CD14 Monoclonal Antibody, 100ul Cellular Function Assays Specific mutations in DYSF have

Specific mutations in DYSF have been shown to cause autosomal recessive limb girdle muscular dystrophy type 2B (LGMD2B) as well as Miyoshi myopathy

type I receptors phosphorylate cytoplasmic SMAD transcription factors

This gene encodes a cytokine-like protein

Chromosomal translocations between this gene and the ret tyrosine kinase gene

Polymorphisms of this gene may be associated with hunger

CD14 Monoclonal Antibody, 100ul Cellular Function Assays Specific mutations in DYSF haveThe protein encoded by this gene is a surface antigen that is preferentially expressed on monocytes macrophages. It cooperates with other proteins to mediate the innate immune response to bacterial lipopolysaccharide. Alternative splicing results in multiple transcript variants encoding the same protein.