INS gene in humans

E481234

The INS gene in humans is the gene that produces insulin, a key hormone that regulates blood glucose levels and is central to the development of diabetes when dysfunctional.

All labels observed (1)

Label Occurrences
INS gene in humans canonical 1

How this entity was disambiguated

Statements (51)

Predicate Object
instanceOf human gene
protein-coding gene
associatedWithDisease hyperinsulinemia
insulinoma
maturity-onset diabetes of the young
metabolic syndrome
neonatal diabetes mellitus
type 1 diabetes mellitus
type 2 diabetes mellitus
associatedWithTrait fasting plasma glucose level
insulin secretion
insulin sensitivity
biologicalProcess carbohydrate metabolism
glucose homeostasis
lipid metabolism
protein metabolism
regulation of blood glucose
encodes insulin
preproinsulin
linked to: insulin

proinsulin
expressedIn islets of Langerhans
pancreas
pancreatic beta cell
foundInSpecies Homo sapiens
hasEnsemblID ENSG00000254647
hasEntrezGeneID 3630
hasHGNCID 6081
hasPolymorphism variable number tandem repeat at 5′ region
hasStrandOrientation plus strand
hasUniProtID P01308
locatedInChromosomalBand 11p15.5
locatedOnChromosome chromosome 11
memberOfPathway MAPK signaling pathway
PI3K-Akt signaling pathway
insulin signaling pathway
molecularFunction growth factor activity
hormone activity
orthologOf mouse Ins2 gene
rat Ins1 gene
polymorphismAssociatedWith birth weight variation
type 1 diabetes risk
proteinProduct C-peptide
insulin A chain
linked to: insulin

insulin B chain
insulin precursor
regulatedBy FOXA2 transcription factor
MAFA transcription factor
NEUROD1 transcription factor
PDX1 transcription factor
glucose
transcriptProduces INS mRNA

How these facts were elicited

Referenced by (1)

Full triples — surface form annotated when it differs from this entity's canonical label.

insulin encodedBy INS gene in humans