HXK I Monoclonal Antibody, 50ul[BT-MCA0759] Oligo Pool In cases of Prader-Willi syndrome

In cases of Prader-Willi syndrome

Protein FADD encoded by FADD is an adaptor molecule that interacts with various cell surface receptors and mediates cell apoptotic signals

Rho (see MIM 165390)

Gene Ontology (GO) annotations related to this gene include G-protein coupled receptor activity and transmembrane signaling receptor activity

SF3B14 encodes a 14 kDa protein subunit of the splicing factor 3b complex

HXK I Monoclonal Antibody, 50ul[BT-MCA0759] Oligo Pool In cases of Prader-Willi syndromeHexokinases phosphorylate glucose to produce glucose 6 phosphate, the first step in most glucose metabolism pathways. This gene encodes a ubiquitous form of hexokinase which localizes to the outer membrane of mitochondria. Mutations in this gene have been associated with hemolytic anemia due to hexokinase deficiency. Alternative splicing of this gene results in several transcript variants which encode different isoforms, some of which are tissue