abdominal 1 neuroblast NB2-5 [FBbt_00052418]
Any neuroblast NB2-5 (FBbt:00001374) that is part of some abdominal segment 1 (FBbt:00000022).
Any neuroblast NB2-5 (FBbt:00001374) that is part of some abdominal segment 1 (FBbt:00000022).
Any neuroblast NB2-5 (FBbt:00001374) that is part of some abdominal segment (FBbt:00000021).
Adult ascending neuron of the AN17A002 group with ipsilateral VNC arbors (Takemura et al., 2024; Marin et al., 2024). It is a primary neuron of the 17A hemilineage (Takemura et al., 2024; Marin et al., 2024). It exits the VNC via the cervical connective (Takemura et al., 2024; Marin et al., 2024). Within the VNC it fasciculates with the ventral median tract of ventral cervical fasciculus (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (Eckstein et al., 2024). There are approximately 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 AN17A003 group (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 17A hemilineage (Takemura et al., 2024; Marin et al., 2024). It exits the VNC via the cervical connective (Takemura et al., 2024; Marin et al., 2024). Within the VNC it fasciculates with the ventral median tract of ventral cervical fasciculus (Takemura et al., 2024; Marin et al., 2024). It sends output to multiple regions (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (Eckstein et al., 2024). There are approximately 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 AN17A004 group with ipsilateral VNC arbors (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 17A hemilineage (Takemura et al., 2024; Marin et al., 2024). It exits the VNC via the cervical connective (Takemura et al., 2024; Marin et al., 2024). Within the VNC it fasciculates with the ventral median tract of ventral cervical fasciculus (Takemura et al., 2024; Marin et al., 2024). It receives input in multiple regions and sends output to multiple regions (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (Eckstein et al., 2024). There are approximately 2 of these cells per organism and their somas are found in the mesothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult ascending neuron of the AN17A008 group with bilateral VNC arbors (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 17A hemilineage (Takemura et al., 2024; Marin et al., 2024). It exits the VNC via the cervical connective (Takemura et al., 2024; Marin et al., 2024). Within the VNC it fasciculates with the ventral median tract of ventral cervical fasciculus (Takemura et al., 2024; Marin et al., 2024). It receives input in multiple regions and sends output to multiple regions (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (Eckstein et al., 2024). There are approximately 2 of these cells per organism and their somas are found in the metathoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult ascending neuron of the AN17A009 group with bilateral VNC arbors (Takemura et al., 2024; Marin et al., 2024). It is a primary neuron of the 17A hemilineage (Takemura et al., 2024; Marin et al., 2024). It exits the VNC via the cervical connective (Takemura et al., 2024; Marin et al., 2024). Within the VNC it fasciculates with the ventral median tract of ventral cervical fasciculus (Takemura et al., 2024; Marin et al., 2024). It sends output to multiple regions (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (Eckstein et al., 2024). There are approximately 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 AN17A012 group with bilateral VNC arbors (Takemura et al., 2024; Marin et al., 2024). It is a primary neuron of the 17A hemilineage (Takemura et al., 2024; Marin et al., 2024). It exits the VNC via the cervical connective (Takemura et al., 2024; Marin et al., 2024). Within the VNC it fasciculates with the ventral median tract of ventral cervical fasciculus (Takemura et al., 2024; Marin et al., 2024). It sends output to multiple regions (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (Eckstein et al., 2024). There are approximately 4 of these cells per organism and their somas are found in the abdominal neuromere and metathoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult ascending neuron of the AN17A013 group with bilateral VNC arbors (Takemura et al., 2024; Marin et al., 2024). It is a primary neuron of the 17A hemilineage (Takemura et al., 2024; Marin et al., 2024). It exits the VNC via the cervical connective (Takemura et al., 2024; Marin et al., 2024). Within the VNC it fasciculates with the ventral median tract of ventral cervical fasciculus (Takemura et al., 2024; Marin et al., 2024). It receives input in the leg neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (Eckstein et al., 2024). There are approximately 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 AN17A014 group (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 17A hemilineage (Takemura et al., 2024; Marin et al., 2024). It exits the VNC via the cervical connective (Takemura et al., 2024; Marin et al., 2024). Within the VNC it fasciculates with the ventral median tract of ventral cervical fasciculus (Takemura et al., 2024; Marin et al., 2024). It receives input in the leg neuropil and sends output to multiple regions (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (Eckstein et al., 2024). There are approximately 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 AN17A015 group (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 17A hemilineage (Takemura et al., 2024; Marin et al., 2024). It exits the VNC via the cervical connective (Takemura et al., 2024; Marin et al., 2024). Within the VNC it fasciculates with the ventral median tract of ventral cervical fasciculus (Takemura et al., 2024; Marin et al., 2024). It receives input in the leg neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (Eckstein et al., 2024). There are approximately 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 AN17A018 group with bilateral VNC arbors (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 17A hemilineage (Takemura et al., 2024; Marin et al., 2024). It exits the VNC via the cervical connective (Takemura et al., 2024; Marin et al., 2024). Within the VNC it fasciculates with the ventral median tract of ventral cervical fasciculus (Takemura et al., 2024; Marin et al., 2024). It sends output to multiple regions (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (Eckstein et al., 2024). There are approximately 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 AN17A024 group with bilateral VNC arbors (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 17A hemilineage (Takemura et al., 2024; Marin et al., 2024). It exits the VNC via the cervical connective (Takemura et al., 2024; Marin et al., 2024). Within the VNC it fasciculates with the ventral median tract of ventral cervical fasciculus (Takemura et al., 2024; Marin et al., 2024). It receives input in the leg neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (Eckstein et al., 2024). There are approximately 6 of these cells per organism and their somas are found in the mesothoracic neuromere, metathoracic neuromere and prothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult ascending neuron of the AN17A031 group with bilateral VNC arbors (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 17A hemilineage (Takemura et al., 2024; Marin et al., 2024). It exits the VNC via the cervical connective (Takemura et al., 2024; Marin et al., 2024). Within the VNC it fasciculates with the ventral median tract of ventral cervical fasciculus (Takemura et al., 2024; Marin et al., 2024). It receives input in multiple regions and sends output to multiple regions (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (Eckstein et al., 2024). There are approximately 2 of these cells per organism and their somas are found in the mesothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult ascending neuron of the AN17A047 group with bilateral VNC arbors (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 17A hemilineage (Takemura et al., 2024; Marin et al., 2024). It exits the VNC via the cervical connective (Takemura et al., 2024; Marin et al., 2024). Within the VNC it fasciculates with the ventral median tract of ventral cervical fasciculus (Takemura et al., 2024; Marin et al., 2024). It receives input in multiple regions and sends output to multiple regions (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (Eckstein et al., 2024). There are approximately 2 of these cells per organism and their somas are found in the prothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult ascending neuron of the AN17A050 group with bilateral VNC arbors (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 17A hemilineage (Takemura et al., 2024; Marin et al., 2024). It exits the VNC via the cervical connective (Takemura et al., 2024; Marin et al., 2024). Within the VNC it fasciculates with the ventral median tract of ventral cervical fasciculus (Takemura et al., 2024; Marin et al., 2024). It receives input in multiple regions and sends output to multiple regions (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (Eckstein et al., 2024). There are approximately 2 of these cells per organism and their somas are found in the prothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult ascending neuron of the AN17A062 group with ipsilateral VNC arbors (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 17A hemilineage (Takemura et al., 2024; Marin et al., 2024). It exits the VNC via the cervical connective (Takemura et al., 2024; Marin et al., 2024). Within the VNC it fasciculates with the ventral median tract of ventral cervical fasciculus (Takemura et al., 2024; Marin et al., 2024). It receives input in the leg neuropil and sends output to the leg neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (Eckstein et al., 2024). There are approximately 6 of these cells per organism and their somas are found in the mesothoracic neuromere, metathoracic neuromere and prothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult ascending neuron of the AN17A068 group with ipsilateral VNC arbors (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 17A hemilineage (Takemura et al., 2024; Marin et al., 2024). It exits the VNC via the cervical connective (Takemura et al., 2024; Marin et al., 2024). Within the VNC it fasciculates with the ventral median tract of ventral cervical fasciculus (Takemura et al., 2024; Marin et al., 2024). It receives input in the T3 leg neuropil and sends output to the T3 leg neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (Eckstein et al., 2024). There are approximately 2 of these cells per organism and their somas are found in the prothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult ascending neuron of the AN17A073 group (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 17A hemilineage (Takemura et al., 2024; Marin et al., 2024). It exits the VNC via the cervical connective (Takemura et al., 2024; Marin et al., 2024). Within the VNC it fasciculates with the ventral median tract of ventral cervical fasciculus (Takemura et al., 2024; Marin et al., 2024). It receives input in multiple regions and sends output to multiple regions (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (Eckstein et al., 2024). There are approximately 2 of these cells per organism and their somas are found in the mesothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult ascending neuron of the AN17A076 group with ipsilateral VNC arbors (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 17A hemilineage (Takemura et al., 2024; Marin et al., 2024). It exits the VNC via the cervical connective (Takemura et al., 2024; Marin et al., 2024). Within the VNC it fasciculates with the ventral median tract of ventral cervical fasciculus (Takemura et al., 2024; Marin et al., 2024). It receives input in the T1 leg neuropil and sends output to the T1 leg neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (Eckstein et al., 2024). There are approximately 2 of these cells per organism and their somas are found in the prothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult ascending neuron of the AN17B002 group with bilateral VNC arbors (Takemura et al., 2024; Marin et al., 2024). It is a primary neuron of the 17B hemilineage (Takemura et al., 2024; Marin et al., 2024). It exits the VNC via the cervical connective (Takemura et al., 2024; Marin et al., 2024). Within the VNC it fasciculates with the dorsal lateral tract of ventral cervical fasciculus (Takemura et al., 2024; Marin et al., 2024). It receives input in 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 abdominal neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult ascending neuron of the AN17B005 group with ipsilateral VNC arbors (Takemura et al., 2024; Marin et al., 2024). It is a primary neuron of the 17B hemilineage (Takemura et al., 2024; Marin et al., 2024). It exits the VNC via the cervical connective (Takemura et al., 2024; Marin et al., 2024). Within the VNC it fasciculates with the ventral median tract of ventral cervical fasciculus (Takemura et al., 2024; Marin et al., 2024). It receives input in multiple regions and sends output to multiple regions (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is 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 AN17B007 group with bilateral VNC arbors (Takemura et al., 2024; Marin et al., 2024). It is a primary neuron of the 17B hemilineage (Takemura et al., 2024; Marin et al., 2024). It exits the VNC via the cervical connective (Takemura et al., 2024; Marin et al., 2024). Within the VNC it fasciculates with the ventral median tract of ventral cervical fasciculus (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 AN17B008 group with bilateral VNC arbors (Takemura et al., 2024; Marin et al., 2024). It is a primary neuron of the 17B hemilineage (Takemura et al., 2024; Marin et al., 2024). It exits the VNC via the cervical connective (Takemura et al., 2024; Marin et al., 2024). Within the VNC it fasciculates with the dorsal lateral tract of ventral cervical fasciculus (Takemura et al., 2024; Marin et al., 2024). It sends output to the leg neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is gaba (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 ascending neuron of the AN17B009 group with bilateral VNC arbors (Takemura et al., 2024; Marin et al., 2024). It is a primary neuron of the 17B hemilineage (Takemura et al., 2024; Marin et al., 2024). It exits the VNC via the cervical connective (Takemura et al., 2024; Marin et al., 2024). Within the VNC it fasciculates with the dorsal lateral tract of ventral cervical fasciculus (Takemura et al., 2024; Marin et al., 2024). It sends output to multiple regions (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is 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 AN17B011 group with bilateral VNC arbors (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 17B hemilineage (Takemura et al., 2024; Marin et al., 2024). It exits the VNC via the cervical connective (Takemura et al., 2024; Marin et al., 2024). Within the VNC it fasciculates with the ventral median tract of ventral cervical fasciculus (Takemura et al., 2024; Marin et al., 2024). It receives input in multiple regions and sends output to multiple regions (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is 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 AN17B012 group with bilateral VNC arbors (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 17B hemilineage (Takemura et al., 2024; Marin et al., 2024). It exits the VNC via the cervical connective (Takemura et al., 2024; Marin et al., 2024). Within the VNC it fasciculates with the ventral median tract of ventral cervical fasciculus (Takemura et al., 2024; Marin et al., 2024). It receives input in multiple regions and sends output to multiple regions (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is 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 AN17B013 group with bilateral VNC arbors (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 17B hemilineage (Takemura et al., 2024; Marin et al., 2024). It exits the VNC via the cervical connective (Takemura et al., 2024; Marin et al., 2024). Within the VNC it fasciculates with the ventral median tract of ventral cervical fasciculus (Takemura et al., 2024; Marin et al., 2024). It receives input in multiple regions and sends output to multiple regions (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is 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 AN17B016 group with bilateral VNC arbors (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 17B hemilineage (Takemura et al., 2024; Marin et al., 2024). It exits the VNC via the cervical connective (Takemura et al., 2024; Marin et al., 2024). Within the VNC it fasciculates with the ventral median tract of ventral cervical fasciculus (Takemura et al., 2024; Marin et al., 2024). It sends output to the brain (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is 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).
Embryonic peripheral glial cell associated with the intersegmental nerve (ISN) and located laterally to ePG5. It develops from neuroblast 2-5 (von Hilchen et al., 2008) and gives rise to a perineurial glial cell (von Hilchen et al., 2013).
Embryonic peripheral glial cell associated with the intersegmental nerve (ISN) laterally to ePG7. It develops from neuroblast 2-5 (von Hilchen et al., 2008) and gives rise to a perineurial glial cell (von Hilchen et al., 2013).
First born ganglion mother cell of neuroblast NB2-5.
Unilateral neuron of the HUI001 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 dendritic arborization in the ipsilateral haltere neuropil and metathoracic leg neuropil (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 anterior-dorsal-medial position in the metathoracic neuromere (Ehrhardt et al., 2023). It belongs to the 17A hemilineage of the T3 neuromere (Ehrhardt et al., 2023). There is one of these cells per hemineuromere (Ehrhardt et al., 2023).
Unilateral neuron of the HUI002 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 dendritic arborization in the ipsilateral haltere neuropil and metathoracic leg neuropil (Ehrhardt et al., 2023). It has axonal arborization in the ipsilateral wing neuropil (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 anterior-dorsal-medial position in the metathoracic neuromere (Ehrhardt et al., 2023). It belongs to the 17A hemilineage of the T3 neuromere (Ehrhardt et al., 2023). There is one of these cells per hemineuromere (Ehrhardt et al., 2023).
Unilateral neuron of the HUI003 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 dendritic arborization in the ipsilateral haltere neuropil and metathoracic leg neuropil (Ehrhardt et al., 2023). It has axonal arborization in the ipsilateral wing neuropil (Ehrhardt et al., 2023). It has partitioned arborization in the ipsilateral intermediate tectulum of the mesothoracic neuromere, where dendritic and axonal arbors occupy separate regions of the neuropil (Ehrhardt et al., 2023). It has its soma in a anterior-dorsal-medial position in the metathoracic neuromere (Ehrhardt et al., 2023). It belongs to the 17A hemilineage of the T3 neuromere (Ehrhardt et al., 2023).
Unilateral neuron of the HUI004 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 dendritic arborization in the ipsilateral haltere neuropil and metathoracic leg neuropil (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 anterior-dorsal-medial position in the metathoracic neuromere (Ehrhardt et al., 2023). It belongs to the 17A hemilineage of the T3 neuromere (Ehrhardt et al., 2023). There is one of these cells per hemineuromere (Ehrhardt et al., 2023).
Unilateral neuron of the HUI005 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 dendritic arborization in the ipsilateral metathoracic leg neuropil (Ehrhardt et al., 2023). It has axonal arborization in the ipsilateral wing neuropil (Ehrhardt et al., 2023). It has partitioned arborization in the ipsilateral haltere neuropil, where dendritic and axonal arbors occupy separate regions of the neuropil (Ehrhardt et al., 2023). It has its soma in a anterior-dorsal-medial position in the metathoracic neuromere (Ehrhardt et al., 2023). It belongs to the 17A hemilineage of the T3 neuromere (Ehrhardt et al., 2023). There is one of these cells per hemineuromere (Ehrhardt et al., 2023).
Adult intrinsic neuron of the IN17A001 group with ipsilateral arbors in a single VNC neuromere (Takemura et al., 2024; Marin et al., 2024). It is a primary neuron of the 17A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the leg neuropil and sends output to the leg neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (Eckstein et al., 2024). There are approximately 6 of these cells per organism and their somas are found in the mesothoracic neuromere, metathoracic neuromere and prothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN17A007 group (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 17A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the leg neuropil and sends output to the leg neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (Eckstein et al., 2024). There are approximately 6 of these cells per organism and their somas are found in the mesothoracic neuromere, metathoracic neuromere and prothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN17A011 group with ipsilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a primary neuron of the 17A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the T3 leg neuropil and haltere neuropil and sends output to multiple regions (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (Eckstein et al., 2024). There are approximately 2 of these cells per organism and their somas are found in the metathoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN17A013 group with ipsilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a primary neuron of the 17A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the T3 leg neuropil and sends output to the T3 leg neuropil and lower tectulum (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (Eckstein et al., 2024). There are approximately 2 of these cells per organism and their somas are found in the metathoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN17A016 group with bilateral arbors in a single VNC neuromere (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 17A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the leg neuropil and sends output to the leg neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (Eckstein et al., 2024). There are approximately 6 of these cells per organism and their somas are found in the mesothoracic neuromere, metathoracic neuromere and prothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN17A017 group with ipsilateral arbors in a single VNC neuromere (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 17A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the leg neuropil and sends output to the leg neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (Eckstein et al., 2024). There are approximately 6 of these cells per organism and their somas are found in the mesothoracic neuromere, metathoracic neuromere and prothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN17A019 group (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 17A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the leg neuropil and sends output to the leg neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (Eckstein et al., 2024). There are approximately 6 of these cells per organism and their somas are found in the mesothoracic neuromere, metathoracic neuromere and prothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN17A020 group (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 17A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the leg neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (Eckstein et al., 2024). There are approximately 6 of these cells per organism and their somas are found in the mesothoracic neuromere, metathoracic neuromere and prothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN17A022 group with ipsilateral arbors in a single VNC neuromere (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 17A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the leg neuropil and sends output to the leg neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (Eckstein et al., 2024). There are approximately 6 of these cells per organism and their somas are found in the mesothoracic neuromere, metathoracic neuromere and prothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN17A023 group with ipsilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 17A hemilineage (Takemura et al., 2024; Marin et al., 2024). It sends output to multiple regions (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (Eckstein et al., 2024). There are approximately 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 IN17A025 group with ipsilateral arbors in a single VNC neuromere (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 17A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the leg neuropil and sends output to the leg neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (Eckstein et al., 2024). There are approximately 6 of these cells per organism and their somas are found in the mesothoracic neuromere, metathoracic neuromere and prothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN17A027 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 17A 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 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 IN17A028 group with ipsilateral arbors in a single VNC neuromere (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 17A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the leg neuropil and sends output to the leg neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (Eckstein et al., 2024). There are approximately 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 IN17A029 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 17A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in multiple regions (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (Eckstein et al., 2024). There are approximately 2 of these cells per organism and their somas are found in the mesothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN17A030 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 17A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in multiple regions and sends output to multiple regions (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (Eckstein et al., 2024). There are approximately 2 of these cells per organism and their somas are found in the mesothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN17A032 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 17A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in multiple regions and sends output to multiple regions (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (Eckstein et al., 2024). There are approximately 2 of these cells per organism and their somas are found in the mesothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN17A033 group with ipsilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 17A 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 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 IN17A034 group with ipsilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 17A 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 is approximately one of these cells per organism with its soma in the mesothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN17A035 group with ipsilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 17A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in multiple regions and sends output to multiple regions (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (Eckstein et al., 2024). There are approximately 2 of these cells per organism and their somas are found in the mesothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN17A037 group with ipsilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 17A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in multiple regions and sends output to multiple regions (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (Eckstein et al., 2024). There are approximately 4 of these cells per organism and their somas are found in the metathoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN17A039 group with ipsilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 17A 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 3 of these cells per organism and their somas are found in the mesothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN17A040 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 17A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in multiple regions and sends output to multiple regions (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (Eckstein et al., 2024). There are approximately 2 of these cells per organism and their somas are found in the mesothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN17A041 group with ipsilateral arbors in a single VNC neuromere (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 17A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the leg neuropil and sends output to the leg neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There are approximately 6 of these cells per organism and their somas are found in the mesothoracic neuromere, metathoracic neuromere and prothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN17A042 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 17A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in multiple regions and sends output to multiple regions (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (Eckstein et al., 2024). There are approximately 2 of these cells per organism and their somas are found in the mesothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN17A043 group with ipsilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 17A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the T3 leg neuropil and sends output to the T3 leg neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (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 IN17A044 group with ipsilateral arbors in a single VNC neuromere (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 17A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the leg neuropil and sends output to the leg neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (Eckstein et al., 2024). There are approximately 6 of these cells per organism and their somas are found in the mesothoracic neuromere, metathoracic neuromere and prothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN17A045 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 17A hemilineage (Takemura et al., 2024; Marin et al., 2024). It sends output to the tectulum and wing neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (Eckstein et al., 2024). There are approximately 2 of these cells per organism and their somas are found in the mesothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN17A046 group with ipsilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 17A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the T3 leg neuropil and sends output to the T3 leg neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (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 IN17A048 group with ipsilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 17A 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 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 IN17A049 group with ipsilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 17A hemilineage (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 IN17A051 group with ipsilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 17A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in multiple regions and sends output to multiple regions (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (Eckstein et al., 2024). There are approximately 2 of these cells per organism and their somas are found in the metathoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN17A052 group with ipsilateral arbors in a single VNC neuromere (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 17A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the leg neuropil and sends output to the leg neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (Eckstein et al., 2024). There are approximately 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 IN17A053 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 17A hemilineage (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (Eckstein et al., 2024). There are approximately 4 of these cells per organism and their somas are found in the metathoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN17A055 group with ipsilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 17A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the wing neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (Eckstein et al., 2024). There are approximately 2 of these cells per organism and their somas are found in the mesothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN17A056 group with ipsilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 17A hemilineage (Takemura et al., 2024; Marin et al., 2024). It sends output to multiple regions (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (Eckstein et al., 2024). There are approximately 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 IN17A057 group with ipsilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 17A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the intermediate tectulum and wing neuropil and sends output to multiple regions (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (Eckstein et al., 2024). There are approximately 2 of these cells per organism and their somas are found in the mesothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN17A058 group with ipsilateral arbors in a single VNC neuromere (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 17A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the leg neuropil and sends output to the leg neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (Eckstein et al., 2024). There are approximately 4 of these cells per organism and their somas are found in the mesothoracic neuromere and metathoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN17A059 group with ipsilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 17A hemilineage (Takemura et al., 2024; Marin et al., 2024). It sends output to multiple regions (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (Eckstein et al., 2024). There are approximately 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 IN17A060 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 17A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the tectulum and sends output to the haltere neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There are approximately 4 of these cells per organism and their somas are found in the mesothoracic neuromere and metathoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN17A061 group with ipsilateral arbors in a single VNC neuromere (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 17A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the leg neuropil and sends output to the leg neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (Eckstein et al., 2024). There are approximately 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 IN17A063 group with ipsilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 17A hemilineage (Takemura et al., 2024; Marin et al., 2024). It sends output to multiple regions (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (Eckstein et al., 2024). There are approximately 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 IN17A064 group with ipsilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 17A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in multiple regions and sends output to the wing neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There are approximately 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 IN17A065 group with ipsilateral arbors in a single VNC neuromere (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 17A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the T1 leg neuropil and sends output to the T1 leg neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (Eckstein et al., 2024). There are approximately 2 of these cells per organism and their somas are found in the prothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN17A066 group with ipsilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 17A hemilineage (Takemura et al., 2024; Marin et al., 2024). It sends output to the leg neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (Eckstein et al., 2024). There are approximately 2 of these cells per organism and their somas are found in the metathoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN17A067 group with ipsilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 17A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in multiple regions (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (Eckstein et al., 2024). There are approximately 2 of these cells per organism and their somas are found in the mesothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN17A069 group with ipsilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 17A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the wing neuropil and sends output to the intermediate tectulum and wing neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There are approximately 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 IN17A071 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 17A 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 acetylcholine (Eckstein et al., 2024). There are approximately 2 of these cells per organism and their somas are found in the mesothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN17A072 group with ipsilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 17A 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 acetylcholine (Eckstein et al., 2024). There are approximately 3 of these cells per organism and their somas are found in the mesothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN17A074 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 17A 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 acetylcholine (Eckstein et al., 2024). There are approximately 2 of these cells per organism and their somas are found in the metathoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN17A075 group with ipsilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 17A 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 acetylcholine (Eckstein et al., 2024). There are approximately 2 of these cells per organism and their somas are found in the mesothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN17A077 group with ipsilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 17A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the wing neuropil and sends output to the upper tectulum (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (Eckstein et al., 2024). There are approximately 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 IN17A078 group with ipsilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 17A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in multiple regions and sends output to the wing neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (Eckstein et al., 2024). There are approximately 4 of these cells per organism and their somas are found in the mesothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN17A079 group with ipsilateral arbors in a single VNC neuromere (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 17A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the leg neuropil and sends output to the leg neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (Eckstein et al., 2024). There are approximately 4 of these cells per organism and their somas are found in the mesothoracic neuromere and prothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN17A080 group with ipsilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 17A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in multiple regions and sends output to multiple regions (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (Eckstein et al., 2024). There are approximately 2 of these cells per organism and their somas are found in the mesothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN17A081 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 17A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the wing neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (Eckstein et al., 2024). There are approximately 2 of these cells per organism and their somas are found in the mesothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN17A082 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 17A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the T3 leg 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 acetylcholine (Eckstein et al., 2024). There are approximately 2 of these cells per organism and their somas are found in the metathoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN17A083 group with ipsilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 17A hemilineage (Takemura et al., 2024; Marin et al., 2024). It sends output to multiple regions (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (Eckstein et al., 2024). There are approximately 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 IN17A084 group with ipsilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 17A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the wing neuropil and sends output to the lower tectulum and wing neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (Eckstein et al., 2024). There are approximately 3 of these cells per organism and their somas are found in the mesothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN17A085 group with ipsilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 17A 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 acetylcholine (Eckstein et al., 2024). There are approximately 3 of these cells per organism and their somas are found in the mesothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN17A086 group with ipsilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 17A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the T3 leg neuropil and wing neuropil and sends output to the wing neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (Eckstein et al., 2024). There are approximately 2 of these cells per organism and their somas are found in the metathoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN17A087 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 17A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in multiple regions and sends output to multiple regions (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (Eckstein et al., 2024). There are approximately 2 of these cells per organism and their somas are found in the mesothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN17A088 group with ipsilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 17A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in multiple regions and sends output to multiple regions (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (Eckstein et al., 2024). There are approximately 2 of these cells per organism and their somas are found in the mesothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN17A089 group with ipsilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 17A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in multiple regions and sends output to multiple regions (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (Eckstein et al., 2024). There are approximately 2 of these cells per organism and their somas are found in the mesothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN17A090 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 17A hemilineage (Takemura et al., 2024; Marin et al., 2024). It sends output to multiple regions (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (Eckstein et al., 2024). There are approximately 3 of these cells per organism and their somas are found in the mesothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN17A091 group with ipsilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 17A 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 haltere neuropil and wing neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (Eckstein et al., 2024). There are approximately 2 of these cells per organism and their somas are found in the metathoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN17A092 group with ipsilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 17A 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 acetylcholine (Eckstein et al., 2024). There are approximately 2 of these cells per organism and their somas are found in the metathoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN17A093 group with ipsilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 17A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the wing neuropil and sends output to multiple regions (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (Eckstein et al., 2024). There are approximately 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 IN17A094 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 17A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in multiple regions and sends output to multiple regions (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (Eckstein et al., 2024). There are approximately 4 of these cells per organism and their somas are found in the mesothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN17A095 group with ipsilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 17A hemilineage (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (Eckstein et al., 2024). There are approximately 2 of these cells per organism and their somas are found in the mesothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN17A096 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 17A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in multiple regions and sends output to multiple regions (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (Eckstein et al., 2024). There are approximately 2 of these cells per organism and their somas are found in the mesothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN17A097 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 17A 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 acetylcholine (Eckstein et al., 2024). There are approximately 3 of these cells per organism and their somas are found in the mesothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN17A098 group with ipsilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 17A 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 intermediate tectulum and wing neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (Eckstein et al., 2024). There are approximately 2 of these cells per organism and their somas are found in the metathoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN17A099 group with ipsilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 17A 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 acetylcholine (Eckstein et al., 2024). There are approximately 3 of these cells per organism and their somas are found in the mesothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN17A100 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 17A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the wing neuropil and sends output to the haltere neuropil and wing neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (Eckstein et al., 2024). There are approximately 2 of these cells per organism and their somas are found in the mesothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN17A101 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 17A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in multiple regions and sends output to multiple regions (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (Eckstein et al., 2024). There are approximately 2 of these cells per organism and their somas are found in the mesothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN17A102 group with ipsilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 17A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in multiple regions and sends output to the wing neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (Eckstein et al., 2024). There are approximately 2 of these cells per organism and their somas are found in the metathoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN17A103 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 17A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in multiple regions and sends output to the wing neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (Eckstein et al., 2024). There are approximately 2 of these cells per organism and their somas are found in the metathoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN17A104 group with ipsilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 17A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the T3 leg 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 acetylcholine (Eckstein et al., 2024). There are approximately 2 of these cells per organism and their somas are found in the metathoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN17A105 group with ipsilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 17A 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 intermediate tectulum and wing neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There are approximately 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 IN17A106 group with ipsilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 17A hemilineage (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (Eckstein et al., 2024). There are approximately 4 of these cells per organism and their somas are found in the mesothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN17A107 group with ipsilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 17A hemilineage (Takemura et al., 2024; Marin et al., 2024). It sends output to multiple regions (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (Eckstein et al., 2024). There are approximately 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 IN17A108 group with ipsilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 17A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in multiple regions and sends output to the intermediate tectulum and wing neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (Eckstein et al., 2024). There are approximately 2 of these cells per organism and their somas are found in the metathoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN17A109 group with ipsilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 17A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in multiple regions and sends output to the T2 leg neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (Eckstein et al., 2024). There are approximately 2 of these cells per organism and their somas are found in the mesothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN17A110 group with ipsilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 17A 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 intermediate tectulum and wing neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is glutamate (Eckstein et al., 2024). There are approximately 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 IN17A111 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 17A 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 acetylcholine (Eckstein et al., 2024). There are approximately 5 of these cells per organism and their somas are found in the mesothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN17A113 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 17A hemilineage (Takemura et al., 2024; Marin et al., 2024). It sends output to the tectulum (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (Eckstein et al., 2024). There are approximately 4 of these cells per organism and their somas are found in the mesothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN17A114 group with ipsilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 17A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in multiple regions and sends output to multiple regions (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (Eckstein et al., 2024). There are approximately 2 of these cells per organism and their somas are found in the mesothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN17A115 group with ipsilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 17A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the T3 leg neuropil and sends output to the intermediate tectulum and wing neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (Eckstein et al., 2024). There are approximately 2 of these cells per organism and their somas are found in the metathoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN17A116 group with ipsilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 17A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in multiple regions and sends output to multiple regions (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (Eckstein et al., 2024). There are approximately 2 of these cells per organism and their somas are found in the mesothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN17A117 group with ipsilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 17A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in multiple regions (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (Eckstein et al., 2024). There are approximately 2 of these cells per organism and their somas are found in the mesothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN17A118 group with ipsilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 17A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in multiple regions and sends output to the T2 leg neuropil (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (Eckstein et al., 2024). There are approximately 3 of these cells per organism and their somas are found in the mesothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN17A119 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 17A hemilineage (Takemura et al., 2024; Marin et al., 2024). It sends output to the tectulum (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (Eckstein et al., 2024). There are approximately 4 of these cells per organism and their somas are found in the mesothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN17A120 group with ipsilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 17A hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in multiple regions (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is acetylcholine (Eckstein et al., 2024). There are approximately 2 of these cells per organism and their somas are found in the mesothoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN17B001 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a primary neuron of the 17B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in the upper tectulum (Takemura et al., 2024; Marin et al., 2024). Its predicted neurotransmitter is gaba (Eckstein et al., 2024). There are approximately 2 of these cells per organism and their somas are found in the abdominal neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN17B003 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a primary neuron of the 17B 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 abdominal neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN17B004 group with ipsilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a primary neuron of the 17B 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 metathoracic neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN17B006 group with ipsilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a primary neuron of the 17B 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 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 IN17B008 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a primary neuron of the 17B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in multiple regions 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 IN17B010 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 17B hemilineage (Takemura et al., 2024; Marin et al., 2024). It receives input in multiple regions 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 abdominal neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN17B014 group with bilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 17B 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 abdominal neuromere (Takemura et al., 2024; Marin et al., 2024).
Adult intrinsic neuron of the IN17B015 group with ipsilateral arbors in multiple VNC neuromeres (Takemura et al., 2024; Marin et al., 2024). It is a secondary neuron of the 17B 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 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).
Any neuroblast NB2-5 (FBbt:00001374) that is part of some labial segment (FBbt:00000014).
Larval primary interneuron that develops from neuroblast NB2-5 projects contralaterally across the anterior commissure (Schmidt et al., 1997).
Larval NB2-5 contralateral primary interneuron that has a more medially shifted soma and a longer anteriorly-extending contralateral projection compared to other contralateral NB2-5 interneurons (Schmidt et al., 1997).
Larval primary interneuron that develops from neuroblast NB2-5 and projects ipsilaterally (Schmidt et al., 1997).
Any neuron that develops from neuroblast NB2-5 during the postembryonic phase of neurogenesis. These are all Notch ON hemilineage neurons, as the Notch OFF hemilineage is eliminated by apoptosis (Lacin et al., 2019). In the adult, these neurons are cholinergic (Lacin et al., 2019).
Any primary interneuron (FBbt:00052517) that develops from some neuroblast NB2-5 (FBbt:00001374).
Any primary motor neuron (FBbt:00052518) that develops from some neuroblast NB2-5 (FBbt:00001374).
Any neuroblast NB2-5 (FBbt:00001374) that is part of some mandibular segment (FBbt:00000012).
Any neuroblast NB2-5 (FBbt:00001374) that is part of some maxillary segment (FBbt:00000013).
Any neuron that develops from neuroblast NB2-5 at any stage of life.
Any neuron that develops from neuroblast NB2-5 during the embryonic phase of neurogenesis.
Any neuroblast NB2-5 (FBbt:00001374) that is part of some thoracic segment (FBbt:00000016).
Bilateral neuron of the WBI013 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 wing neuropil (Ehrhardt et al., 2023). It has its soma in a anterior-dorsal-lateral position in the mesothoracic neuromere (Ehrhardt et al., 2023). It belongs to the 17A 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 WBL013 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 accessory mesothoracic neuropil and wing neuropil and the contralateral wing neuropil (Ehrhardt et al., 2023). It has its soma in a anterior-dorsal-lateral position in the mesothoracic neuromere (Ehrhardt et al., 2023). It belongs to the 17A hemilineage of the T2 neuromere (Ehrhardt et al., 2023).
Bilateral neuron of the WBL014 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 dendritic arborization in the ipsilateral accessory mesothoracic neuropil (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 (Ehrhardt et al., 2023). It has its soma in a anterior-dorsal-lateral position in the mesothoracic neuromere (Ehrhardt et al., 2023). It belongs to the 17A 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 WBL015 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 dendritic arborization in the contralateral intermediate tectulum of the mesothoracic neuromere (Ehrhardt et al., 2023). It has mixed arborization in the ipsilateral wing neuropil and the contralateral wing neuropil (Ehrhardt et al., 2023). It has partitioned arborization in the ipsilateral intermediate tectulum of the mesothoracic neuromere, where dendritic and axonal arbors occupy separate regions of the neuropil (Ehrhardt et al., 2023). It has its soma in a anterior-dorsal-lateral position in the mesothoracic neuromere (Ehrhardt et al., 2023). It belongs to the 17A 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 WBL016 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 dendritic arborization in the contralateral intermediate tectulum of the mesothoracic neuromere (Ehrhardt et al., 2023). It has mixed arborization in the ipsilateral wing neuropil and the contralateral wing neuropil (Ehrhardt et al., 2023). It has partitioned arborization in the ipsilateral intermediate tectulum of the mesothoracic neuromere, where dendritic and axonal arbors occupy separate regions of the neuropil (Ehrhardt et al., 2023). It has its soma in a anterior-dorsal-lateral position in the mesothoracic neuromere (Ehrhardt et al., 2023). It belongs to the 17A 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 WBL017 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 dendritic arborization in the contralateral intermediate tectulum of the mesothoracic neuromere (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 (Ehrhardt et al., 2023). It has its soma in a anterior-dorsal-lateral position in the mesothoracic neuromere (Ehrhardt et al., 2023). It belongs to the 17A 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 WBL018 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 dendritic arborization in the contralateral intermediate tectulum of the mesothoracic neuromere (Ehrhardt et al., 2023). It has partitioned arborization in the ipsilateral wing neuropil and intermediate tectulum of the mesothoracic neuromere and 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 anterior-dorsal-lateral position in the mesothoracic neuromere (Ehrhardt et al., 2023). It belongs to the 17A 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 WBL019 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 dendritic arborization in the contralateral intermediate tectulum of the mesothoracic neuromere (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 (Ehrhardt et al., 2023). It has its soma in a anterior-dorsal-lateral position in the mesothoracic neuromere (Ehrhardt et al., 2023). It belongs to the 17A 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 WBL020 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 and intermediate tectulum of the mesothoracic neuromere (Ehrhardt et al., 2023). It has partitioned arborization in the ipsilateral wing neuropil and intermediate tectulum of the mesothoracic neuromere, where dendritic and axonal arbors occupy separate regions of the neuropil (Ehrhardt et al., 2023). It has its soma in a anterior-dorsal-lateral position in the mesothoracic neuromere (Ehrhardt et al., 2023). It belongs to the 17A 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 WUL007 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 dendritic arborization in the ipsilateral accessory mesothoracic neuropil (Ehrhardt et al., 2023). It has mixed arborization in the ipsilateral wing neuropil (Ehrhardt et al., 2023). It has its soma in a anterior-dorsal-lateral position in the mesothoracic neuromere (Ehrhardt et al., 2023). It belongs to the 17A 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 WUL008 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 accessory mesothoracic neuropil and wing neuropil (Ehrhardt et al., 2023). It has its soma in a anterior-dorsal-lateral position in the mesothoracic neuromere (Ehrhardt et al., 2023). It belongs to the 17A 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 WUL009 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 accessory mesothoracic neuropil and wing neuropil (Ehrhardt et al., 2023). It has its soma in a anterior-dorsal-lateral position in the mesothoracic neuromere (Ehrhardt et al., 2023). It belongs to the 17A 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 WUL010 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 accessory mesothoracic neuropil and wing neuropil (Ehrhardt et al., 2023). It has its soma in a anterior-dorsal-lateral position in the mesothoracic neuromere (Ehrhardt et al., 2023). It belongs to the 17A 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 WUL011 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 accessory mesothoracic neuropil and wing neuropil (Ehrhardt et al., 2023). It has its soma in a anterior-dorsal-lateral position in the mesothoracic neuromere (Ehrhardt et al., 2023). It belongs to the 17A 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 WUL012 group of the adult ventral nerve cord that primarily arborizes in the wing neuropil (Ehrhardt et al., 2023). It is an interneuron that arborizes mainly within one neuromere of the VNC (Ehrhardt et al., 2023). It has mixed arborization in the ipsilateral wing neuropil and intermediate tectulum of the mesothoracic neuromere (Ehrhardt et al., 2023). It has its soma in a anterior-dorsal-lateral position in the mesothoracic neuromere (Ehrhardt et al., 2023). It belongs to the 17A hemilineage of the T2 neuromere (Ehrhardt et al., 2023). There is one of these cells per hemineuromere (Ehrhardt et al., 2023).