SUCLG1-Related Encephalomyopathic Form of Mitochondrial DNA Depletion Syndrome via the SUCLG1 Gene
Summary and Pricing
Test Method
Exome Sequencing with CNV DetectionTest Code | Test Copy Genes | Test CPT Code | Gene CPT Codes Copy CPT Code | Base Price | |
---|---|---|---|---|---|
11725 | SUCLG1 | 81479 | 81479,81479 | $990 | Order Options and Pricing |
Pricing Comments
Our favored testing approach is exome based NextGen sequencing with CNV analysis. This will allow cost effective reflexing to PGxome or other exome based tests. However, if full gene Sanger sequencing is desired for STAT turnaround time, insurance, or other reasons, please see link below for Test Code, pricing, and turnaround time information. If the Sanger option is selected, CNV detection may be ordered through Test #600.
An additional 25% charge will be applied to STAT orders. STAT orders are prioritized throughout the testing process.
Click here for costs to reflex to whole PGxome (if original test is on PGxome Sequencing platform).
Click here for costs to reflex to whole PGnome (if original test is on PGnome Sequencing platform).
The Sanger Sequencing method for this test is NY State approved.
For Sanger Sequencing click here.Turnaround Time
3 weeks on average for standard orders or 2 weeks on average for STAT orders.
Please note: Once the testing process begins, an Estimated Report Date (ERD) range will be displayed in the portal. This is the most accurate prediction of when your report will be complete and may differ from the average TAT published on our website. About 85% of our tests will be reported within or before the ERD range. We will notify you of significant delays or holds which will impact the ERD. Learn more about turnaround times here.
Targeted Testing
For ordering sequencing of targeted known variants, go to our Targeted Variants page.
Clinical Features and Genetics
Clinical Features
The mitochondrial DNA (mtDNA) Depletion Syndromes (MDSs) form a group of clinically and genetically heterogeneous diseases characterized by a quantitative abnormality of the mitochondrial genome in specific tissues (Suomalainen and Isohanni 2010; El-Hattab and Scaglia 2013).
The SUCLG1-related encephalomyopathic form of MDS is characterized by infantile-onset of hypotonia, muscle atrophy, severe psychomotor delay, progressive neurologic deterioration, lactic acidosis, and excretion of methylmalonic acid (Carrozzo et al. 2016; Ostergaard et al. 2007). Other clinical features may include feeding difficulties, gastroesophageal reflux, sensorineural hearing impairment, postnatal growth retardation, respiratory insufficiency, hepatopathy, and/or hypertrophic cardiomyopathy.
Genetics
The SUCLG1-related encephalomyopathic form of MDS is an autosomal recessive disorder caused by pathogenic variants in the SUCLG1 gene (Ostergaard et al. 2007). Missense changes are the the most frequently identified genetic defect in this gene, but nonsense, splicing site variants, and small deletions have also been reported (Human Gene Mutation Database).
Succinyl-coenzyme A (CoA) ligase is an enzyme of the citric acid cycle that catalyzes the reversible conversion of succinyl-CoA, phosphate, and ADP (or GDP) to succinate, coenzyme A (CoASH), and ATP (or GTP). This enzyme is composed of two subunits: an invariant alpha subunit encoded by SUCLG1 and a beta subunit encoded by either SUCLA2 or SUCLG2. Nucleotide specificity is determined by the beta subunit, resulting in the ADP- or GDP-forming isoforms of succinyl-CoA ligase, respectively.
The encephalomyopathic form of MDS may also be caused by defects in SUCLA2 or RRM2B (El-Hattab and Scaglia 2013). Although they result in similar phenotypes, defects in SUCLG1 are less frequently identified compared to SUCLA2 (Carrozzo et al. 2016).
Clinical Sensitivity - Sequencing with CNV PGxome
Clinical sensitivity is problematic to estimate due to the genetic heterogeneity associated with these disorders and the scarcity of documented cases. Analytical sensitivity may be high because all SUCGL1 causative variants reported to date are expected to be detected by direct sequencing of genomic DNA.
No gross deletions or duplications have been reported in SUCLG1 to date (Human Gene Mutation Database).
Testing Strategy
This test provides full coverage of all coding exons of the SUCLG1 gene plus 10 bases of flanking noncoding DNA in all available transcripts along with other non-coding regions in which pathogenic variants have been identified at PreventionGenetics or reported elsewhere. We define full coverage as >20X NGS reads or Sanger sequencing. PGnome panels typically provide slightly increased coverage over the PGxome equivalent. PGnome sequencing panels have the added benefit of additional analysis and reporting of deep intronic regions (where applicable).
Dependent on the sequencing backbone selected for this testing, discounted reflex testing to any other similar backbone-based test is available (i.e., PGxome panel to whole PGxome; PGnome panel to whole PGnome).
Indications for Test
Candidates for this test are patients with the encephalomyopathic form of MDS, particularly individuals lacking pathogenic variants in SUCLA2. Testing is also indicated for family members of patients who have known SUCLG1 mutations. This test may also be considered for the reproductive partners of individuals who carry pathogenic variants in SUCLG1.
Candidates for this test are patients with the encephalomyopathic form of MDS, particularly individuals lacking pathogenic variants in SUCLA2. Testing is also indicated for family members of patients who have known SUCLG1 mutations. This test may also be considered for the reproductive partners of individuals who carry pathogenic variants in SUCLG1.
Gene
Official Gene Symbol | OMIM ID |
---|---|
SUCLG1 | 611224 |
Inheritance | Abbreviation |
---|---|
Autosomal Dominant | AD |
Autosomal Recessive | AR |
X-Linked | XL |
Mitochondrial | MT |
Disease
Name | Inheritance | OMIM ID |
---|---|---|
Mitochondrial DNA Depletion Syndrome 9 (Encephalomyopathic With Methylmalonic Aciduria) | AR | 245400 |
Citations
- Carrozzo R. et al. 2016. Journal of Inherited Metabolic Disease. 39:243-52. PubMed ID: 26475597
- El-Hattab A.W. and Scaglia F. 2013. Neurotherapeutics. 10:186-98. PubMed ID: 23385875
- Human Gene Mutation Database (Bio-base).
- Ostergaard E. et al. 2007. American Journal of Human Genetics. 81:383-7. PubMed ID: 17668387
- Suomalainen A. and Isohanni P. et al. 2010. Neuromuscular Disorders. 20:429-37. PubMed ID: 20444604
Ordering/Specimens
Ordering Options
We offer several options when ordering sequencing tests. For more information on these options, see our Ordering Instructions page. To view available options, click on the Order Options button within the test description.
myPrevent - Online Ordering
- The test can be added to your online orders in the Summary and Pricing section.
- Once the test has been added log in to myPrevent to fill out an online requisition form.
- PGnome sequencing panels can be ordered via the myPrevent portal only at this time.
Requisition Form
- A completed requisition form must accompany all specimens.
- Billing information along with specimen and shipping instructions are within the requisition form.
- All testing must be ordered by a qualified healthcare provider.
For Requisition Forms, visit our Forms page
If ordering a Duo or Trio test, the proband and all comparator samples are required to initiate testing. If we do not receive all required samples for the test ordered within 21 days, we will convert the order to the most effective testing strategy with the samples available. Prior authorization and/or billing in place may be impacted by a change in test code.
Specimen Types
Specimen Requirements and Shipping Details
PGxome (Exome) Sequencing Panel
PGnome (Genome) Sequencing Panel
ORDER OPTIONS
View Ordering Instructions1) Select Test Type
2) Select Additional Test Options
No Additional Test Options are available for this test.