Predicted to enable DNA binding activity. Is an ortholog of C. elegans ceh-32. In C. elegans, ceh-32 is involved in neuron differentiation and post-embryonic animal morphogenesis.
Predicted to enable GTP binding activity. Is an ortholog of C. elegans unc-59. In C. elegans, unc-59 is involved in egg-laying behavior; locomotion; and post-embryonic development.
Predicted to be involved in regulation of DNA-templated transcription. Is an ortholog of C. elegans gfl-1. In C. elegans, gfl-1 is involved in regulatory ncRNA-mediated post-transcriptional gene silencing.
Predicted to be involved in regulation of DNA-templated transcription. Is an ortholog of C. elegans gfl-1. In C. elegans, gfl-1 is involved in regulatory ncRNA-mediated post-transcriptional gene silencing.
Predicted to enable ribosome binding activity. Predicted to be involved in cytosolic ribosome assembly. Is an ortholog of C. elegans eif-6. In C. elegans, eif-6 is involved in miRNA-mediated post-transcriptional gene silencing.
Is predicted to encode a protein with the following domains: SET domain; Chromo (CHRromatin Organisation MOdifier) domain; Chromo/chromo shadow domain; Chromo domain; Chromo-like domain superfamily; and Post-SET domain. Is an ortholog of O. volvulus OVOC2197.
Predicted to be involved in chromatin organization. Predicted to be located in nucleus. Is an ortholog of C. elegans asfl-1 and unc-85. In C. elegans, unc-85 is involved in egg-laying behavior and post-embryonic development.
Predicted to enable ATP binding activity and nucleic acid binding activity. Is an ortholog of C. elegans glh-1; glh-2; and glh-3. In C. elegans, glh-1 is involved in germ cell development and post-embryonic development.