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

Defects in this gene are a cause of macular corneal dystrophy (MCD)

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

This gene encodes the d subunit of the Fo complex

they associate with the three catenins

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

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.