Mine Disruption Phenotype

Gene Info

  • Species: Mouse (Mus musculus)
  • GeneID: 103988
  • Symbol: Gck
  • Description: glucokinase
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Gene ID Entry Entry Name Protein Name Type Information
103988 P52792 HXK4_MOUSE Hexokinase-4 (HK4) (EC 2.7.1.1) (Glucokinase) (Hexokinase type IV) (HK IV) (Hexokinase-D) DISRUPTION PHENOTYPE Embryonic lethality caused by the absence of hexokinase activity (PubMed:7665557). Conditional deletion in pancreatic beta-cells causes severe diabetes shortly after birth leading to lethality within a week (PubMed:8530440, PubMed:9867845). Deficient islets show defective insulin secretion in response to glucose (PubMed:8530440). Conditional deletion in liver leads to mild hyperglycemia; however, mice display pronounced defects in both glycogen synthesis and glucose turnover rates during a hyperglycemic clamp (PubMed:9867845). {ECO:0000269|PubMed:7665557, ECO:0000269|PubMed:8530440, ECO:0000269|PubMed:9867845}.