INSR Chromosome 19

Insulin receptor
110 variants 110 Health Risk

Upload your DNA to see your personal genotypes for variants in INSR.

What This Gene Does
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]
Gene Info
Gene Group
"CD molecules|Fibronectin type III domain containing|Insulin receptor family"
Locus Type
gene with protein product
Location
19p13.2
Ensembl
ENSG00000171105
Associated Conditions (16)
Leprechaunism syndrome
Insulin-resistant diabetes mellitus AND acanthosis nigricans
Rabson-Mendenhall syndrome
Hyperinsulinism due to INSR deficiency
Clear cell carcinoma of kidney
Inborn genetic diseases
INSR-related disorder
Nonpapillary renal cell carcinoma
Monogenic diabetes
Type 2 diabetes mellitus
Bailey-Bloch congenital myopathy
Insulin resistance
Gastric cancer
46
XY disorder of sex development
Insulin-resistant diabetes mellitus
Key Variants
RS111502197
Conflicting classifications of pathogenicity
Leprechaunism syndrome, Insulin-resistant diabetes mellitus AND acanthosis nigricans, Rabson-Mendenhall syndrome
Health Risk
RS111993466
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS121913136
Conflicting classifications of pathogenicity
Leprechaunism syndrome, INSR-related disorder, Leprechaunism syndrome
Health Risk
RS121913147
Conflicting classifications of pathogenicity
Insulin-resistant diabetes mellitus AND acanthosis nigricans, Rabson-Mendenhall syndrome, Leprechaunism syndrome
Health Risk
RS13306449
Conflicting classifications of pathogenicity
Leprechaunism syndrome, Insulin-resistant diabetes mellitus AND acanthosis nigricans, Rabson-Mendenhall syndrome
Health Risk
RS1347473020
Conflicting classifications of pathogenicity
INSR-related disorder, INSR-related disorder
Health Risk
RS138528064
Conflicting classifications of pathogenicity
INSR-related disorder, INSR-related disorder
Health Risk
RS140573575
Conflicting classifications of pathogenicity
Health Risk
RS140852238
Conflicting classifications of pathogenicity
Insulin-resistant diabetes mellitus AND acanthosis nigricans, Insulin-resistant diabetes mellitus AND acanthosis nigricans
Health Risk
RS142391704
Conflicting classifications of pathogenicity
Insulin-resistant diabetes mellitus AND acanthosis nigricans, Rabson-Mendenhall syndrome, Leprechaunism syndrome
Health Risk
RS142654992
Conflicting classifications of pathogenicity
Insulin-resistant diabetes mellitus AND acanthosis nigricans, Leprechaunism syndrome, Rabson-Mendenhall syndrome
Health Risk
RS142910337
Conflicting classifications of pathogenicity
Monogenic diabetes, INSR-related disorder, Monogenic diabetes
Health Risk
All Variants (110)
RSID Category Clinical Significance Conditions
RS267607184 Health Risk Pathogenic Leprechaunism syndrome, Leprechaunism syndrome
RS387906538 Health Risk Pathogenic Leprechaunism syndrome, Leprechaunism syndrome
RS52836744 Health Risk Pathogenic Leprechaunism syndrome, Leprechaunism syndrome
RS587776819 Health Risk Pathogenic Rabson-Mendenhall syndrome, Rabson-Mendenhall syndrome
RS587776820 Health Risk Pathogenic Rabson-Mendenhall syndrome, Rabson-Mendenhall syndrome
RS778989302 Health Risk Pathogenic
RS797045624 Health Risk Pathogenic Hyperinsulinism due to INSR deficiency, Hyperinsulinism due to INSR deficiency
RS886037750 Health Risk Pathogenic Rabson-Mendenhall syndrome, Rabson-Mendenhall syndrome
RS369102740 Health Risk Uncertain significance/Uncertain risk allele Leprechaunism syndrome, Rabson-Mendenhall syndrome, Insulin-resistant diabetes mellitus AND acanthosis nigricans
RS777565396 Health Risk Uncertain significance/Uncertain risk allele Leprechaunism syndrome, Rabson-Mendenhall syndrome, Insulin-resistant diabetes mellitus AND acanthosis nigricans
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