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    For Research Use Only. Not For Clinical Use.


    Background

    This gene encodes insulin, a peptide hormone that plays a vital role in the regulation of carbohydrate and lipid metabolism. After removal of the precursor signal peptide, proinsulin is post-translationally cleaved into three peptides: the B chain and A chain peptides, which are covalently linked via two disulfide bonds to form insulin, and C-peptide. Binding of insulin to the insulin receptor (INSR) stimulates glucose uptake. A multitude of mutant alleles with phenotypic effects have been identified, including insulin-dependent diabetes mellitus, permanent neonatal diabetes diabetes mellitus, maturity-onset diabetes of the young type 10 and hyperproinsulinemia. There is a read-through gene, INS-IGF2, which overlaps with this gene at the 5' region and with the IGF2 gene at the 3' region.
    This insulin is obtained from pigs and is similar to human insulin. It replaces the insulin that your body would normally make. It is a short-acting insulin. It works by helping blood sugar (glucose) get into cells so your body can use it for energy.
    Related Signaling Pathways
    Insulin Signaling Pathway Insulin Signaling Pathway
    Related Diseases
    Type I Diabetes Mellitus Type I Diabetes Mellitus
    Maturity Onset Diabetes of the Young Maturity Onset Diabetes of the Young
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