TABLE 1.
Regions of the second and third chromosomes that genetically interact withhntpeb
| Stock | Deficiency (Df) or duplication (Dp) |
Cytology |
|---|---|---|
| Suppressor | ||
| Dp(2;2)Cam6 (4518) | Dp | 35B;36C |
| Df(3L)kto2 (3617) | Df | 76B1–2;76D5 |
| Df(3L)XS533 (5126) | Df | 76B4;77B |
| Moderate suppressor | ||
| Df(2L)E110 (490) | Df | 25F3–26A1;26D3–11 |
| Df(2R)H3E1 (201) | Df | 44D1–4;44F12 |
| Df(2R)stan2 (596) | Df | 46F1–2;47D1–2 |
| Df(2R)vg135 (1642) | Df | 48C–48D;49D |
| Df(2R)vg-C (754) | Df | 49A4–13;49E7–F1 |
| Dp(2;2)Cam16 (2622) | Dp | 57C4–6;60E4 |
| In(2LR)lt616-L BR27-R | Dp | 60C;60E |
| Df(2R)Px2 (2604) | Df | 60C5–6;60D9–10 |
| Df(3L)HR119 (3649) | Df | 63C2;63F7 |
| Df(3L)vin2 (2547) | Df | 67F2–3;68D6 |
| Df(3L)vin5 (2611) | Df | 68A2–3;69A1–3 |
| Df(3L)W10 (2608) | Df | 75A6–7;75C1–2 |
| Df(3L)rdgC-co2 (2052) | Df | 77A1;77D1 |
| Df(3R)D605 (823) | Df | 97E3;98A5 |
| Enhancer | ||
| Df(3R)Dl-BX12 (3012) | Df | 91F1–2;92D3–6 |
| Moderate enhancer | ||
| Dp(2;2)Cam2 (3394) | Dp | 23D1–2;26C1–2 |
| Df(2L)Dwee-delta5 (3571) | Df | 27A;28A |
| Df(2L)r10 (1491) | Df | 35D;36A6–7 |
| Df(2R)knSA3 (1150) | Df | 51B5–11;51D7–E2 |
| Df(3L)GN24 (3686) | Df | 63F6–7;64C13–15 |
| Df(3L)ZN47 (3096) | Df | 64C;65C |
| Df(3L)Delta1AK (4370) | Df | 79E5–F1;79F2–6 |
| Df(3R)Antp17 (1842) | Df | 84B1–2;84D11–12 |
| Df(3R)p712 (1968) | Df | 84D4–6;85B6 |
| Df(3R)by10 (1931) | Df | 85D8–12;85E7–F1 |
| Df(3R)DG2 (4431) | Df | 89E1–F4;91B1–B2 |
Dose-dependent modifiers of the mild rough eye phenotype observed in hntpeb adult fly eyes. The stock name is followed by the Bloomington stock number in parentheses. Each line represents either a deficiency (Df) or a duplication (Dp) that enhances or suppresses the hntpeb rough eye phenotype. The region of the chromosome that is either duplicated or absent is listed in the cytology column.