GlyRBeta Polyclonal Antibody, 100ul Shaker&Mixing and a corresponding pseudogene has

and a corresponding pseudogene has been found on chromosome 22

The protein represents an unconventional myosin

Naturally occurring read-through transcription exists between upstream ATP5J2 (ATP synthase| H+ transporting| mitochondrial Fo complex| subunit F2) and this gene

Diseases associated with SEPT2 include gastrointestinal anthrax and acute orbital inflammation

May be involved in the regulation of p53-dependent G2 arrest of the cell cycle

GlyRBeta Polyclonal Antibody, 100ul Shaker&Mixing and a corresponding pseudogene hasGLRB encodes the beta subunit of the glycine receptor, which is a pentamer composed of alpha and beta subunits. The receptor functions as a neurotransmitter gated ion channel, which produces hyperpolarization via increased chloride conductance due to the binding of glycine to the receptor. Mutations in this gene cause startle disease, also known as hereditary hyperekplexia or congenital stiff person syndrome, a disease characterized by muscular