NOL11 Polyclonal Antibody, 100ul Culture Plate Inserts Mutation in this gene causes

Mutation in this gene causes dimethylglycine dehydrogenase deficiency

interacts with other molecules implicated in homeostasis

This gene plays a role in membrane trafficking between the trans-Golgi network and endosomes

Most WFDC gene members are localized to chromosome 20q12-q13 in two clusters: centromeric and telomeric

and also functions in lymphocyte costimulatory signaling

NOL11 Polyclonal Antibody, 100ul Culture Plate Inserts Mutation in this gene causesNOL11 (Nucleolar Protein 11) is a Protein Coding gene. Among its related pathways are rRNA processing in the nucleus and cytosol and Gene Expression. Ribosome biogenesis factor. May be required for both optimal rDNA transcription and small subunit (SSU) pre rRNA processing at sites A, A0, 1 and 2b.