Test ID GPI Glucose Phosphate Isomerase, Erythrocytes
Useful For
A second-order test in the evaluation of individuals with chronic hemolysis
Method Name
Kinetic Spectrophotometry (KS)
Reporting Name
Glucose Phosphate Isomerase, BSpecimen Type
Whole Blood ACD-BContainer/Tube:
Preferred: Yellow top (ACD solution B)
Acceptable: EDTA
Specimen Volume: 6 mL
Collection Instructions: Do not transfer blood to other containers.
Forms: If not ordering electronically, complete, print, and send a Benign Hematology Test Request Form (T755) with the specimen (http://www.mayomedicallaboratories.com/it-mmfiles/benign-hematology-test-request-form.pdf)
Specimen Minimum Volume
1 mL
Specimen Stability Information
Specimen Type | Temperature | Time |
---|---|---|
Whole Blood ACD-B | Refrigerated | 20 days |
Clinical Information
Erythrocyte glucose phosphate isomerase (GPI) deficiency has been reported as a cause of chronic hemolysis in numerous cases. Inheritance is autosomal recessive. Hemolytic disease of the newborn is a common presenting manifestation of GPI deficiency.
Reference Values
≥12 months: 39.3-57.7 U/g Hb
Reference values have not been established for patients who are <12 months of age.
Cautions
No significant cautionary statements
Day(s) Performed
Monday through Friday
Report Available
1 dayPerforming Laboratory

Test Classification
This test was developed and its performance characteristics determined by Mayo Clinic in a manner consistent with CLIA requirements. This test has not been cleared or approved by the U.S. Food and Drug Administration.CPT Code Information
84087