Mitochondrial Depletion NGS Panel

Test Information

This panel of 23 genes intended for patients with a diagnosis or clinical suspicion of Mitochondrial Depletion and is performed by next generation sequencing.

Turnaround Time

8 weeks

CPT Code(s)





  • ABAT
  • AGK
  • APTX
  • DNA2
  • FBXL4
  • GFER
  • MFN2
  • MGME1
  • MPV17
  • OPA1
  • OPA3
  • POLG
  • POLG2
  • RRM2B
  • SLC25A4
  • SPG7
  • SUCLA2
  • SUCLG1
  • TFAM
  • TK2
  • TWNK
  • TYMP

Clinical Information

This panel consists of 23 nuclear-encoded genes that have been associated with mitochondrial DNA depletion disorders. These nuclear genes are responsible for the maintenance of mitochondrial DNA, so dysfunction of this process can lead to multisystem involvement and tend to be progressive. Variants of these disorders include encephalomyopathic, myopathic, hepatocerebral, and neurogastrointestinal types. Common symptoms may include the following: muscle weakness/hypotonia; motor and developmental delays in early-onset cases; digestive problems such as IBS, diarrhea, and constipation or other dysmotility; neurological issues such as migraines, seizures, and strokes; dysautonomia; kidney disease, cardiomyopathy; liver disease; vision problems, especially ophthalmoplegia, and hearing loss; and fatigue. While the majority of nuclear mitochondrial disorders are inherited in an autosomal recessive pattern, some conditions demonstrate autosomal dominant inheritance. These conditions can occur in infancy or early childhood and typically have a poor prognosis. However, tremendous clinical variability exists among these disorders. List of Genes and Conditions


For patients with a specific suspected disorder, individual gene sequencing should be considered first. Molecular testing is useful to confirm the diagnosis and to identify the disease causing mutations within a family to allow for carrier testing and prenatal diagnosis.


Next Generation Sequencing


The current design of this panel covers all genes and the flanking intronic sequences. This method allows for analysis of greater than 98% of the targeted sequence for the detection of nucleotide substitutions and small deletions and duplications. Large deletions and duplications will not be detected by this panel. Mutations and variants identified on the panel are confirmed with Sanger sequencing. All novel and apparently pathogenic changes are reported when found within the coding region as well as within 10 basepairs of each intron/exon boundary for each gene. Promoter and 3' untranslated sequences are not included in the current analysis. It should be noted that the current protocol is not specifically designed to detect copy number alterations and single exon deletions may require additional follow-up to determine whether or not they represent technical artifacts. We recommend further array-based testing to more accurately address the concerns of dosage alterations. The Cytogenetic Laboratory at GGC offers a high resolution whole genome SNP microarray. The GGC Diagnostic Laboratory Directors are available for further consultation regarding the limitations of the NGS and array testing procedures.

Specimen Requirements

The preferred sample type is 3-5 ml of peripheral blood collected in an EDTA (purple top) tube. Extracted DNA and saliva are also accepted for this test. Saliva samples must be submitted in an approved saliva kit. Contact the lab to receive a saliva kit or to have one sent to your patient.

Transport Instructions

The specimen should be kept at room temperature and delivered via overnight shipping. If shipment is delayed by one or two days, the specimen should be refrigerated and shipped at room temperature. Do not freeze the specimen. Samples collected on Friday can be safely designated for Monday delivery.

Prenatal Testing Information

If the pathogenic mutation(s) are identified in an affected individual using this panel, prenatal diagnosis is available for future pregnancies. Sanger sequencing will be used for prenatal diagnosis when there is a known familial mutation. Additional fees for cell culture and maternal cell contamination may apply. Maternal cell contamination studies are required for all prenatal molecular tests. Contact the laboratory prior to sending a prenatal specimen.

Have Questions? Need Support?

Call our laboratory at 1-800-473-9411 or contact one of our Laboratory Genetic Counselors for assistance.
Robin Fletcher, MS, CGC
Falecia Thomas, MS, CGC
Alex Finley, MS, CGC

Lucy's Story

When our daughter Lucy had a metabolic crisis at 7 days old, we were shocked and devastated to find out that she was born with a rare genetic disorder (MSUD). Her newborn screening results did not make it back in time to prevent the crisis, and no one at our local hospital was familiar with the disease. They did not know how to treat her. Calls were made to Greenwood Genetic Center to confirm her diagnosis and guide her care. Dr. Champaigne and Ami...

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