INS Chromosome 11

Insulin
57 variants 57 Health Risk

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What This Gene Does
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. [provided by RefSeq, May 2020]
Gene Info
Gene Group
"Neuropeptides|Insulin family"
Locus Type
gene with protein product
Location
11p15.5
Ensembl
ENSG00000254647
Associated Conditions (18)
Neonatal insulin-dependent diabetes mellitus
Monogenic diabetes
Maturity-onset diabetes of the young type 10
Inborn genetic diseases
INS-related disorder
Diabetes mellitus
permanent neonatal 4
Type 1 diabetes mellitus 2
Hyperproinsulinemia
Permanent neonatal diabetes mellitus
Transient Neonatal Diabetes
Dominant/Recessive
Diabetes mellitus type 1
Type 2 diabetes mellitus
Neonatal diabetes mellitus
Amyotrophic lateral sclerosis
susceptibility to
24
Key Variants
RS1051986248
Conflicting classifications of pathogenicity
Neonatal insulin-dependent diabetes mellitus, Neonatal insulin-dependent diabetes mellitus
Health Risk
RS1057524907
Conflicting classifications of pathogenicity
Monogenic diabetes, Maturity-onset diabetes of the young type 10, Monogenic diabetes
Health Risk
RS11564720
Conflicting classifications of pathogenicity
Inborn genetic diseases, Maturity-onset diabetes of the young type 10, Inborn genetic diseases
Health Risk
RS121908259
Conflicting classifications of pathogenicity
Maturity-onset diabetes of the young type 10, INS-related disorder, Diabetes mellitus
Health Risk
RS121908260
Conflicting classifications of pathogenicity
Maturity-onset diabetes of the young type 10, Diabetes mellitus, permanent neonatal 4
Health Risk
RS121908277
Conflicting classifications of pathogenicity
Permanent neonatal diabetes mellitus, Diabetes mellitus, permanent neonatal 4
Health Risk
RS139264769
Conflicting classifications of pathogenicity
Type 1 diabetes mellitus 2, Hyperproinsulinemia, Maturity-onset diabetes of the young type 10
Health Risk
RS144093133
Conflicting classifications of pathogenicity
INS-related disorder, INS-related disorder
Health Risk
RS148685531
Conflicting classifications of pathogenicity
Hyperproinsulinemia, Hyperproinsulinemia, Hyperproinsulinemia
Health Risk
RS1554920552
Conflicting classifications of pathogenicity
Neonatal insulin-dependent diabetes mellitus, Neonatal insulin-dependent diabetes mellitus
Health Risk
RS1554920854
Conflicting classifications of pathogenicity
Neonatal insulin-dependent diabetes mellitus, Neonatal insulin-dependent diabetes mellitus
Health Risk
RS1554920985
Conflicting classifications of pathogenicity
Neonatal insulin-dependent diabetes mellitus, Neonatal insulin-dependent diabetes mellitus
Health Risk
All Variants (57)
RSID Category Clinical Significance Conditions
RS757124361 Health Risk Pathogenic/Likely pathogenic Diabetes mellitus, permanent neonatal 4, Maturity-onset diabetes of the young type 10
RS80356669 Health Risk Pathogenic/Likely pathogenic Permanent neonatal diabetes mellitus, Diabetes mellitus, permanent neonatal 4
RS886037863 Health Risk Pathogenic/Likely pathogenic Maturity-onset diabetes of the young type 10, Maturity-onset diabetes of the young type 10
RS121908261 Health Risk Pathogenic/Likely pathogenic/Likely risk allele Type 1 diabetes mellitus 2, Diabetes mellitus type 1, Monogenic diabetes
RS797045623 Health Risk Pathogenic/Likely risk allele Permanent neonatal diabetes mellitus, Neonatal insulin-dependent diabetes mellitus, Diabetes mellitus
RS80356666 Health Risk Pathogenic/Likely risk allele Permanent neonatal diabetes mellitus, Neonatal diabetes mellitus, Diabetes mellitus
RS1252051752 Health Risk Uncertain significance/Uncertain risk allele Neonatal insulin-dependent diabetes mellitus, Neonatal insulin-dependent diabetes mellitus
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