CD14 Monoclonal Antibody, 100ul Cellular Function Assays Alternate splice variants have been

Alternate splice variants have been described but their full length sequences have not been determined

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

This gene encodes a cytokine-like protein

Chromosomal translocations between this gene and the ret tyrosine kinase gene

translocation of part of the Y chromosome containing this gene to the X chromosome causes XX male syndrome

CD14 Monoclonal Antibody, 100ul Cellular Function Assays Alternate splice variants have beenThe 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.