MYL3 Polyclonal Antibody, 100ul Vacuum Filter Defects in this gene cause

Defects in this gene cause X-linked Opitz-Kaveggia syndrome

and as a lymphokine that induces immunoglobulin secretion

The encoded protein contains a consensus cleavage signal found in glycosylphoshatidylinositol (GPI)-anchored proteins

also known as Sanfilippo syndrome B

also known as STAT-induced STAT inhibitor (SSI) protein family

MYL3 Polyclonal Antibody, 100ul Vacuum Filter Defects in this gene causeMYL3 encodes myosin light chain 3, an alkali light chain also referred to in the literature as both the ventricular isoform and the slow skeletal muscle isoform. Mutations in MYL3 have been identified as a cause of mid left ventricular chamber type hypertrophic cardiomyopathy.