PRMT6 Monoclonal Antibody, 100ul[BT-MCA1066] PCR Series this gene is associated with

this gene is associated with bipolar disorder and schizophrenia

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 expressed mainly in testis with weak expression in the brain

and head/neck

and cytoskeletal organization and syndecan receptors are required for internalization of the HIV-1 tat protein

PRMT6 Monoclonal Antibody, 100ul[BT-MCA1066] PCR Series this gene is associated withThe protein encoded by this gene belongs to the arginine N methyltransferase family, which catalyze the sequential transfer of methyl group from S adenosyl L methionine to the side chain nitrogens of arginine residues within proteins, to form methylated arginine derivatives and S adenosyl L homocysteine. This protein can catalyze both, the formation of omega N monomethylarginine and asymmetrical dimethylarginine, with a strong preference for the