abdominal 1 neuroblast NB5-2 [FBbt_00049167]
Any neuroblast NB5-2 (FBbt:00001376) that is part of some abdominal segment 1 (FBbt:00000022).
Any neuroblast NB5-2 (FBbt:00001376) that is part of some abdominal segment 1 (FBbt:00000022).
Any neuroblast NB5-2 (FBbt:00001376) that is part of some abdominal segment 2 (FBbt:00000023).
Any neuroblast NB5-2 (FBbt:00001376) that is part of some abdominal segment 3 (FBbt:00000024).
Any neuroblast NB5-2 (FBbt:00001376) that is part of some abdominal segment 4 (FBbt:00000025).
Any neuroblast NB5-2 (FBbt:00001376) that is part of some abdominal segment 5 (FBbt:00000026).
Any neuroblast NB5-2 (FBbt:00001376) that is part of some abdominal segment 6 (FBbt:00000027).
Any neuroblast NB5-2 (FBbt:00001376) that is part of some abdominal segment 7 (FBbt:00000028).
Any neuroblast NB5-2 (FBbt:00001376) that is part of some abdominal segment (FBbt:00000021).
Adult ascending neuron with contralateral arbors in the ventral nerve cord (VNC) (Takemura et al., 2024; Marin et al., 2024). It is a primary neuron of the NB5-2 Notch OFF (6B) hemilineage (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 and it exits the VNC via the cervical connective (Takemura et al., 2024; Marin et al., 2024). It receives input in and sends output to the contralateral prothoracic and mesothoracic neuromeres (Takemura et al., 2024; Marin et al., 2024; Sturner et al., 2025). It also receives input in the subesophageal zone (Sturner et al., 2025). 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 metathoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult ascending neuron of the AN06A010 group with bilateral VNC arbors (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A 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 haltere neuropil and neck neuropil and sends output to the haltere neuropil and 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 mesothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult ascending neuron of the AN06A015 group with bilateral VNC arbors (Takemura et al., 2024; Marin et al., 2024). It is a primary neuron of the 06A 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 sends output to the T1 leg neuropil and intermediate 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 prothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult ascending neuron of the AN06A016 group with bilateral VNC arbors (Takemura et al., 2024; Marin et al., 2024). It is a primary neuron of the 06A 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 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 AN06A017 group with bilateral VNC arbors (Takemura et al., 2024; Marin et al., 2024). It is a primary neuron of the 06A 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 upper tectulum 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 ascending neuron of the AN06A018 group with bilateral VNC arbors (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A 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 haltere neuropil and intermediate tectulum and sends output to the haltere neuropil and intermediate 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 prothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult ascending neuron of the AN06A026 group with bilateral VNC arbors (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A 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 haltere neuropil and neck neuropil and sends output to the haltere neuropil and neck neuropil (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 abdominal neuromere and metathoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult ascending neuron of the AN06A027 group with bilateral VNC arbors (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A 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 intermediate tectulum and neck neuropil and sends output to the intermediate tectulum and neck neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There are approximately 2 of these cells per organism and their somas are found in the prothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult ascending neuron of the AN06A030 group with bilateral VNC arbors (Takemura et al., 2024; Marin et al., 2024). It is a primary neuron of the 06A 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 haltere neuropil and sends output to the upper tectulum (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 abdominal neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult ascending neuron of the AN06A041 group with bilateral VNC arbors (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A 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). 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 AN06A060 group with bilateral VNC arbors (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A 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 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).
Adult ascending neuron of the AN06A062 group with bilateral VNC arbors (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A 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 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 ascending neuron of the AN06A080 group with bilateral VNC arbors (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A 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 tectulum 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 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 AN06A092 group with bilateral VNC arbors (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A 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 intermediate tectulum and sends output to the intermediate 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 prothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult ascending neuron of the AN06A095 group with bilateral VNC arbors (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A 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). 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 AN06A112 group with bilateral VNC arbors (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A 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 haltere neuropil and neck neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is gaba (Eckstein et al., 2024). There are approximately 6 of these cells per organism and their somas are found in the prothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult ascending neuron of the AN06B002 group with bilateral VNC arbors (Takemura et al., 2024; Marin et al., 2024). It is a primary neuron of the 06B 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 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 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 AN06B004 group with bilateral VNC arbors (Takemura et al., 2024; Marin et al., 2024). It is a primary neuron of the 06B 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 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 AN06B005 group with bilateral VNC arbors (Takemura et al., 2024; Marin et al., 2024). It is a primary neuron of the 06B 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 T3 leg neuropil and sends output to the T1 leg 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 metathoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult ascending neuron of the AN06B007 group with contralateral arbors in the VNC (Takemura et al., 2024; Marin et al., 2024). It is a primary neuron of the 06B 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). 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 mesothoracic neuromere and prothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult ascending neuron of the AN06B009 group with bilateral VNC arbors (Takemura et al., 2024; Marin et al., 2024). It is a primary neuron of the 06B 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 the brain (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 AN06B012 group with bilateral VNC arbors (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06B 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). 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 ascending neuron of the AN06B014 group with contralateral arbors in the VNC (Takemura et al., 2024; Marin et al., 2024). It is a primary neuron of the 06B 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 glutamate (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 ascending neuron of the AN06B015 group with bilateral VNC arbors (Takemura et al., 2024; Marin et al., 2024). It is a primary neuron of the 06B 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 leg neuropil and sends output to the leg neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is gaba (Eckstein et al., 2024). There are approximately 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 ascending neuron of the AN06B023 group (Takemura et al., 2024; Marin et al., 2024). It belongs to the 06B 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 (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There are approximately 4 of these cells per organism and their somas are found in the mesothoracic neuromere and prothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult ascending neuron of the AN06B026 group with bilateral VNC arbors (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06B 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 T1 leg neuropil and intermediate tectulum and sends output to the T1 leg neuropil and intermediate 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 prothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult ascending neuron of the AN06B031 group (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06B 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). 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 mesothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult ascending neuron of the AN06B034 group with bilateral VNC arbors (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06B 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). 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 ascending neuron of the AN06B037 group with bilateral VNC arbors (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06B 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 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 ascending neuron of the AN06B039 group with contralateral arbors in the VNC (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06B 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). 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 abdominal neuromere, mesothoracic neuromere, metathoracic neuromere and prothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult ascending neuron of the AN06B040 group with bilateral VNC arbors (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06B 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 median tract (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 AN06B042 group with bilateral VNC arbors (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06B 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 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 ascending neuron of the AN06B044 group with bilateral VNC arbors (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06B 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 gaba (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 AN06B045 group with bilateral VNC arbors (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06B 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 upper tectulum 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 abdominal neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult ascending neuron of the AN06B046 group with bilateral VNC arbors (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06B 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 haltere neuropil and neck neuropil and sends output to the haltere neuropil and neck neuropil (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 mesothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult ascending neuron of the AN06B048 group with bilateral VNC arbors (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06B 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 haltere neuropil and sends output to the haltere neuropil and 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 metathoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult ascending neuron of the AN06B051 group with bilateral VNC arbors (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06B 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 gaba (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 with bilateral VNC arbors (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06B 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 sends output to the brain (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 AN06B068 group with bilateral VNC arbors (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06B 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). Its predicted neurotransmitter is gaba (Eckstein et al., 2024). There are approximately 6 of these cells per organism and their somas are found in the mesothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult ascending neuron of the AN06B075 group with bilateral VNC arbors (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06B 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 sends output to the brain (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There are approximately 2 of these cells per organism and their somas are found in the prothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult efferent ascending neuron of the EA06B010 group (Takemura et al., 2024; Marin et al., 2024). It is a primary neuron of the 06B hemilineage (Takemura et al., 2024; Marin et al., 2024). It exits the VNC via the cervical connective and posterior dorsal mesothoracic nerve (Takemura et al., 2024; Marin et al., 2024). It receives input in multiple regions and sends output to multiple regions (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There are approximately 2 of these cells per organism and their somas are found in the mesothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
First born ganglion mother cell of neuroblast NB5-2.
Second born ganglion mother cell of neuroblast NB5-2.
Bilateral neuron of the HBI013 group of the adult ventral nerve cord that primarily arborizes in the haltere neuropil (Ehrhardt et al., 2023). It is an intersegmental interneuron (Ehrhardt et al., 2023). It has axonal arborization in the contralateral neck neuropil, intermediate tectulum of the mesothoracic neuromere and haltere neuropil (Ehrhardt et al., 2023). It has mixed arborization in the ipsilateral haltere neuropil (Ehrhardt et al., 2023). It has its soma in a posterior-ventral-medial position in the metathoracic neuromere (Ehrhardt et al., 2023). It belongs to the 6A hemilineage of the T3 neuromere (Ehrhardt et al., 2023). There are three of these cells per hemineuromere (Ehrhardt et al., 2023).
Bilateral neuron of the HBL001 group of the adult ventral nerve cord that primarily arborizes in the haltere neuropil (Ehrhardt et al., 2023). It is an interneuron that arborizes mainly within one neuromere of the VNC (Ehrhardt et al., 2023). It has mixed arborization in the ipsilateral haltere neuropil and the contralateral haltere neuropil (Ehrhardt et al., 2023). It has its soma in a posterior-ventral-medial position in the metathoracic neuromere (Ehrhardt et al., 2023). It belongs to the 6B hemilineage of the T3 neuromere (Ehrhardt et al., 2023). There are four of these cells per hemineuromere (Ehrhardt et al., 2023).
Any hemilineage A (Notch ON) neuron that develops from neuroblast NB5-2 during the postembryonic phase of neurogenesis.
Any hemilineage B (Notch OFF) neuron that develops from neuroblast NB5-2 during the postembryonic phase of neurogenesis.
Adult intrinsic neuron of the IN06A002 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a primary neuron of the 06A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the haltere neuropil and intermediate tectulum and sends output to the haltere neuropil and wing neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There are approximately 2 of these cells per organism and their somas are found in the mesothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN06A003 group (Takemura et al., 2024; Marin et al., 2024). It is a primary neuron of the 06A 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 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 IN06A004 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a primary neuron of the 06A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in multiple regions and sends output to the upper tectulum (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There are approximately 2 of these cells per organism and their somas are found in the prothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN06A005 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A 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 mesothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN06A006 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a primary neuron of the 06A 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 IN06A008 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a primary neuron of the 06A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the upper 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 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 IN06A009 group with bilateral arbors in a single VNC neuromere (Takemura et al., 2024; Marin et al., 2024). It is a primary neuron of the 06A 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 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 IN06A011 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A 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 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 IN06A012 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the upper tectulum 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 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 IN06A013 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the haltere neuropil and wing neuropil 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 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 IN06A014 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a primary neuron of the 06A 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 metathoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN06A016 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a primary neuron of the 06A 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 mesothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN06A018 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the haltere neuropil and intermediate tectulum and sends output to the T1 leg neuropil and intermediate 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 IN06A019 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A 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 glutamate (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 IN06A020 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A hemilineage (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 mesothoracic neuromere and metathoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN06A021 group with bilateral arbors in a single VNC neuromere (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A 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 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 IN06A022 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A 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 glutamate (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 IN06A023 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the upper tectulum 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 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 IN06A024 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A 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 IN06A025 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a primary neuron of the 06A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the abdominal neuromere and haltere neuropil and sends output to the 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 abdominal neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN06A028 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the leg neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There are approximately 6 of these cells per organism and their somas are found in the abdominal neuromere and mesothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN06A031 group with bilateral arbors in a single VNC neuromere (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the abdominal neuromere and sends output to the abdominal neuromere (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is 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 IN06A032 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A hemilineage (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There are approximately 2 of these cells per organism and their somas are found in the mesothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN06A033 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A 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 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 IN06A034 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the intermediate tectulum and neck neuropil and sends output to the intermediate tectulum and 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 intrinsic neuron of the IN06A035 group with bilateral arbors in a single VNC neuromere (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A 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 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 IN06A036 group with bilateral arbors in a single VNC neuromere (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A 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 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 IN06A037 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the upper tectulum and sends output to the haltere neuropil and wing 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 mesothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN06A038 group with bilateral arbors in a single VNC neuromere (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the haltere neuropil and sends output to the haltere neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There are approximately 2 of these cells per organism and their somas are found in the metathoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN06A039 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the upper 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 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 IN06A040 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the upper tectulum 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 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 IN06A042 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A 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 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 IN06A043 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a primary neuron of the 06A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the T3 leg neuropil and sends output to the 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 metathoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN06A044 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A 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 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 IN06A045 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A 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 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 IN06A046 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the haltere neuropil and intermediate tectulum and sends output to multiple regions (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There are approximately 2 of these cells per organism and their somas are found in the mesothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN06A047 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A hemilineage (Takemura et al., 2024; Marin et al., 2024). It sends output to the neck 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 prothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN06A048 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the upper 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 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 IN06A049 group with bilateral arbors in a single VNC neuromere (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the abdominal neuromere and sends output to the abdominal neuromere (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is 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 IN06A050 group (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the abdominal neuromere and sends output to the abdominal neuromere (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is gaba (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 IN06A051 group with bilateral arbors in a single VNC neuromere (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A 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 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 IN06A052 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the haltere neuropil and sends output to the haltere neuropil and intermediate tectulum (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is gaba (Eckstein et al., 2024). There are approximately 4 of these cells per organism and their somas are found in the abdominal neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN06A053 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A 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 haltere neuropil and intermediate tectulum (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is gaba (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 IN06A054 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A 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 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 IN06A055 group with bilateral arbors in a single VNC neuromere (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A 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 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 IN06A056 group with bilateral arbors in a single VNC neuromere (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A 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 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 IN06A057 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A 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 gaba (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 IN06A058 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the upper 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 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 IN06A059 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the intermediate tectulum and neck 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 prothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN06A061 group with bilateral arbors in a single VNC neuromere (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A 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 6 of these cells per organism and their somas are found in the metathoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN06A063 group (Takemura et al., 2024; Marin et al., 2024). It is a primary neuron of the 06A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the abdominal neuromere and sends output to the abdominal neuromere (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There are approximately 8 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 IN06A064 group with bilateral arbors in a single VNC neuromere (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the abdominal neuromere and sends output to the abdominal neuromere (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is gaba (Eckstein et al., 2024). There are approximately 6 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 IN06A065 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A 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 IN06A066 group with bilateral arbors in a single VNC neuromere (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the abdominal neuromere and sends output to the abdominal neuromere (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is gaba (Eckstein et al., 2024). There are approximately 6 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 IN06A067 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the neck 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 10 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 IN06A068 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the haltere neuropil 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 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 IN06A069 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A 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 gaba (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 IN06A070 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the haltere 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 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 IN06A071 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the haltere 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 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 IN06A072 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the tectulum and sends output to the haltere neuropil and wing neuropil (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 abdominal neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN06A073 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the haltere 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 metathoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN06A074 group with bilateral arbors in a single VNC neuromere (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A 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 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 IN06A075 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A 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 14 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 IN06A076 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A hemilineage (Takemura et al., 2024; Marin et al., 2024). It sends output to the haltere neuropil and intermediate tectulum (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is gaba (Eckstein et al., 2024). There are approximately 6 of these cells per organism and their somas are found in the prothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN06A077 group (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A 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 4 of these cells per organism and their somas are found in the metathoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN06A078 group with bilateral arbors in a single VNC neuromere (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A 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 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 IN06A079 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A 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 gaba (Eckstein et al., 2024). There are approximately 6 of these cells per organism and their somas are found in the metathoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN06A081 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A 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 gaba (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 IN06A082 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the neck 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 17 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 IN06A083 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the haltere 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 8 of these cells per organism and their somas are found in the metathoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN06A084 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A hemilineage (Takemura et al., 2024; Marin et al., 2024). It sends output to the haltere neuropil and 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 intrinsic neuron of the IN06A085 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A hemilineage (Takemura et al., 2024; Marin et al., 2024). It sends output to the haltere neuropil and tectulum (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There are approximately 4 of these cells per organism and their somas are found in the mesothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN06A086 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A 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 gaba (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 IN06A087 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in multiple regions 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 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 IN06A088 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A 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 IN06A089 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the T1 leg neuropil and neck neuropil and sends output to the haltere neuropil and 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 intrinsic neuron of the IN06A090 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the neck neuropil and sends output to the neck neuropil and tectulum (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is gaba (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 IN06A091 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the haltere neuropil 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 4 of these cells per organism and their somas are found in the abdominal neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN06A093 group with bilateral arbors in a single VNC neuromere (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A 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 4 of these cells per organism and their somas are found in the metathoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN06A094 group (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the haltere 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 9 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 IN06A096 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the haltere neuropil and intermediate tectulum (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There are approximately 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 IN06A097 group with bilateral arbors in a single VNC neuromere (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A 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 5 of these cells per organism and their somas are found in the metathoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN06A098 group with bilateral arbors in a single VNC neuromere (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the abdominal neuromere and sends output to the abdominal neuromere (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is gaba (Eckstein et al., 2024). There are approximately 4 of these cells per organism and their somas are found in the abdominal neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN06A099 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A 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 6 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 IN06A100 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A 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 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 IN06A101 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A 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 5 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 IN06A102 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the intermediate tectulum and neck neuropil (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 prothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN06A103 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A 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 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 IN06A104 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A 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 9 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 IN06A105 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the haltere neuropil and sends output to the haltere neuropil and wing 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 abdominal neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN06A106 group with bilateral arbors in a single VNC neuromere (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the abdominal neuromere and sends output to the abdominal neuromere (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is gaba (Eckstein et al., 2024). There are approximately 10 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 IN06A107 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the haltere neuropil and sends output to the haltere neuropil and wing 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 abdominal neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN06A108 group with bilateral arbors in a single VNC neuromere (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A 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 6 of these cells per organism and their somas are found in the metathoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN06A109 group with bilateral arbors in a single VNC neuromere (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the abdominal neuromere and sends output to the abdominal neuromere (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is gaba (Eckstein et al., 2024). There are approximately 6 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 IN06A110 group with bilateral arbors in a single VNC neuromere (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A 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 7 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 IN06A111 group with bilateral arbors in a single VNC neuromere (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A 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 4 of these cells per organism and their somas are found in the abdominal neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN06A113 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the neck neuropil and sends output to the haltere neuropil and neck 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 prothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN06A114 group with bilateral arbors in a single VNC neuromere (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A 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 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 IN06A115 group with bilateral arbors in a single VNC neuromere (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A 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 4 of these cells per organism and their somas are found in the metathoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN06A116 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A 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 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 IN06A117 group with bilateral arbors in a single VNC neuromere (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the abdominal neuromere and sends output to the abdominal neuromere (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is gaba (Eckstein et al., 2024). There are approximately 10 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 IN06A118 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A 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 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 IN06A119 group with bilateral arbors in a single VNC neuromere (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the abdominal neuromere and sends output to the abdominal neuromere (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is gaba (Eckstein et al., 2024). There are approximately 4 of these cells per organism and their somas are found in the abdominal neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN06A120 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A 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 6 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 IN06A121 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the neck neuropil and sends output to the haltere neuropil and 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 intrinsic neuron of the IN06A122 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the haltere neuropil and intermediate 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 mesothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN06A123 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the 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 abdominal neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN06A124 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A 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 5 of these cells per organism and their somas are found in the metathoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN06A125 group (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A 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 5 of these cells per organism and their somas are found in the metathoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN06A126 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A 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 glutamate (Eckstein et al., 2024). There are approximately 6 of these cells per organism and their somas are found in the metathoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN06A127 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A 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 IN06A128 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the haltere neuropil and sends output to the upper tectulum (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There are approximately 2 of these cells per organism and their somas are found in the metathoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN06A129 group with bilateral arbors in a single VNC neuromere (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A 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 4 of these cells per organism and their somas are found in the abdominal neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN06A130 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A 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 4 of these cells per organism and their somas are found in the abdominal neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN06A131 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in multiple regions and sends output to the haltere neuropil and wing 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 mesothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN06A132 group with bilateral arbors in a single VNC neuromere (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A 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 11 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 IN06A133 group (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A 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 4 of these cells per organism and their somas are found in the metathoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN06A134 group with bilateral arbors in a single VNC neuromere (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the abdominal neuromere and sends output to the abdominal neuromere (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is gaba (Eckstein et al., 2024). There is approximately one of these cells per organism with its soma in the abdominal neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN06A135 group (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A 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 4 of these cells per organism and their somas are found in the metathoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN06A136 group with bilateral arbors in a single VNC neuromere (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A 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 9 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 IN06A137 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A 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 glutamate (Eckstein et al., 2024). There are approximately 6 of these cells per organism and their somas are found in the metathoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN06A138 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the haltere neuropil and intermediate tectulum 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 5 of these cells per organism and their somas are found in the metathoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN06A139 group with bilateral arbors in a single VNC neuromere (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the abdominal neuromere and sends output to the abdominal neuromere (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is gaba (Eckstein et al., 2024). There is approximately one of these cells per organism with its soma in the abdominal neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN06B001 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a primary neuron of the 06B 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 IN06B003 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a primary neuron of the 06B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the T2 leg 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 mesothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN06B006 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a primary neuron of the 06B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the T1 leg neuropil and T2 leg 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 IN06B008 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06B 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 6 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 IN06B012 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06B 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 mesothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN06B013 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It belongs to the 06B hemilineage (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 mesothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN06B014 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a primary neuron of the 06B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the tectulum 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 metathoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN06B015 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a primary neuron of the 06B 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 gaba (Eckstein et al., 2024). There are approximately 4 of these cells per organism and their somas are found in the abdominal neuromere and mesothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN06B016 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06B 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 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 IN06B017 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It belongs to the 06B hemilineage (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 and metathoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN06B018 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06B 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 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 IN06B019 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in multiple regions and sends output to multiple regions (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There are approximately 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 IN06B020 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the T3 leg neuropil and sends output to the leg neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is gaba (Eckstein et al., 2024). There are approximately 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 IN06B021 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a primary neuron of the 06B 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 IN06B022 group with ipsilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the T1 leg neuropil and T2 leg neuropil and sends output to the T2 leg neuropil and T3 leg 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 mesothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN06B024 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06B 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 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 IN06B025 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06B hemilineage (Takemura et al., 2024; Marin et al., 2024). It sends output to the intermediate 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 prothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN06B027 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the T3 leg neuropil and abdominal neuromere 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 metathoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN06B028 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06B 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 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 IN06B029 group with bilateral arbors in a single VNC neuromere (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the leg neuropil and sends output to the leg neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is gaba (Eckstein et al., 2024). There are approximately 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 IN06B030 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06B 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 gaba (Eckstein et al., 2024). There are approximately 4 of these cells per organism and their somas are found in the metathoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN06B032 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06B 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 mesothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN06B033 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06B 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 gaba (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 IN06B035 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06B 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 and metathoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN06B036 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06B 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 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 IN06B038 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the haltere neuropil and wing neuropil and sends output to the haltere neuropil and wing neuropil (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 metathoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN06B040 group with contralateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the neck neuropil and sends output to the neck neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is gaba (Eckstein et al., 2024). There are approximately 5 of these cells per organism and their somas are found in the metathoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN06B042 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the 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 mesothoracic neuromere and metathoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN06B043 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06B 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 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 IN06B047 group (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06B hemilineage (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is gaba (Eckstein et al., 2024). There are approximately 16 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 IN06B049 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06B 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 metathoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN06B050 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the haltere neuropil and wing neuropil and sends output to the haltere neuropil and wing neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is gaba (Eckstein et al., 2024). There are approximately 3 of these cells per organism and their somas are found in the metathoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN06B052 group (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06B 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 6 of these cells per organism and their somas are found in the metathoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN06B053 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06B 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 gaba (Eckstein et al., 2024). There are approximately 6 of these cells per organism and their somas are found in the metathoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN06B054 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06B 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 IN06B055 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06B 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 gaba (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 IN06B056 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06B 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 gaba (Eckstein et al., 2024). There are approximately 10 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 IN06B058 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06B 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 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 IN06B059 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06B 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 15 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 IN06B060 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a primary neuron of the 06B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the T3 leg neuropil and abdominal neuromere 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 abdominal neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN06B061 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06B 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 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 IN06B062 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in multiple regions and sends output to the intermediate 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 IN06B063 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06B 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 gaba (Eckstein et al., 2024). There are approximately 9 of these cells per organism and their somas are found in the prothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN06B064 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06B 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 8 of these cells per organism and their somas are found in the mesothoracic neuromere and metathoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN06B065 group (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06B hemilineage (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There are approximately 2 of these cells per organism and their somas are found in the prothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN06B066 group (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06B 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 21 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 IN06B067 group with bilateral arbors in a single VNC neuromere (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06B hemilineage (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 IN06B069 group (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06B 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 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 IN06B070 group with contralateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the T3 leg neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is gaba (Eckstein et al., 2024). There are approximately 7 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 IN06B071 group (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06B 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 gaba (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 IN06B072 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in multiple regions and sends output to the intermediate tectulum and lower tectulum (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is gaba (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 IN06B073 group (Takemura et al., 2024; Marin et al., 2024). It is a primary neuron of the 06B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the abdominal neuromere and sends output to the abdominal neuromere (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is gaba (Eckstein et al., 2024). There are approximately 12 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 IN06B074 group with contralateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06B 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 gaba (Eckstein et al., 2024). There are approximately 10 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 IN06B076 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06B 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 gaba (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 IN06B077 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06B hemilineage (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 IN06B078 group with bilateral arbors in a single VNC neuromere (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06B 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 prothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN06B079 group (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06B 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 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 IN06B080 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06B 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 8 of these cells per organism and their somas are found in the prothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN06B081 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06B 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 gaba (Eckstein et al., 2024). There are approximately 8 of these cells per organism and their somas are found in the prothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN06B082 group (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06B 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 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 IN06B083 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06B hemilineage (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 metathoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN06B084 group with bilateral arbors in a single VNC neuromere (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06B hemilineage (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is gaba (Eckstein et al., 2024). There are approximately 3 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 IN06B085 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06B 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 IN06B086 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in multiple regions 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 prothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN06B087 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 06B 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 glutamate (Eckstein et al., 2024). There are approximately 6 of these cells per organism and their somas are found in the mesothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Any neuroblast NB5-2 (FBbt:00001376) that is part of some labial segment (FBbt:00000014).
Larval GABAergic premotor neuron (Zarin et al., 2019) that is relatively late-born in the NB5-2 Notch ON hemilineage (Mark et al., 2021). From a ventrolateral soma, it projects dorsally and arborizes in the dorsomedial neuropil (Zarin et al., 2019).
Larval GABAergic premotor neuron (Zarin et al., 2019) that is early-born in the NB5-2 Notch ON hemilineage (Mark et al., 2021). From a ventrolateral soma, it projects dorsally and arborizes in the dorsomedial neuropil (Zarin et al., 2019).
Larval interneuron that is part of the NB5-2 Notch ON hemilineage (Mark et al., 2021).
Larval interneuron of the A06i1 group that is relatively late-born in the NB5-2 Notch OFF primary hemilineage (Mark et al., 2021).
Larval interneuron of the A06i2 group that is early-born in the NB5-2 Notch OFF primary hemilineage (Mark et al., 2021).
Larval interneuron of the A06i3 group that is relatively early-born in the NB5-2 Notch OFF primary hemilineage and has predominantly ventral terminals (Mark et al., 2021).
Larval interneuron of the A06i4 group that is late-born in the NB5-2 Notch OFF primary hemilineage (Mark et al., 2021).
Larval interneuron of the A06j2 group that is relatively early-born in the NB5-2 Notch OFF primary hemilineage (Mark et al., 2021).
Larval interneuron of the A06k group that is early-born in the NB5-2 Notch OFF primary hemilineage that has predominantly ventral terminals (Mark et al., 2021).
Larval premotor neuron (Zarin et al., 2019) that is late-born in the NB5-2 Notch ON hemilineage (Mark et al., 2021). From a ventrolateral soma, it projects dorsally and arborizes in the dorsal neuropil, with ipsilateral postsynapses and contralateral presynapses (Zarin et al., 2019).
Neuromodulatory motor neuron that develops from the neuroblast 5-2 and innervates the ventral longitudinal muscle 1 (Landgraf et al., 1997). It fasciculates with the ISNb intersegmental nerve branch, innervating VL1 via type III boutons (Hoang and Chiba, 2001; Zarin et al., 2019). It soma is one segment anterior to the muscle it innervates, in the contralateral hemineuromere (Landgraf et al., 1997).
Any larval A06a neuron (FBbt:00048844) that has its soma located in some cell body rind of larval abdominal 1 neuromere (FBbt:00051990).
Any larval A06c neuron (FBbt:00048843) that has its soma located in some cell body rind of larval abdominal 1 neuromere (FBbt:00051990).
Any larval A06g1 neuron (FBbt:00051332) that has its soma located in some cell body rind of larval abdominal 1 neuromere (FBbt:00051990).
Any larval A06i1 neuron (FBbt:00051336) that has its soma located in some cell body rind of larval abdominal 1 neuromere (FBbt:00051990).
Any larval A06i2 neuron (FBbt:00051334) that has its soma located in some cell body rind of larval abdominal 1 neuromere (FBbt:00051990).
Any larval A06i3 neuron (FBbt:00048974) that has its soma located in some cell body rind of larval abdominal 1 neuromere (FBbt:00051990).
Any larval A06i4 neuron (FBbt:00051337) that has its soma located in some cell body rind of larval abdominal 1 neuromere (FBbt:00051990).
Any larval A06j2 neuron (FBbt:00051340) that has its soma located in some cell body rind of larval abdominal 1 neuromere (FBbt:00051990).
Larval A06k neuron with its cell body in the abdominal 1 neuromere. It is an ascending neuron (Winding et al., 2023).
Any larval A06x1 neuron (FBbt:00048862) that has its soma located in some cell body rind of larval abdominal 1 neuromere (FBbt:00051990).
Any larval Jaam1 neuron (FBbt:00111656) that has its soma located in some cell body rind of larval abdominal 1 neuromere (FBbt:00051990).
Any larval Jaam2 neuron (FBbt:00111657) that has its soma located in some cell body rind of larval abdominal 1 neuromere (FBbt:00051990).
Any larval Jaam3 neuron (FBbt:00111658) that has its soma located in some cell body rind of larval abdominal 1 neuromere (FBbt:00051990).
Any larval Saaghi 1 neuron (FBbt:00111659) that has its soma located in some cell body rind of larval abdominal 1 neuromere (FBbt:00051990).
Any larval Saaghi 2 neuron (FBbt:00048630) that has its soma located in some cell body rind of larval abdominal 1 neuromere (FBbt:00051990).
Any larval Saaghi 3 neuron (FBbt:00111660) that has its soma located in some cell body rind of larval abdominal 1 neuromere (FBbt:00051990).
Any larval Saaghi 4 neuron (FBbt:00048978) that has its soma located in some cell body rind of larval abdominal 1 neuromere (FBbt:00051990).
Any larval Saaghi 5 neuron (FBbt:00048979) that has its soma located in some cell body rind of larval abdominal 1 neuromere (FBbt:00051990).
Any larval Saaghi 6 neuron (FBbt:00048980) that has its soma located in some cell body rind of larval abdominal 1 neuromere (FBbt:00051990).
Any larval Saaghi 1 neuron (FBbt:00111659) that has its soma located in some cell body rind of larval abdominal 2 neuromere (FBbt:00051991).
Any larval Saaghi 3 neuron (FBbt:00111660) that has its soma located in some cell body rind of larval abdominal 2 neuromere (FBbt:00051991).
Interneuron of the larval ventral nerve cord (Heckscher et al., 2015) that is late-born in the NB5-2 Notch OFF primary hemilineage (Mark et al., 2021). The primary neurite extends into the neuropil forming one arbor that extends anteriorly and bifurcates mediolaterally (Heckscher et al., 2015). One neurite crosses the midline and forms a medial arbor that extends anteriorly, and a lateral arbor that extends both anteriorly and posteriorly; these three arbors overlap mainly with the dendrites of the A08e2 local neuron, to which it outputs (Heckscher et al., 2015). It receives input from the ipsilateral dorsal bipolar neuron (dbp) as well as substantial connections from Jaam2 and Jaam3 neurons (Heckscher et al., 2015). There is one of these neurons per hemineuromere (Heckscher et al., 2015).
Interneuron of the larval ventral nerve cord (Heckscher et al., 2015) that is relatively late-born in the NB5-2 Notch OFF primary hemilineage (Mark et al., 2021). The primary neurite extends into the neuropil forming one arbor that bifurcates and extends anteriorly and posteriorly (Heckscher et al., 2015). One neurite crosses the midline and forms an arbor that extends anteriorly in a circular manner (Heckscher et al., 2015). It receives strong input from proprioceptive multidendritic neurons and outputs onto Jaam1 (Heckscher et al., 2015). There is one of these neurons per hemineuromere (Heckscher et al., 2015).
Interneuron of the larval ventral nerve cord (Heckscher et al., 2015) that is late-born in the NB5-2 Notch OFF primary hemilineage (Mark et al., 2021). The primary neurite extends into the neuropil forming one arbor that extends anteriorly (Heckscher et al., 2015). One neurite crosses the midline and forms a broad arbor that extends anteriolaterally and overlaps with the dendrites of the A08e1 local neuron, to which it outputs (Heckscher et al., 2015). It also forms substantial synapses to Jaam1 (Heckscher et al., 2015). It receives strong input from dorsal proprioceptive multidendritic neurons and the dorsal bipolar neuron (dbp) (Heckscher et al., 2015). There is one of these neuron per hemineuromere (Heckscher et al., 2015).
Any larval Saaghi 3 neuron (FBbt:00111660) that has its soma located in some cell body rind of larval metathoracic neuromere (FBbt:00051989).
Larval primary interneuron that develops from neuroblast NB5-2 and projects contralaterally along the anterior border of the anterior commissure and immediately turns anteriorly upon reaching the contralateral connective (Bossing et al., 1996).
Larval primary interneuron that develops from neuroblast NB5-2 and projects contralaterally along the posterior border of the anterior commissure (Bossing et al., 1996).
Larval primary interneuron that develops from neuroblast NB5-2 and projects contralaterally through the posterior commissure (Bossing et al., 1996).
Larval GABAergic premotor neuron (Zarin et al., 2019) that is relatively late-born in the NB5-2 Notch ON primary hemilineage (Mark et al., 2021). Its primary neurite extends into the neuromere forming one arbor that extends anteriorly. One neurite crosses the midline and forms a terminal arbor that extends in a circular manner. It outputs to contralateral ventral and dorsal motorneurons. There is of these one neurons per hemisegment.
Larval GABAergic interneuron (Zarin et al., 2019) that is late-born in the NB5-2 Notch ON primary hemilineage (Mark et al., 2021). It has a ventrolateral soma and ipsilateral postsynapses, it crosses the midline dorsally and has contralateral presynapses (Zarin et al., 2019).
Larval premotor neuron (Zarin et al., 2019) that is relatively late-born in the NB5-2 Notch ON primary hemilineage (Mark et al., 2021). From a ventral soma, the primary neurite extends dorsally into the neuromere, with one neurite extending from it anteriorly and arborizing; another neurite extends medially and crosses the midline (Heckscher et al., 2015; Zarin et al., 2019). There is of these one neurons per hemisegment.
Larval interneuron of the Saaghi 4 group that is early-born in the NB5-2 Notch ON primary hemilineage and has predominantly dorsal terminals (Mark et al., 2021).
Larval interneuron of the Saaghi 5 group that is early-born in the NB5-2 Notch ON primary hemilineage and has predominantly dorsal terminals (Mark et al., 2021).
Larval interneuron of the Saaghi 6 group that is early-born in the NB5-2 Notch ON primary hemilineage and has predominantly dorsal terminals (Mark et al., 2021).
Motor neuron that develops from NB5-1 and innervates the ventral longitudinal muscle 1 of the segment immediately posterior to its soma (Landgraf et al., 1997). It innervates its target via type III boutons (Hoang and Chiba, 2001).
Larval V motor neuron with its soma in the abdominal 1 neuromere. It crosses the segment boundary and innervates musculature in the abdominal 2 segment. It forms type III synapses to a muscle cell of abdominal 2 ventral longitudinal muscle 1.
Larval V motor neuron with its soma in the abdominal 2 neuromere. It crosses the segment boundary and innervates musculature in the abdominal 3 segment. It forms type III synapses to a muscle cell of abdominal 3 ventral longitudinal muscle 1.
Larval V motor neuron with its soma in the abdominal 3 neuromere. It crosses the segment boundary and innervates musculature in the abdominal 4 segment. It forms type III synapses to a muscle cell of abdominal 4 ventral longitudinal muscle 1.
Larval V motor neuron with its soma in the abdominal 4 neuromere. It crosses the segment boundary and innervates musculature in the abdominal 5 segment. It forms type III synapses to a muscle cell of abdominal 5 ventral longitudinal muscle 1.
Larval V motor neuron with its soma in the abdominal 5 neuromere. It crosses the segment boundary and innervates musculature in the abdominal 6 segment. It forms type III synapses to a muscle cell of abdominal 6 ventral longitudinal muscle 1.
Larval V motor neuron with its soma in the abdominal 6 neuromere. It crosses the segment boundary and innervates musculature in the abdominal 7 segment. It forms type III synapses to a muscle cell of abdominal 7 ventral longitudinal muscle 1.
Larval V motor neuron with its soma in the metathoracic neuromere. It crosses the segment boundary and innervates musculature in the abdominal 1 segment. It forms type III synapses to a muscle cell of abdominal 1 ventral longitudinal muscle 1.
Any neuron that develops from neuroblast NB5-2 during the postembryonic phase of neurogenesis. Both hemilineages survive and are GABAergic in the adult (Lacin et al., 2019).
Any primary interneuron (FBbt:00052517) that develops from some neuroblast NB5-2 (FBbt:00001376).
Any neuroblast NB5-2 (FBbt:00001376) that is part of some maxillary segment (FBbt:00000013).
Any neuroblast NB5-2 (FBbt:00001376) that is part of some mesothoracic segment (FBbt:00000018).
Any neuroblast NB5-2 (FBbt:00001376) that is part of some metathoracic segment (FBbt:00000019).
Adult motor neuron of the MNad10 group (Takemura et al., 2024; Marin et al., 2024). It is a primary neuron of the 06A hemilineage (Takemura et al., 2024; Marin et al., 2024). It exits the VNC via the abdominal nerve (Takemura et al., 2024; Marin et al., 2024). It receives input in the abdominal neuromere and sends output to the abdomen (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There are approximately 4 of these cells per organism and their somas are found in the abdominal neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult motor neuron of the MNad19 group (Takemura et al., 2024; Marin et al., 2024). It is a primary neuron of the 06A hemilineage (Takemura et al., 2024; Marin et al., 2024). It exits the VNC via the fourth abdominal nerve (Takemura et al., 2024; Marin et al., 2024). It receives input in the abdominal neuromere and sends output to the abdomen (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is gaba (Eckstein et al., 2024). There are approximately 6 of these cells per organism and their somas are found in the abdominal neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult motor neuron of the MNhl87 group (Takemura et al., 2024; Marin et al., 2024). It is a primary neuron of the 06A hemilineage (Takemura et al., 2024; Marin et al., 2024). It exits the VNC via the metathoracic leg nerve (Takemura et al., 2024; Marin et al., 2024). It receives input in the abdominal neuromere and haltere neuropil and sends output to the metathoracic leg (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There are approximately 2 of these cells per organism and their somas are found in the metathoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Any neuron that develops from neuroblast NB5-2 at any stage of life.
Any neuron that develops from neuroblast NB5-2 during the embryonic phase of neurogenesis. The Notch ON hemilineage projects to the dorsal neuropil of both hemispheres and the Notch OFF hemilineage projects to the ventral neuropil of both hemispheres (Mark et al., 2021).
Any primary neuron that belongs to the Notch OFF hemilineage of neuroblast NB5-2 (Mark et al., 2021). These neurons tend to project to the ventral sensory neuropil of the larval ventral nerve cord (Mark et al., 2021).
Any primary neuron that belongs to the Notch OFF hemilineage of neuroblast NB5-2 (Mark et al., 2021). These neurons tend to project to the dorsal motor neuropil of the larval ventral nerve cord (Mark et al., 2021).
Bilateral neuron of the NBI003 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 contralateral neck neuropil and haltere neuropil (Ehrhardt et al., 2023). It has its soma in a posterior-ventral-medial position in the prothoracic neuromere (Ehrhardt et al., 2023). It belongs to the 6A 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 NBI004 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 contralateral neck neuropil and haltere neuropil (Ehrhardt et al., 2023). It has its soma in a posterior-ventral-medial position in the prothoracic neuromere (Ehrhardt et al., 2023). It belongs to the 6A 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 NBI005 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 contralateral neck neuropil (Ehrhardt et al., 2023). It has its soma in a posterior-ventral-medial position in the prothoracic neuromere (Ehrhardt et al., 2023). It belongs to the 6A 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 NBI006 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 contralateral neck neuropil and haltere neuropil (Ehrhardt et al., 2023). It has its soma in a posterior-ventral-medial position in the prothoracic neuromere (Ehrhardt et al., 2023). It belongs to the 6A 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 NBI007 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 contralateral neck neuropil and haltere neuropil (Ehrhardt et al., 2023). It has its soma in a posterior-ventral-lateral position in the prothoracic neuromere (Ehrhardt et al., 2023). It belongs to the 6A 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 NBI008 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 and intermediate tectulum of the prothoracic neuromere and the contralateral neck neuropil (Ehrhardt et al., 2023). It has axonal arborization in the contralateral intermediate tectulum of the mesothoracic neuromere and haltere neuropil (Ehrhardt et al., 2023). It has mixed arborization in the contralateral intermediate tectulum of the prothoracic neuromere (Ehrhardt et al., 2023). It has partitioned arborization in the contralateral wing neuropil, where dendritic and axonal arbors occupy separate regions of the neuropil (Ehrhardt et al., 2023). It has its soma in a posterior-ventral-medial position in the prothoracic neuromere (Ehrhardt et al., 2023). It belongs to the 6B 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 NBI009 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 and the contralateral neck neuropil (Ehrhardt et al., 2023). It has axonal arborization in the contralateral intermediate tectulum of the mesothoracic neuromere and haltere neuropil (Ehrhardt et al., 2023). It has its soma in a posterior-ventral-medial position in the prothoracic neuromere (Ehrhardt et al., 2023). It belongs to the 6B 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 NBI010 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 contralateral haltere neuropil (Ehrhardt et al., 2023). It has its soma in a posterior-ventral-medial position in the prothoracic neuromere (Ehrhardt et al., 2023). It belongs to the 6A 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 NBI011 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 contralateral haltere neuropil (Ehrhardt et al., 2023). It has its soma in a posterior-ventral-medial position in the prothoracic neuromere (Ehrhardt et al., 2023). It belongs to the 6A 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 NBI012 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 contralateral haltere neuropil (Ehrhardt et al., 2023). It has its soma in a posterior-ventral-lateral position in the prothoracic neuromere (Ehrhardt et al., 2023). It belongs to the 6A hemilineage of the T1 neuromere (Ehrhardt et al., 2023). There is one of these cells per hemineuromere (Ehrhardt et al., 2023).
Unilateral neuron of the NUI001 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 contralateral neck neuropil (Ehrhardt et al., 2023). It has axonal arborization in the contralateral intermediate tectulum of the mesothoracic neuromere and haltere neuropil (Ehrhardt et al., 2023). It has its soma in a posterior-ventral-medial position in the prothoracic neuromere (Ehrhardt et al., 2023). It belongs to the 6B hemilineage of the T1 neuromere (Ehrhardt et al., 2023). There are five of these cells per hemineuromere (Ehrhardt et al., 2023).
Any neuroblast NB5-2 (FBbt:00001376) that is part of some prothoracic segment (FBbt:00000017).
Any neuroblast NB5-2 (FBbt:00001376) that is part of some thoracic segment (FBbt:00000016).
Bilateral neuron of the WBI003 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 axonal arborization in the contralateral intermediate tectulum of the mesothoracic neuromere and haltere neuropil (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-ventral-medial position in the mesothoracic neuromere (Ehrhardt et al., 2023). It belongs to the 6A hemilineage of the T2 neuromere (Ehrhardt et al., 2023). There is one of these cells per hemineuromere (Ehrhardt et al., 2023).
Bilateral neuron of the WBI004 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 mixed arborization in the ipsilateral wing neuropil and intermediate tectulum of the mesothoracic neuromere (Ehrhardt et al., 2023). It has its soma in a anterior-ventral-medial position in the mesothoracic neuromere (Ehrhardt et al., 2023). It belongs to the 6A hemilineage of the T2 neuromere (Ehrhardt et al., 2023). There is one of these cells per hemineuromere (Ehrhardt et al., 2023).
Bilateral neuron of the WBI005 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 mixed arborization in the ipsilateral intermediate tectulum of the mesothoracic neuromere and the contralateral intermediate tectulum of the mesothoracic neuromere (Ehrhardt et al., 2023). It has its soma in a anterior-ventral-medial position in the mesothoracic neuromere (Ehrhardt et al., 2023). It belongs to the 6A hemilineage of the T2 neuromere (Ehrhardt et al., 2023). There is one of these cells per hemineuromere (Ehrhardt et al., 2023).
Bilateral neuron of the WBI006 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 mixed arborization in the ipsilateral wing neuropil and intermediate tectulum of the mesothoracic neuromere and the contralateral intermediate tectulum of the mesothoracic neuromere (Ehrhardt et al., 2023). It has its soma in a anterior-ventral-medial position in the mesothoracic neuromere (Ehrhardt et al., 2023). It belongs to the 6A hemilineage of the T2 neuromere (Ehrhardt et al., 2023). There is one of these cells per hemineuromere (Ehrhardt et al., 2023).
Bilateral neuron of the WBI007 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 mixed arborization in the ipsilateral wing neuropil, intermediate tectulum of the mesothoracic neuromere and haltere neuropil and the contralateral neck neuropil (Ehrhardt et al., 2023). It has its soma in a posterior-ventral-medial position in the mesothoracic neuromere (Ehrhardt et al., 2023). It belongs to the 6A hemilineage of the T2 neuromere (Ehrhardt et al., 2023). There is one of these cells per hemineuromere (Ehrhardt et al., 2023).
Bilateral neuron of the WBI008 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 contralateral wing neuropil and intermediate tectulum of the mesothoracic neuromere (Ehrhardt et al., 2023). It has mixed arborization in the ipsilateral wing neuropil (Ehrhardt et al., 2023). It has its soma in a posterior-ventral-medial position in the mesothoracic neuromere (Ehrhardt et al., 2023). It belongs to the 6A hemilineage of the T2 neuromere (Ehrhardt et al., 2023). There is one of these cells per hemineuromere (Ehrhardt et al., 2023).
Bilateral neuron of the WBI009 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 and intermediate tectulum of the mesothoracic neuromere (Ehrhardt et al., 2023). It has axonal arborization in the contralateral wing neuropil, intermediate tectulum of the mesothoracic neuromere and haltere neuropil (Ehrhardt et al., 2023). It has its soma in a anterior-ventral-medial position in the mesothoracic neuromere (Ehrhardt et al., 2023). It belongs to the 6A hemilineage of the T2 neuromere (Ehrhardt et al., 2023). There is one of these cells per hemineuromere (Ehrhardt et al., 2023).
Bilateral neuron of the WBI010 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 axonal arborization in the contralateral neck neuropil and intermediate tectulum of the mesothoracic neuromere (Ehrhardt et al., 2023). It has mixed arborization in the ipsilateral intermediate tectulum of the mesothoracic neuromere (Ehrhardt et al., 2023). It has its soma in a posterior-ventral-lateral position in the mesothoracic neuromere (Ehrhardt et al., 2023). It belongs to the 6A hemilineage of the T2 neuromere (Ehrhardt et al., 2023). There is one of these cells per hemineuromere (Ehrhardt et al., 2023).
Bilateral neuron of the WBI011 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 contralateral intermediate tectulum of the mesothoracic neuromere (Ehrhardt et al., 2023). It has mixed arborization in the contralateral wing neuropil (Ehrhardt et al., 2023). It has its soma in a posterior-ventral-lateral position in the mesothoracic neuromere (Ehrhardt et al., 2023). It belongs to the 6A hemilineage of the T2 neuromere (Ehrhardt et al., 2023). There is one of these cells per hemineuromere (Ehrhardt et al., 2023).
Bilateral neuron of the WBL012 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 and the contralateral wing neuropil and intermediate tectulum of the mesothoracic neuromere (Ehrhardt et al., 2023). It has its soma in a anterior-ventral-medial position in the mesothoracic neuromere (Ehrhardt et al., 2023). It belongs to the 6B hemilineage of the T2 neuromere (Ehrhardt et al., 2023). There is one of these cells per hemineuromere (Ehrhardt et al., 2023).
Bilateral neuron of the WBL021 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 contralateral wing neuropil (Ehrhardt et al., 2023). It has its soma in a anterior-ventral-medial position in the mesothoracic neuromere (Ehrhardt et al., 2023). It belongs to the 6B 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 WUI006 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 mixed arborization in the contralateral wing neuropil (Ehrhardt et al., 2023). It has its soma in a anterior-ventral-medial position in the mesothoracic neuromere (Ehrhardt et al., 2023). It belongs to the 6B 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 WUI007 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 mixed arborization in the contralateral wing neuropil (Ehrhardt et al., 2023). It has its soma in a posterior-ventral-medial position in the mesothoracic neuromere (Ehrhardt et al., 2023). It belongs to the 6B 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 WUI008 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 mixed arborization in the contralateral wing neuropil (Ehrhardt et al., 2023). It has its soma in a anterior-ventral-medial position in the mesothoracic neuromere (Ehrhardt et al., 2023). It belongs to the 6B 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 WUI009 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 axonal arborization in the contralateral haltere neuropil (Ehrhardt et al., 2023). It has mixed arborization in the contralateral wing neuropil (Ehrhardt et al., 2023). It has its soma in a anterior-ventral-medial position in the mesothoracic neuromere (Ehrhardt et al., 2023). It belongs to the 6B 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 WUI010 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 axonal arborization in the contralateral haltere neuropil (Ehrhardt et al., 2023). It has mixed arborization in the contralateral wing neuropil and intermediate tectulum of the mesothoracic neuromere (Ehrhardt et al., 2023). It has its soma in a anterior-ventral-medial position in the mesothoracic neuromere (Ehrhardt et al., 2023). It belongs to the 6B hemilineage of the T2 neuromere (Ehrhardt et al., 2023).
Unilateral neuron of the WUL017 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 contralateral wing neuropil (Ehrhardt et al., 2023). It has its soma in a posterior-ventral-medial position in the mesothoracic neuromere (Ehrhardt et al., 2023). It belongs to the 6B hemilineage of the T2 neuromere (Ehrhardt et al., 2023). There is one of these cells per hemineuromere (Ehrhardt et al., 2023).