Preferred Label : glucose-6-phosphate isomerase;
MeSH definition : An aldose-ketose isomerase that catalyzes the reversible interconversion of glucose
6-phosphate and fructose 6-phosphate. In prokaryotic and eukaryotic organisms it plays
an essential role in glycolytic and gluconeogenic pathways. In mammalian systems the
enzyme is found in the cytoplasm and as a secreted protein. This secreted form of
glucose-6-phosphate isomerase has been referred to as autocrine motility factor or
neuroleukin, and acts as a cytokine which binds to the AUTOCRINE MOTILITY FACTOR RECEPTOR.
Deficiency of the enzyme in humans is an autosomal recessive trait, which results
in CONGENITAL NONSPHEROCYTIC HEMOLYTIC ANEMIA.;
MeSH synonym : isomerase, glucosephosphate; phosphoglucose isomerase; isomerase, glucose 6 phosphate; isomerase, phosphohexose; phosphohexose isomerase; glucosephosphate isomerase; isomerase, glucose-6-phosphate; isomerase, phosphoglucose; glucose 6 phosphate isomerase;
MeSH hyponym : autocrine motility factor; Motility Factor, Autocrine; Tumor Autocrine Motility Factor; Tumor-Cell Autocrine Motility Factor; Tumor Cell Autocrine Motility Factor; Neuroleukin; Factor, Autocrine Motility;
MeSH CAS label : D-Glucose-6-phosphate ketol-isomerase;
MeSH Related Number : autocrine motility factor; EC 5.3.1.9;
Registry Number MeSH : EC 5.3.1.9;
Related CAS MeSH : EC 5.3.1.9 (Autocrine motility factor);
Wikipedia link : https://en.wikipedia.org/wiki/Glucose-6-phosphate isomerase;
Is substance : O;
UNII : EC 5.3.1.9;
Origin ID : D005956;
UMLS CUI : C0017759;
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An aldose-ketose isomerase that catalyzes the reversible interconversion of glucose
6-phosphate and fructose 6-phosphate. In prokaryotic and eukaryotic organisms it plays
an essential role in glycolytic and gluconeogenic pathways. In mammalian systems the
enzyme is found in the cytoplasm and as a secreted protein. This secreted form of
glucose-6-phosphate isomerase has been referred to as autocrine motility factor or
neuroleukin, and acts as a cytokine which binds to the AUTOCRINE MOTILITY FACTOR RECEPTOR.
Deficiency of the enzyme in humans is an autosomal recessive trait, which results
in CONGENITAL NONSPHEROCYTIC HEMOLYTIC ANEMIA.
http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=FR&Expert=712
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metabolism, inborn errors
rare diseases
glucose-6-phosphate isomerase
scientific and technical information
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