Insulin R Polyclonal Antibody, 50ul[BT-AP04563] Site-directed Mutagenesis Mutations of this gene are

Mutations of this gene are associated with Seckel syndrome

Dysregulated production of IL6 and this receptor are implicated in the pathogenesis of many diseases

which is adjacent to this gene on chromosome 19

GPR176is a Protein Coding gene

which functions in the regulation of transcription by bridging interactions between gene-specific regulatory factors

Insulin R Polyclonal Antibody, 50ul[BT-AP04563] Site-directed Mutagenesis Mutations of this gene areINSR encodes a member of the receptor tyrosine kinase family of proteins. The encoded preproprotein is proteolytically processed to generate alpha and beta subunits that form a heterotetrameric receptor. Binding of insulin or other ligands to this receptor activates the insulin signaling pathway, which regulates glucose uptake and release, as well as the synthesis and storage of carbohydrates, lipids and protein. Mutations in this gene underlie the