IFRD2 Polyclonal Antibody, 50ul Pathway and Network Analysis Mutations in this gene cause

Mutations in this gene cause arginine:glycine amidinotransferase deficiency| an inborn error of creatine synthesis characterized by mental retardation| language impairment| and behavioral disorders

Defects in ARNTL have been linked to infertility

The encoded protein| upon tyrosine phosphorylation| has been shown to recruit the Src homology 2 domain-containing protein-tyrosine phosphatases SHP1 and SHP2

Mutations in this gene have been associated with Chronic Atrial and Intestinal Dysrhythmia (CAID) syndrome

This particular protein mediates the repulsive effect of netrin-1 and is a vascular netrin receptor

IFRD2 Polyclonal Antibody, 50ul Pathway and Network Analysis Mutations in this gene causeBelongs to the IFRD family. tissue specificity: Expressed in a variety of tissues.