Your search for "myl2" returned 126 TaqMan® SNP Genotyping Assays
myosin light chain 2
Thus gene encodes the regulatory light chain associated with cardiac myosin beta (or slow) heavy chain. Ca+ triggers the phosphorylation of regulatory light chain that in turn triggers contraction. Mutations in this gene are associated with mid-left ventricular chamber type hypertrophic cardiomyopathy. [provided by RefSeq, Jul 2008]
Please enter the information below and press OK to send your cart to Core Services for purchase.