HSP105 Polyclonal Antibody, 50ul Vacuum Aspirator Mutations in this gene cause

Mutations in this gene cause platelet glycoprotein deficiency

A cytosolic form of this protein is encoded by a different gene and is the key enzyme of gluconeogenesis in the liver

6-hexakisphosphate (InsP6)

Among its related pathways are Sertoli-Sertoli Cell Junction Dynamics and Interleukin-3

in a region thought to be associated with susceptibility for psychiatric disorders and epilepsy

HSP105 Polyclonal Antibody, 50ul Vacuum Aspirator Mutations in this gene causeHSPH1 is a Protein Coding gene. Heat shock protein 105 kDa prevents the aggregation of denatured proteins in cells under severe stress, on which the ATP levels decrease markedly. Inhibits HSPA8 HSC70 ATPase and chaperone activities Diseases associated with HSPH1 include hepatitis d. Among its related pathways are Cellular response to heat stress and Cellular Senescence. Gene Ontology (GO) annotations related to this gene include alpha tubulin binding.