| Gene ID | Entry | Entry Name | Protein Name | Type | Information | 173038 | Q9TW65 | DMD_CAEEL | Dystrophin-1 | DISRUPTION PHENOTYPE | Mutants display a phenotype of hyperactive locomotion and are hypersensitive to the acetylcholinesterase inhibitor aldicarb and are defective in maintaining neuronal positioning. Dys-1 and hlh-1 double mutants synergistically exhibit progressive myopathy. {ECO:0000269|PubMed:10369883, ECO:0000269|PubMed:10996789, ECO:0000269|PubMed:21242290, ECO:0000269|PubMed:9933302}. |
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