Is an ortholog of C. elegans sdc-3. In C. elegans, sdc-3 is involved in several processes, including mitotic sister chromatid segregation; negative regulation of transcription by RNA polymerase II; and sex determination.
Is an ortholog of C. elegans sdc-2. In C. elegans, sdc-2 is involved in dosage compensation by hypoactivation of X chromosome and negative regulation of transcription by RNA polymerase II.
Is an ortholog of C. elegans sdc-2. In C. elegans, sdc-2 is involved in dosage compensation by hypoactivation of X chromosome and negative regulation of transcription by RNA polymerase II.
Is an ortholog of C. elegans sdc-2. In C. elegans, sdc-2 is involved in dosage compensation by hypoactivation of X chromosome and negative regulation of transcription by RNA polymerase II.
Is predicted to encode a protein with the following domains: Zinc finger C2H2 superfamily and Zinc finger C2H2-type. Is an ortholog of C. elegans sdc-1. In C. elegans, sdc-1 is involved in regulation of macromolecule metabolic process and sex determination.
Predicted to enable cysteine desulfurase activity and pyridoxal phosphate binding activity. Predicted to be involved in [2Fe-2S] cluster assembly. Is an ortholog of C. elegans nfs-1.
Predicted to enable cysteine desulfurase activity and pyridoxal phosphate binding activity. Predicted to be involved in [2Fe-2S] cluster assembly. Is an ortholog of C. elegans nfs-1.
Predicted to enable ATPase activator activity and protein-folding chaperone binding activity. Predicted to be involved in [2Fe-2S] cluster assembly and protein complex oligomerization. Is an ortholog of C. elegans dnj-15.