MYL6B Polyclonal Antibody, 100ul DNA/RNA Isolation & Purification Mutations in this gene are

Mutations in this gene are associated with lipoid proteinosis disorder (also known as hyalinosis cutis et mucosae or Urbach-Wiethe disease) that is characterized by generalized thickening of skin

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is located approximately 25 kb away from CYP1A1 on chromosome 15

Defects in this gene are also associated with Senior-Loken syndrome type 1

miscellaneous:The EU sequence has the INV (3) allotypic marker| Ala-45 and Val-83

MYL6B Polyclonal Antibody, 100ul DNA/RNA Isolation & Purification Mutations in this gene areMyosin is a hexameric ATPase cellular motor protein. It is composed of two heavy chains, two nonphosphorylatable alkali light chains, and two phosphorylatable regulatory light chains. This gene encodes a myosin alkali light chain expressed in both slow twitch skeletal muscle and in nonmuscle tissue. Alternative splicing results in multiple transcript variants.