Claudin-7(Phospho Tyr210) Polyclonal Antibody, 20ul Capsule Filter Mutations in this gene are

Mutations in this gene are associated with an autosomal dominant form of hereditary fibrosing poikiloderma (HFP)

also known as FLJ23757

|Belongs to the intercrine alpha (chemokine CxC) family

Mannose receptor C type 2 plays a role in extracellular matrix remodeling by mediating the internalization and lysosomal degradation of collagen ligands

Claudin-7(Phospho Tyr210) Polyclonal Antibody, 20ul Capsule Filter Mutations in this gene areThis gene encodes a member of the claudin family. Claudins are integral membrane proteins and components of tight junction strands. Tight junction strands serve as a physical barrier to prevent solutes and water from passing freely through the paracellular space between epithelial or endothelial cell sheets, and also play critical roles in maintaining cell polarity and signal transductions. Differential expression of this gene has been observed in