rs148660410
This variant is located in the INSR gene.
▶ClinVar annotation
Leprechaunism syndrome; Rabson-Mendenhall syndrome; Insulin-resistant diabetes mellitus AND acanthosis nigricans
View on ClinVar →About INSR
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]
View all INSR variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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