B23 Monoclonal Antibody, 100ul[BT-MCA0200] NGS Oligos Mutations in this gene cause

Mutations in this gene cause X-linked agammaglobulinemia type 1| which is an immunodeficiency characterized by the failure to produce mature B lymphocytes| and associated with a failure of Ig heavy chain rearrangement

The protein plays a role in the formation

which contribute to the temporal coordination of each mitotic event

Constitutive overexpression of human stanniocalcin 2 in mice resulted in pre- and postnatal growth restriction

Isoform 2 is testis specific

B23 Monoclonal Antibody, 100ul[BT-MCA0200] NGS Oligos Mutations in this gene causeThis gene encodes a phosphoprotein which moves between the nucleus and the cytoplasm. The gene product is thought to be involved in several processes including regulation of the ARF p53 pathway. A number of genes are fusion partners have been characterized, in particular the anaplastic lymphoma kinase gene on chromosome 2. Mutations in this gene are associated with acute myeloid leukemia. More than a dozen pseudogenes of this gene have been