Aliases for IGF1 Gene
External Ids for IGF1 Gene
Previous GeneCards Identifiers for IGF1 Gene
The protein encoded by this gene is similar to insulin in function and structure and is a member of a family of proteins involved in mediating growth and development. The encoded protein is processed from a precursor, bound by a specific receptor, and secreted. Defects in this gene are a cause of insulin-like growth factor I deficiency. Alternative splicing results in multiple transcript variants encoding different isoforms that may undergo similar processing to generate mature protein. [provided by RefSeq, Sep 2015]
GeneCards Summary for IGF1 Gene
IGF1 (Insulin-Like Growth Factor 1 (Somatomedin C)) is a Protein Coding gene. Diseases associated with IGF1 include growth delay due to insulin-like growth factor type 1 deficiency and growth retardation with deafness and mental retardation due to igf1 deficiency. Among its related pathways are PI3K-Akt signaling pathway and Signaling by GPCR. GO annotations related to this gene include growth factor activity and integrin binding. An important paralog of this gene is IGF2.
UniProtKB/Swiss-Prot for IGF1 Gene
The insulin-like growth factors, isolated from plasma, are structurally and functionally related to insulin but have a much higher growth-promoting activity. May be a physiological regulator of [1-14C]-2-deoxy-D-glucose (2DG) transport and glycogen synthesis in osteoblasts. Stimulates glucose transport in rat bone-derived osteoblastic (PyMS) cells and is effective at much lower concentrations than insulin, not only regarding glycogen and DNA synthesis but also with regard to enhancing glucose uptake. May play a role in synapse maturation.
Insulin receptors (IRs) and insulin-like growth factor receptors (IGFRs) are formed from two subunits, each of which is comprised of an extracellular alpha-subunit and a transmembrane beta-subunit with intracellular tyrosine kinase activity. IR homodimers are activated by insulin.