GCN2(Phospho Thr899) Polyclonal Antibody, 100ul Immune Repertoire Sequencing 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

and in three-color analyses with ZsYellow and HcRed

The encoded protein however is a pseudoreceptor

It was identified by its similarity to leukocyte-associated immunoglobulin-like receptor 1

GCN2(Phospho Thr899) Polyclonal Antibody, 100ul Immune Repertoire Sequencing Mutations in this gene causeThis gene encodes a member of a family of kinases that phosphorylate the alpha subunit of eukaryotic translation initiation factor 2 (EIF2), resulting in the downregulaton of protein synthesis. The encoded protein responds to amino acid deprivation by binding uncharged transfer RNAs. It may also be activated by glucose deprivation and viral infection. Mutations in this gene have been found in individuals suffering from autosomal recessive pulmonary