SRPK2 Polyclonal Antibody, 20ul Gene Synthesis Several transcript variants encoding different

Several transcript variants encoding different isoforms| have been identified for this gene

Mutations resulting in haploinsufficiency for this gene cause familial acne inversa-2 (ACNINV2)

The 5' portion of this gene and two neighboring cytochrome p450 genes are included in a deletion that results in an autosomal-dominant form of nonsyndromic optic nerve aplasia (ONA)

Many variants of G6PD

SRPK2 Polyclonal Antibody, 20ul Gene Synthesis Several transcript variants encoding differentCatalytic activity: ATP + a protein = ADP + a phosphoprotein.,cofactor: Magnesium.,enzyme regulation: Activated by phosphorylation on Ser 52 and Ser 588.,Phosphorylates RS domain containing proteins, such as SFRS1 and SFRS2 on serine residues. Role in spliceosome assembly and in mediating the trafficking of splicing factors. Appears to mediate HBV core protein phosphorylation which is a prerequisite for pregenomic RNA encapsidation into viral