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G6PD gene

glucose-6-phosphate dehydrogenase

Key facts

Official symbol
G6PD
Full name
G6PD
Chromosome
X
Map location
Xq28
Organism
Homo sapiens
NCBI Gene ID
2539
Also known as
CNSHA1, G6PD1

Function summary

This gene encodes glucose-6-phosphate dehydrogenase. This protein is a cytosolic enzyme encoded by a housekeeping X-linked gene whose main function is to produce NADPH, a key electron donor in the defense against oxidizing agents and in reductive biosynthetic reactions. G6PD is remarkable for its genetic diversity. Many variants of G6PD, mostly produced from missense mutations, have been described with wide ranging levels of enzyme activity and associated clinical symptoms. G6PD deficiency may cause neonatal jaundice, acute hemolysis, or severe chronic non-spherocytic hemolytic anemia. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008].

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Data source: NCBI Gene · alsesAI Gene Library