Predicted to be involved in regulation of alternative mRNA splicing, via spliceosome. Is an ortholog of C. elegans ccdc-55. In C. elegans, ccdc-55 is involved in inductive cell migration and nematode larval development.
Predicted to be involved in regulation of alternative mRNA splicing, via spliceosome. Is an ortholog of C. elegans ccdc-55. In C. elegans, ccdc-55 is involved in inductive cell migration and nematode larval development.
Predicted to be a structural constituent of ribosome. Predicted to be part of mitochondrial large ribosomal subunit. Is an ortholog of C. elegans mrpl-55.
Predicted to enable nuclear receptor 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 ZK418.10; Y47D7A.3; and unc-55.
Predicted to be involved in molybdopterin cofactor biosynthetic process. Is an ortholog of C. elegans lin-46 and moc-1. In C. elegans, lin-46 is involved in regulation of development, heterochronic.
Predicted to be involved in molybdopterin cofactor biosynthetic process. Is an ortholog of C. elegans lin-46 and moc-1. In C. elegans, lin-46 is involved in regulation of development, heterochronic.
Predicted to enable protein dimerization activity. Is an ortholog of C. elegans lin-32. In C. elegans, lin-32 is involved in several processes, including negative regulation of gliogenesis; nematode male tail tip morphogenesis; and neurogenesis.
Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. Is an ortholog of C. elegans lin-61 and mbtr-1. In C. elegans, lin-61 is involved in vulval development.