KPCI Polyclonal Antibody, 50ul Thermo Mix Mutations in this gene have

Mutations in this gene have been associated with Kenny-Caffey syndrome (KCS) type 2 and the more severe osteocraniostenosis (OCS| also known as Gracile Bone Dysplasia)| both characterized by short stature| hypoparathyroidism| bone development abnormalities| and hypocalcemia

This gene encodes a member of the immunoglobulin superfamily

A single nucleotide variant in this gene is associated with child and adolescent obesity and shows polar overdominance

Prelamin A is farnesylated and carboxymethylated on the cysteine residue of a carboxyl-terminal CaaX motif

KPCI Polyclonal Antibody, 50ul Thermo Mix Mutations in this gene haveThis gene encodes a member of the protein kinase C (PKC) family of serine threonine protein kinases. The PKC family comprises at least eight members, which are differentially expressed and are involved in a wide variety of cellular processes. This protein kinase is calcium independent and phospholipid dependent. It is not activated by phorbolesters or diacylglycerol. This kinase can be recruited to vesicle tubular clusters (VTCs) by direct interaction