Test Code PKLRZ PKLR Full Gene Analysis, Varies
Ordering Guidance
Preliminary screening tests, such as complete blood cell count with peripheral smear, direct Coombs test, and pyruvate kinase enzyme activity assays (preferably as a part of EEEV1 / Red Blood Cell [RBC] Enzyme Evaluation, Blood) should be performed before ordering this test.
Targeted testing (also called site-specific or known variants testing) is available for variants identified in the PKLR gene. See FMTT / Familial Variant, Targeted Testing, Varies. To obtain more information about this testing option, call 800-533-1710.
Necessary Information
1. PKLR Gene Sequencing Patient Information is required. Testing may proceed without the patient information; however, it aids in providing a more thorough interpretation. Ordering healthcare professionals are strongly encouraged to complete the form and send it with the specimen.
2. Include healthcare professional's name and phone number with specimen.
Specimen Required
Specimen Type: Whole blood
Patient Preparation: A previous bone marrow transplant from an allogenic donor will interfere with testing. For instructions for testing patients who have received a bone marrow transplant, call 800-533-1710.
Container/Tube:
Preferred: Lavender top (EDTA)
Acceptable: Yellow top (ACD)
Specimen Volume: 3 mL
Collection Instructions:
1. Invert several times to mix blood.
2. Send whole blood specimen in original tube. Do not aliquot.
Specimen Stability Information: Ambient (preferred) 4 days/Refrigerated
Forms
1. PKLR Gene Sequencing Patient Information (T766) is required.
2. New York Clients: Informed consent is required. Document on the request form or electronic order that a copy is on file. The following documents are available:
Useful For
Aiding in the diagnosis of pyruvate kinase (PK) deficiency
Ascertaining a causative variant in the PKLR gene of patients with low or relatively low levels of erythrocytic PK enzymatic activity
Ascertaining carrier status of family members of individuals diagnosed with PK deficiency for genetic counseling purposes
Genetics Test Information
This test utilizes next-generation sequencing to detect single nucleotide and copy number variants in PKLR. See Method Description for additional details.
Identification of a disease-causing variant may assist with diagnosis, prognosis, clinical management, recurrence risk assessment, familial screening, and genetic counseling for pyruvate kinase deficiency.
Special Instructions
Reporting Name
PKLR Full Gene AnalysisSpecimen Type
VariesSpecimen Minimum Volume
1 mL
Specimen Stability Information
Specimen Type | Temperature | Time | Special Container |
---|---|---|---|
Varies | Varies |
Reject Due To
All specimens will be evaluated at Mayo Clinic Laboratories for test suitability.Reference Values
An interpretive report will be provided.
Day(s) Performed
Varies
Report Available
28 to 42 daysSpecimen Retention Time
Whole blood: 2 weeks (if available); Extracted DNA: 3 monthsPerforming Laboratory
Mayo Clinic Laboratories in RochesterCPT Code Information
81405
LOINC Code Information
Test ID | Test Order Name | Order LOINC Value |
---|---|---|
PKLRZ | PKLR Full Gene Analysis | 94212-8 |
Result ID | Test Result Name | Result LOINC Value |
---|---|---|
618935 | Test Description | 62364-5 |
618936 | Specimen | 31208-2 |
618937 | Source | 31208-2 |
618938 | Result Summary | 50397-9 |
618939 | Result | 82939-0 |
618940 | Interpretation | 59465-5 |
618941 | Additional Results | 82939-0 |
621816 | Resources | 99622-3 |
621817 | Additional Information | 48767-8 |
621818 | Method | 85069-3 |
621819 | Genes Analyzed | 82939-0 |
621820 | Disclaimer | 62364-5 |
621821 | Released By | 18771-6 |