rs193922285
This is a variant in the GCK gene that changes a methionine to an isoleucine.
▶ClinVar annotation
Hyperinsulinism due to glucokinase deficiency (HHF3); Maturity onset diabetes mellitus in young (MODY); Maturity-onset diabetes of the young type 2; Monogenic diabetes; Permanent neonatal diabetes mellitus (PNDM); Permanent neonatal diabetes mellitus 1; Transient Neonatal Diabetes, Recessive; Type 2 diabetes mellitus; not specified
View on ClinVar →About GCK
This gene encodes a member of the hexokinase family of proteins. Hexokinases phosphorylate glucose to produce glucose-6-phosphate, the first step in most glucose metabolism pathways. In contrast to other forms of hexokinase, this enzyme is not inhibited by its product glucose-6-phosphate but remains active while glucose is abundant. The use of multiple promoters and alternative splicing of this gene result in distinct protein isoforms that exhibit tissue-specific expression in the pancreas and liver. In the pancreas, this enzyme plays a role in glucose-stimulated insulin secretion, while in the liver, this enzyme is important in glucose uptake and conversion to glycogen. Mutations in this gene that alter enzyme activity have been associated with multiple types of diabetes and hyperinsulinemic hypoglycemia. [provided by RefSeq, Aug 2017]
View all GCK variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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