CCL23 Polyclonal Antibody, 20ul Low-speed Centrifuges Mutations in this gene cause

Mutations in this gene cause nephronophthisis (NPHP)| an autosomal recessive kidney disease characterized by tubular basement membrane disruption| interstitial lymphohistiocytic cell infiltration| and development of cysts at the corticomedullary border of the kidneys

This gene is found to be mutated in a type 2 diabetes family

shab-related subfamily

and other small structural RNAs

At least two isoforms of mammalian arginase exist (types I and II) which differ in their tissue distribution

CCL23 Polyclonal Antibody, 20ul Low-speed Centrifuges Mutations in this gene causeThis gene is one of several chemokine genes clustered on the q arm of chromosome 17. Chemokines form a superfamily of secreted proteins involved in immunoregulatory and inflammatory processes. The superfamily is divided into four subfamilies based on the arrangement of the N terminal cysteine residues of the mature peptide. This chemokine, a member of the CC subfamily, displays chemotactic activity on resting T lymphocytes and monocytes, lower