| 178150 | Q19336 | PCGF3_CAEEL | Polycomb group RING finger protein 3 homolog mig-32 (RING-domain-containing protein mig-32) | DISRUPTION PHENOTYPE | Viable, but has defects in the male-specific genital sensilla (simple sense organs) known as rays (PubMed:19211678). Defects in the migration and axon extension of the hermaphrodite specific neurons (HSN) during embryogenesis (PubMed:19211678). Ubiquitin-modified histone H2A is not detected in mutants (PubMed:19211678). RNAi-mediated knockdown in a lin-15 mutant background causes a multiple vulva (Muv) phenotype (PubMed:19211678). {ECO:0000269|PubMed:19211678}. |