MARK1/2/3/4 Polyclonal Antibody, 50ul[BT-AP05227] Endonucleases & Exonucleases This autosomal dominant disorder is

This autosomal dominant disorder is characterized by abnormal water reabsorption by kidney tubules due

PABPC4 or IPABP (inducible PABP) was isolated as an activation-induced T-cell mRNA encoding a protein

and inactive

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

MARK1/2/3/4 Polyclonal Antibody, 50ul[BT-AP05227] Endonucleases & Exonucleases This autosomal dominant disorder isMARK1 is a Protein Coding gene. Serine threonine protein kinase MARK1 involved in cell polarity and microtubule dynamics regulation. Phosphorylates DCX, MAP2, MAP4 and MAPT TAU. Involved in cell polarity by phosphorylating the microtubule associated proteins MAP2, MAP4 and MAPT TAU at KXGS motifs, causing detachment from microtubules, and their disassembly. Involved in the regulation of neuronal migration through its dual activities in regulating