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. Author manuscript; available in PMC: 2021 Jan 23.
Published in final edited form as: Cell. 2020 Jan 16;180(2):373–386.e15. doi: 10.1016/j.cell.2019.12.029

Table 2.

RNAi Screen in Ventromedial (VM) PNs and ORNs: Genes, Molecular Features, Phenotypes, and Penetrances

Gene Human Ortholog Molecular Feature RNAi Phenotype % Phenotypic Penetrance (n)
CG7166 Immunoglobulin and fibronectin domains ORN trajectory error and dorsal mistargeting 74.1 (58), 38.9 (54)
CG7466/Megf8 MEGF8 Epidermal growth factor domain ORN ventral mistargeting 62.0 (50), 40.6 (64)
CG7749/kug FAT3 Cadherin repeat PN ventral mistargeting 98.0 (52), 62.0 (50)
CG17839 Immunoglobulin and fibronectin domains PN lateral mistargeting 48.1 (52), 37.5 (32)
CG33087/LRP1 LRP1 Low-density lipoprotein receptor PN and ORN local mistargeting 41.7 (48), 36.5 (52), 65.4 (52), 39.3 (28)
CG34353 LSAMP Immunoglobulin and fibronectin domains ORN posterior mistargeting 22.9 (48), 21.2 (52)
CG2054/Cht2 CHIA Chitinase ORN medial mistargeting 83.3 (54), 21.4 (42)
CG3036 Anion transporter ORN posterior mistargeting 34.0 (50), 40.3 (62)
CG3921/bark Scavenger receptor PN and ORN local mistargeting 73.1 (52), 23.9 (46)
CG4645 YIPF1 Yip domain ORN medial mistargeting 50.0 (50), 98.1 (54)*
CG6113/Lip4 LIPM Lipase PN ventral mistargeting 92.0 (50), 30.0 (30)
CG6821/Lsp1Y Hemocyanin domain Global disruption 100.0 (24), 56.0 (50)
CG8460 CHID1 Chitinase ORN dorsal mistargeting 69.6 (56)
CG9565/Nep3 ECE1 Neprilysin peptidase ORN ventral mistargeting 68.5 (54), 60.7 (56)
CG9796/GILT1 IFI30 Thiol reductase PN and ORN local mistargeting 83.3 (36), 87.0 (54)
CG14234 TMEM198 PN and ORN local mistargeting 68.9 (58), 100.0 (58)*
CG14446/dtn TMEM132E ORN dorsal mistargeting 70.4 (54), 51.9 (52)
CG31998 ORN dorsal mistargeting 70.0 (60), 50.0 (58)
CG34380/smal DDR2 Coagulation factor PN random mistargeting 39.6 (48), 26.9 (52)
CG43737 ORN dorsal and PN random mistargeting 28.9 (52), 83.3 (54)

Human orthologs were searched by the FlyBase Homologs Search tool. Only the orthologs consistently identified by four or more databases are listed. Molecular features were searched through FlyBase and UniProt. The top 6 proteins in the table belong to families of classic wiring molecules based on their structural domains; the bottom 14 proteins come from molecular families not previously linked to neural development. Phenotypic penetrance of each RNAi is listed with the number of antennal lobes examined in parentheses. Antennal lobe image of each RNAi is included in Figure S5.

*

represent two cases where pan-neuronal RNAi was lethal and PN-GAL4 was used instead to drive RNAi expression.