UT Genetics Center
Molecular Diagnostic Laboratory
Forms:
Molecular Diagnostic Laboratory Requisition (.doc)
Neurological: Presymptomatic Testing Consent form(.doc)
Neurological: Diagnostic Testing Consent Form (.doc)
This laboratory provides DNA-based analysis for diagnosis and carrier status identification for a variety of disorders that include the following:
- Warfarin Metabolism Mutation Panel
- Plavix Metabolism Mutation Panel (.pdf)
- KRAS Gene Mutation Analysis (.pdf)
- JAK2 Mutation in Polycythemia Vera and Related Disorders
- Cystic Fibrosis-36
- Fragile X Syndrome (FMR1)
- Hereditary Hemochromatosis (HFE C282Y & H63D Mutations)
- Huntington Disease
- Huntington Disease-like-2
- Y Deletion in Infertility
- Prader Willi Disorder
- Angelman Syndrome
- BCR/ABL Rearrangement in Leukemia
- Thrombotic Risk Including:
Factor V Leiden (R506Q)
Factor II Prothrombin (G20210A)
MTHFR (C677T)
Plasminogen Activator Inhibitor (4G/5G)
Additional tests are outlined in the Molecular Diagnostic Laboratory Requisition)
New Laboratory Offerings (.pdf) 2/11
Interpretations and recommendations are provided by a board certified molecular geneticist.
The capability to analyze specimens for molecular mutations connected to genetic disorders changes rapidly. Contact the Genetics Center's molecular laboratory for information regarding the currently available tests.
Additional Forms:
Helpful CPT Coding Information (.doc)
Quick Links
The University of Tennessee Graduate School of Medicine
Division of Medical Genetics/ UT Genetics Center
UT Graduate School of Medicine
Building A, Suite 435
1930 Alcoa Highway
Knoxville, Tennessee 37920
Phone: 865.305.9030
Toll free: 1.800.325.3894
Fax: 865.305.6675