WNT7A Polyclonal Antibody, 50ul Gloves 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

and an intracellular domain consisting of multiple

being active when dephosphorylated and acts independently of CREB1 'Ser-133' phosphorylation

The family members are microtubule-dependent molecular motors that transport organelles within cells and move chromosomes during cell division

but it has been mapped to 4q

WNT7A Polyclonal Antibody, 50ul Gloves Specific mutations in DYSF haveThis gene is a member of the WNT gene family, which consists of structurally related genes that encode secreted signaling proteins. These proteins have been implicated in oncogenesis and in several developmental processes, including regulation of cell fate and patterning during embryogenesis. This gene is involved in the development of the anterior posterior axis in the female reproductive tract, and also plays a critical role in uterine smooth muscle