AEBP1 Polyclonal Antibody, 20ul Cell Biology Diseases associated with ZDHHC2 include

Diseases associated with ZDHHC2 include hepatocellular carcinoma and locked-in syndrome

TLR9 and TRAF6

ssential component of the eNoSC (energy-dependent nucleolar silencing) complex

Mutations in this gene are associated with the autosomal dominant disorder| encephalopathy| lethal| due to defective mitochondrial and peroxisomal fission (EMPF)

The protein encoded by this gene is a peroxisomal flavoprotein that catalyzes the oxidative deamination of D-aspartate and N-methyl D-aspartate

AEBP1 Polyclonal Antibody, 20ul Cell Biology Diseases associated with ZDHHC2 includeThis gene encodes a member of carboxypeptidase A protein family. The encoded protein may function as a transcriptional repressor and play a role in adipogenesis and smooth muscle cell differentiation. Studies in mice suggest that this gene functions in wound healing and abdominal wall development. Overexpression of this gene is associated with glioblastoma.