PDD2L Polyclonal Antibody, 100ul Gloves Defects in this gene are

Defects in this gene are a cause of autosomal dominant centronuclear myopathy (ADCNM)

at cell-cell epithelial junctions

Dok-3 may play a significant role in the negative regulation of immunoreceptor signaling in hemopoietic cells

Two alternatively spliced transcript variants encoding different isoforms have been described for this gene

This gene encodes the d subunit of the Fo complex

PDD2L Polyclonal Antibody, 100ul Gloves Defects in this gene arePDCD2L (Programmed Cell Death 2 Like) is a Protein Coding gene. An important paralog of this gene is ENSG00000266953. Over expression suppresses AP1, CREB, NFAT, and NF kB transcriptional activation, and delays cell cycle progression at S phase.