WFS1 Polyclonal Antibody, 100ul Custom RNA Oligos This gene encodes an intestinal

This gene encodes an intestinal serine/threonine kinase harboring a dual phosphorylation site found in mitogen-activating protein (MAP) kinases

tissue specificity:Expressed in lung and macrophages

Minichromosome maintenance complex component 5 encoded by MCM5 is structurally very similar to the CDC46 protein from S

and has been implicated in multiple inflammatory diseases

Mutations in this gene are associated with the autosomal recessive disorder Raine syndrome

WFS1 Polyclonal Antibody, 100ul Custom RNA Oligos This gene encodes an intestinalThis gene encodes a transmembrane protein, which is located primarily in the endoplasmic reticulum and ubiquitously expressed with highest levels in brain, pancreas, heart, and insulinoma beta cell lines. Mutations in this gene are associated with Wolfram syndrome, also called DIDMOAD (Diabetes Insipidus, Diabetes Mellitus, Optic Atrophy, and Deafness), an autosomal recessive disorder. The disease affects the brain and central nervous system.