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 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 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 be located in membrane. Is an ortholog of C. elegans sid-1; chup-1; and C08A9.3. In C. elegans, sid-1 is involved in dsRNA transport and 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.
Predicted to be involved in regulatory ncRNA-mediated gene silencing. Predicted to be part of RISC complex. Is an ortholog of C. elegans tsn-1. In C. elegans, tsn-1 is involved in miRNA-mediated post-transcriptional gene silencing.