Table 1.
Genes identified from forward genetic screens whose loss of function causes neurodegeneration
| Gene | Defect | Protein function/human homolog | Related disease | Reference |
|---|---|---|---|---|
| drd | Phototaxis | Unknown | (70) | |
| sws | Brain histology | NTE | SPA39 | (67) |
| kdn | Bang-sensitive | Citrate synthase | (57) | |
| tko | Bang-sensitive | Mitochondrial ribosomal protein S12 | (77) | |
| bgm | Short life span | VLCFA acyl-CoA synthetase | ALD | (110) |
| Tpi | Short life span | Triosephosphate isomerase | TPI deficiency | (58) |
| Atpα | Short life span | Na+/K+ ATPase | Dystonia 12 | (127) |
| rdgB | ERG | Nir2 | (68) | |
| nmnat | ERG | Nmnat | Wallerian degeneration | (207) |