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INSR gene

insulin receptor

Key facts

Official symbol
INSR
Full name
INSR
Chromosome
19
Map location
19p13.2
Organism
Homo sapiens
NCBI Gene ID
3643
Also known as
CD220, HHF5

Function summary

This 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 the inherited severe insulin resistance syndromes including type A insulin resistance syndrome, Donohue syndrome and Rabson-Mendenhall syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2015].

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Data source: NCBI Gene · alsesAI Gene Library