Table 1 unc-7 alleles
Allele | Mutagen | Molecular lesion | Phenotype | Anti-UNC-7 staining pattern |
|---|---|---|---|---|
e5 | EMS | Q216*(CAA→TAA) | Severe | No staining |
e42 | EMS | W498*(TGG→TAG) | Severe | No staining |
e65 | EMS | A177T (GCC→ACC) | Weak | Wild-type staining |
e133 | EMS | Undetected | Moderate | Strong nr, rvg; weak vnc, dnc |
e139 | EMS | Undetected | Moderate | Strong nr, rvg; weak vnc, dnc |
hs9 | EMS | P224L (CCG→CTG) | CS | Weak signal, mostly cytoplasmic |
hs10 | EMS | C238Y (TGC→TAC) | CS | Wild-type staining |
mn382 | γ-Ray | Translocation; break point in intron 1 | Severe | Strong nr, rvg; weak vnc, dnc |
mn383 | γ-Ray | 6-kb deletion, intron 1 | Severe | Strong nr, rvg; weak vnc, dnc |
mn384 | γ-Ray | 2-kb insertion, intron 1 | Weak | Wild-type staining |
mn409 | EMS | P237L (CCA→CTA) | Severe | Weak signal, mostly cytoplasmic |