NOL11 Polyclonal Antibody, 100ul Culture Plate Inserts Most WFDC gene members are

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

Mutation in this gene causes dimethylglycine dehydrogenase deficiency

This gene encodes a nuclear protein that contains a p53 binding domain at the N-terminus and a RING finger domain at the C-terminus

as well as other neuronal ceroid-lipofuscinosis (CLN) genes

NOL11 Polyclonal Antibody, 100ul Culture Plate Inserts Most WFDC gene members areNOL11 (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.