GAPDH Polyclonal Antibody, 50ul[BT-AP09392] Sample Library Tubes Mutations in this gene have

Mutations in this gene have been associated with autism and Asperger syndrome

and catalyzes the transfer of sulfate to position 4 of the N-acetylgalactosamine (GalNAc) residue of chondroitin and desulfated dermatan sulfate

Gene Ontology (GO) annotations related to this gene include chromatin binding and protein complex binding

subunit:May associate with the nuclear pore complex

The profile and activity of this gene product suggest that it is involved in regulating transcription and that this may be accomplished by chromatin remodeling

GAPDH Polyclonal Antibody, 50ul[BT-AP09392] Sample Library Tubes Mutations in this gene haveThis gene encodes a member of the glyceraldehyde 3 phosphate dehydrogenase protein family. The encoded protein has been identified as a moonlighting protein based on its ability to perform mechanistically distinct functions. The product of this gene catalyzes an important energy yielding step in carbohydrate metabolism, the reversible oxidative phosphorylation of glyceraldehyde 3 phosphate in the presence of inorganic phosphate and nicotinamide