G6PC FISH Probe

Glucose-6-phosphatase (G6Pase) is a multi-subunit integral membrane protein of the endoplasmic reticulum that is composed of a catalytic subunit and transporters for G6P, inorganic phosphate, and glucose. This gene (G6PC) is one of the three glucose-6-phosphatase catalytic-subunit-encoding genes in human: G6PC, G6PC2 and G6PC3. Glucose-6-phosphatase catalyzes the hydrolysis of D-glucose 6-phosphate to D-glucose and orthophosphate and is a key enzyme in glucose homeostasis, functioning in gluconeogenesis and glycogenolysis. Mutations in this gene cause glycogen storage disease type I (GSD1). This disease, also known as von Gierke disease, is a metabolic disorder characterized by severe hypoglycemia associated with the accumulation of glycogen and fat in the liver and kidneys.[provided by RefSeq, Feb 2011]


Gene Details
SKU Test Kits Buffer Dye Color Order Now
G6PC-20-RE 20 (40 μL) 200 μL color Request Pricing
G6PC-20-OR 20 (40 μL) 200 μL color Request Pricing
G6PC-20-GO 20 (40 μL) 200 μL color Request Pricing
G6PC-20-GR 20 (40 μL) 200 μL color Request Pricing
G6PC-20-AQ 20 (40 μL) 200 μL color Request Pricing

Gene Summary

Glucose-6-phosphatase (G6Pase) is a multi-subunit integral membrane protein of the endoplasmic reticulum that is composed of a catalytic subunit and transporters for G6P, inorganic phosphate, and glucose. This gene (G6PC) is one of the three glucose-6-phosphatase catalytic-subunit-encoding genes in human: G6PC, G6PC2 and G6PC3. Glucose-6-phosphatase catalyzes the hydrolysis of D-glucose 6-phosphate to D-glucose and orthophosphate and is a key enzyme in glucose homeostasis, functioning in gluconeogenesis and glycogenolysis. Mutations in this gene cause glycogen storage disease type I (GSD1). This disease, also known as von Gierke disease, is a metabolic disorder characterized by severe hypoglycemia associated with the accumulation of glycogen and fat in the liver and kidneys.[provided by RefSeq, Feb 2011]

Gene Details

Gene Symbol : G6PC

Gene Name : Glucose-6-phosphatase catalytic subunit

Chromosome : CHR 17: 429,007,96-429,144,32

Locus : 17q21.31

Alt. Genes : YAF2

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