Predicted to enable DNA-binding transcription factor activity; sequence-specific DNA binding activity; and zinc ion binding activity. Predicted to be involved in regulation of DNA-templated transcription. Is an ortholog of C. elegans nhr-48.
Predicted to enable CoA pyrophosphatase activity. Is an ortholog of C. elegans ndx-8. In C. elegans, ndx-8 is involved in coenzyme A catabolic process.
Predicted to enable metallopeptidase activity. Is an ortholog of C. elegans rpn-8. In C. elegans, rpn-8 is involved in programmed cell death involved in cell development.
Predicted to be part of Golgi transport complex. Is an ortholog of C. elegans cogc-8. In C. elegans, cogc-8 is involved in gonad morphogenesis and regulation of cell migration.
Predicted to be located in membrane. Is an ortholog of C. elegans ced-8. In C. elegans, ced-8 is involved in apoptotic process; embryo development; and engulfment of apoptotic cell.
Is predicted to encode a protein with the following domains: BLOC-1-related complex subunit 8 and BLOC-1-related complex sub-unit 8. Is an ortholog of C. elegans blos-9.
Predicted to enable DNA-binding transcription factor activity; sequence-specific DNA binding activity; and zinc ion binding activity. Predicted to be involved in regulation of DNA-templated transcription. Is an ortholog of C. elegans nhr-67; nhr-64; and nhr-60.
Predicted to enable DNA-binding transcription factor activity; sequence-specific DNA binding activity; and zinc ion binding activity. Predicted to be involved in regulation of DNA-templated transcription. Is an ortholog of C. elegans nhr-67; nhr-60; and nhr-120.