in the ipsilateral wing neuropil (Ehrhardt et al., 2023). It has its soma in a posterior-dorsal-medial position in the mesothoracic neuromere (Ehrhardt et al., 2023). It belongs to the 11B hemilineage of the T2 neuromere (Ehrhardt et al., 2023).
Unilateral neuron of the WUL003 group of the adult ventral nerve cord that primarily arborizes in the wing 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 wing neuropil (Ehrhardt et al., 2023). It has its soma in a anterior-dorsal-lateral position in the mesothoracic neuromere (Ehrhardt et al., 2023). It belongs to the 11B hemilineage of the T2 neuromere (Ehrhardt et al., 2023). There is one of these cells per hemineuromere (Ehrhardt et al., 2023).
Unilateral neuron of the WUL004 group of the adult ventral nerve cord that primarily arborizes in the wing 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 wing neuropil (Ehrhardt et al., 2023). It has its soma in a anterior-dorsal-lateral position in the mesothoracic neuromere (Ehrhardt et al., 2023). It belongs to the 11B hemilineage of the T2 neuromere (Ehrhardt et al., 2023). There is one of these cells per hemineuromere (Ehrhardt et al., 2023).
Unilateral neuron of the WUL005 group of the adult ventral nerve cord that primarily arborizes in the wing 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 wing neuropil (Ehrhardt et al., 2023). It has its soma in a posterior-dorsal-lateral position in the mesothoracic neuromere (Ehrhardt et al., 2023). It belongs to the 11B hemilineage of the T2 neuromere (Ehrhardt et al., 2023). There is one of these cells per hemineuromere (Ehrhardt et al., 2023).
Unilateral neuron of the WUL006 group of the adult ventral nerve cord that primarily arborizes in the wing 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 wing neuropil and intermediate tectulum of the mesothoracic neuromere (Ehrhardt et al., 2023). It has its soma in a posterior-dorsal-medial position in the mesothoracic neuromere (Ehrhardt et al., 2023). It belongs to the 11B hemilineage of the T2 neuromere (Ehrhardt et al., 2023). There is one of these cells per hemineuromere (Ehrhardt et al., 2023).
Unilateral neuron of the WUL013 group of the adult ventral nerve cord that primarily arborizes in the wing 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 wing neuropil and intermediate tectulum of the mesothoracic neuromere (Ehrhardt et al., 2023). It has its soma in a posterior-dorsal-lateral position in the mesothoracic neuromere (Ehrhardt et al., 2023). It belongs to the 11B hemilineage of the T2 neuromere (Ehrhardt et al., 2023). There is one of these cells per hemineuromere (Ehrhardt et al., 2023).
Unilateral neuron of the WUL014 group of the adult ventral nerve cord that primarily arborizes in the wing 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 wing neuropil and intermediate tectulum of the mesothoracic neuromere (Ehrhardt et al., 2023). It has its soma in a posterior-dorsal-medial position in the mesothoracic neuromere (Ehrhardt et al., 2023). It belongs to the 11B hemilineage of the T2 neuromere (Ehrhardt et al., 2023). There is one of these cells per hemineuromere (Ehrhardt et al., 2023).