TTR mouse Monoclonal Antibody(10D8), 50ul Organelle Studies This gene encodes a member

This gene encodes a member of the latrophilin subfamily of G-protein coupled receptors (GPCR)

Mutations in this gene are associated with Meckel syndrome type 8

and its protein signaling is likely a molecular switch that governs adipogenesis

and syndromic craniosynostosis

The metabotropic glutamate receptors are a family of G protein-coupled receptors

TTR mouse Monoclonal Antibody(10D8), 50ul Organelle Studies This gene encodes a memberThis gene encodes transthyretin, one of the three prealbumins including alpha 1 antitrypsin, transthyretin and orosomucoid. Transthyretin is a carrier protein it transports thyroid hormones in the plasma and cerebrospinal fluid, and also transports retinol (vitamin A) in the plasma. The protein consists of a tetramer of identical subunits. More than 80 different mutations in this gene have been reported most mutations are related to amyloid