Insulin R(Phospho Tyr1361) Polyclonal Antibody, 50ul Plates & Dishes Mutations in PHKA1 cause glycogen

Mutations in PHKA1 cause glycogen storage disease type 9D

it interacts with the three DNA-binding proteins of the shelterin complex

Family members are induced by various agonists such as the phorbol ester TPA and the polypeptide mitogen EGF

Naturally occurring read-through transcription exists between this gene and the neighboring downstream apolipoprotein C-II (APOC2) gene

Promotes growth and fasciculation of neurites from cultured hippocampal neurons

Insulin R(Phospho Tyr1361) Polyclonal Antibody, 50ul Plates & Dishes Mutations in PHKA1 cause glycogenThis gene 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