NPIP Polyclonal Antibody, 100ul Peptide Modification Mutations in this gene cause

Mutations in this gene cause Steel syndrome

PDC resides in the inner mitochondrial membrane and catalyzes the conversion of pyruvate to acetyl coenzyme A

The encoded protein acts as a homodimer and is involved in cell motility and cell-matrix interactions

GO annotations related to this gene include oxidoreductase activity andoxidoreductase activity

NPIP Polyclonal Antibody, 100ul Peptide Modification Mutations in this gene causeBelongs to the NPIP family.,Contains 1 GPS domain.,subcellular location: Colocalizes with nuclear pore complex protein NUP62.,subunit: May associate with the nuclear pore complex.,tissue specificity: Widely expressed.,