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 beta-tubulin binding activity. Predicted to be involved in post-chaperonin tubulin folding pathway and tubulin complex assembly. Is an ortholog of C. elegans tbca-1.
Predicted to enable protein tyrosine kinase activity. Is an ortholog of C. elegans sid-3. In C. elegans, sid-3 is involved in regulatory ncRNA-mediated post-transcriptional gene silencing.
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 located in membrane. Is an ortholog of C. elegans sid-1. In C. elegans, sid-1 is involved in dsRNA transport and 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 mitochondrial electron transport, NADH to ubiquinone and post-chaperonin tubulin folding pathway. Predicted to be located in mitochondrial inner membrane. Is an ortholog of C. elegans tbcc-1.
Predicted to enable ATP binding activity; DNA binding activity; and hydrolase activity. Is an ortholog of C. elegans drh-1. In C. elegans, drh-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.
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.