Predicted to be involved in Golgi organization. Located in endoplasmic reticulum. Human ortholog(s) of this gene implicated in Smith-McCort dysplasia 1. Is an ortholog of human DYM (dymeclin).
Predicted to enable several functions, including ATP binding activity; helicase activity; and nucleic acid binding activity. Predicted to be located in cytoplasm. Is an ortholog of human DDX60 (DExD/H-box helicase 60) and DDX60L (DExD/H-box 60 like).
Predicted to enable box H/ACA snoRNA binding activity. Predicted to be involved in snoRNA guided rRNA pseudouridine synthesis. Predicted to be located in nucleolus. Predicted to be part of box H/ACA snoRNP complex. Is an ortholog of human GAR1 (GAR1 ribonucleoprotein).
Is affected by clk-1 and etr-1 based on microarray and RNA-seq studies. Is predicted to encode a protein with the following domains: Serpentine type 7TM GPCR chemoreceptor Srh; 7TM GPCR, serpentine receptor class h (Srh); and Nematode receptor-like serpentine class H.
Is predicted to encode a protein with the following domains: Dyggve-Melchior-Clausen syndrome protein and Dymeclin. Is an ortholog of C. elegans C47D12.2.
Is predicted to encode a protein with the following domains: Dyggve-Melchior-Clausen syndrome protein and Dymeclin. Is an ortholog of C. elegans C47D12.2.
Is predicted to encode a protein with the following domains: Dyggve-Melchior-Clausen syndrome protein and Dymeclin. Is an ortholog of C. elegans C47D12.2.
Is predicted to encode a protein with the following domains: Dyggve-Melchior-Clausen syndrome protein and Dymeclin. Is an ortholog of C. elegans C47D12.2.