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).
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.
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; Armadillo-type fold; 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.