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: Chromo-like domain superfamily; Chromo domain; Post-SET domain; SET domain; Chromo/chromo shadow domain; and Chromo (CHRromatin Organisation MOdifier) 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.