TRBeta1 Polyclonal Antibody, 20ul Cryopreservation Mutations in this gene cause

Mutations in this gene cause Charcot-Marie-Tooth disease types 1F (CMT1F) and 2E (CMT2E)

Reduced expression of this gene results in an increase in GLUT4 levels at the plasma membrane

Each of these apparently intronless genes encodes a 7-transmembrane receptor protein

Multiple pseudogenes have been reported for CEND1

TRBeta1 Polyclonal Antibody, 20ul Cryopreservation Mutations in this gene causeThe protein encoded by THRB (thyroid hormone receptor beta) is a nuclear hormone receptor for triiodothyronine. It is one of the several receptors for thyroid hormone, and has been shown to mediate the biological activities of thyroid hormone. Knockout studies in mice suggest that the different receptors, while having certain extent of redundancy, may mediate different functions of thyroid hormone. Mutations in THRB are known to be a cause of