GSK3Beta mouse Monoclonal Antibody(2C6), 50ul Filtration Mutations in this gene can

Mutations in this gene can also cause congenital hypothyroidism non-goitrous type 5

and belongs to the steroid 5-alpha reductase family

This gene encodes a member of the WNT1 inducible signaling pathway (WISP) protein subfamily

A processed non-transcribed pseudogene located in an intron of a sodium transporter gene on chromosome 5 has been defined for this gene

An important paralog of this gene is GLB1L2

GSK3Beta mouse Monoclonal Antibody(2C6), 50ul Filtration Mutations in this gene canThe protein encoded by this gene is a serine threonine kinase, belonging to the glycogen synthase kinase subfamily. It is involved in energy metabolism, neuronal cell development, and body pattern formation. Polymorphisms in this gene have been implicated in modifying risk of Parkinson disease, and studies in mice show that overexpression of this gene may be relevant to the pathogenesis of Alzheimer disease. Alternatively spliced transcript variants