STK25 Polyclonal Antibody, 20ul Drying & Desiccation Mutations in this gene are

Mutations in this gene are a cause of inherited human dilated cardiomyopathy with refractory congestive heart failure

Mutations in this gene are associated with ichthyosis vulgaris

branchiootic syndrome

Multiple transcript variants encoding several different isoforms have been found for ZMYND8

STK25 Polyclonal Antibody, 20ul Drying & Desiccation Mutations in this gene areThis gene encodes a member of the germinal centre kinase III (GCK III) subfamily of the sterile 20 superfamily of kinases. The encoded enzyme plays a role in serine threonine liver kinase B1 (LKB1) signaling pathway to regulate neuronal polarization and morphology of the Golgi apparatus. The protein is translocated from the Golgi apparatus to the nucleus in response to chemical anoxia and plays a role in regulation of cell death. A pseudogene