| Gene ID | Entry | Entry Name | Protein Name | Type | Information | 181288 | G5EG78 | PXDN2_CAEEL | Peroxidasin homolog pxn-2 (EC 1.11.2.-) | DISRUPTION PHENOTYPE | RNAi-mediated knockdown causes no neuronal defects (PubMed:26194821). Furthermore RNAi-mediated knockdown rescues the neuronal defects of the pxn-1 mutant (ok785) (PubMed:26194821). {ECO:0000269|PubMed:26194821}. |
|---|