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GENATLAS PHENOTYPE

last update : 19/09/2006

Symbol	GPX1
Location	3p21.2
Name	hemolytic anemia
Corresponding gene	GPX1
Main clinical features	hemolytic disease of the newborn with hyperbilirubinemia and Heinz bodies, associated with partial deficiency of red cell glutathione peroxidase
Genetic determination	autosomal dominant
Function/system disorder	hematology
Type	disease

Gene product

Name	glutathione peroxidase 1, cellular (GPX1)