ATP10A Gene Autism/Mental Retardation/Angelman Syndrome, Susceptibility to, ATP10A Related NGS Genetic Test
Short Name: ATP10A Related NGS Genetic Test
Also known as: ATP10A Gene Autism/Mental Retardation/Angelman Syndrome Susceptibility Test, ATP10A Related NGS Genetic Test, ATP10A Gene Sequencing Test
ATP10A Gene Autism/Mental Retardation/Angelman Syndrome, Susceptibility to, ATP10A Related NGS Genetic Test test available at DNA Labs India for ₹20,000. Uses NGS Technology on Blood or Extracted DNA or One Drop Blood on FTA Card samples. Results in The genetic test report is usually available within 3 to 4 weeks after the sample reaches the laboratory.. Free home collection in 300+ cities across India.
🩺 Medically Reviewed By
Dr SULOCHANA HEMCHANDRA HOLLA
Consultant Medical Geneticist · Reg: 8532
Last reviewed: September 7, 2026
Overview
To identify pathogenic or likely pathogenic variants in the ATP10A gene that may increase susceptibility to autism spectrum disorder, intellectual disability, and Angelman syndrome, and to provide information for diagnosis, risk assessment, and genetic counseling.
- Test Code
- 3937
- Price
- ₹20,000
- Sample Type
- Blood or Extracted DNA or One Drop Blood on FTA Card
- Result Time
- The genetic test report is usually available within 3 to 4 weeks after the sample reaches the laboratory.
- Fasting Required
- No
- Method
- NGS Technology
Sample Collection
No fasting is required. A pre-test genetic counseling session is recommended to draw a pedigree chart of family members affected with ATP10A-related neurodevelopmental disorders. Please carry clinical history, referral notes, previous investigation reports, and any prior genetic testing records.
Method: Venipuncture or FTA card blood spot
Laboratory Analysis
A blood sample will be collected by venipuncture, or a one-drop blood sample will be collected on an FTA card. The procedure is quick and minimally invasive.
Report Delivery
You can resume routine activities immediately. If you experience excessive bleeding, swelling, or signs of infection at the puncture site, contact your physician.
Timeline: The genetic test report is usually available within 3 to 4 weeks after the sample reaches the laboratory.
Patient Instructions
About This Test
Who Should Get This Test
To identify pathogenic or likely pathogenic variants in the ATP10A gene that may increase susceptibility to autism spectrum disorder, intellectual disability, and Angelman syndrome, and to provide information for diagnosis, risk assessment, and genetic counseling.
How to Prepare
- Maintain the sample at ambient room temperature for FTA cards
- Use only the provided blood collection tube for blood sampling
- Label the sample clearly with patient name, unique ID, and collection time
- Ensure the sample reaches the laboratory within the required transport time
- Avoid exposing the FTA card to direct sunlight or high temperature
Doctor's Notes
Reviewed by Dr SULOCHANA HEMCHANDRA HOLLA — MBBS, MD (Medical Genetics) · Reg. No. 8532
"Clinical correlation is essential because ATP10A variants may act as susceptibility factors rather than definitive causes. A multidisciplinary approach with neurology, pediatrics, clinical genetics, and obstetric/gynecologic counseling is recommended."
Last medically reviewed: September 7, 2026
Test Parameters & Specifications
Sample Stability
- Hemolyzed, clotted, or improper blood sample
- Insufficient or dry FTA blood spot
- Mislabeled specimen
- Sample not transported under recommended conditions
- Incomplete requisition form or no clinical history
Understanding Your Results
Pathogenic / Likely pathogenic
Supports increased susceptibility or possible contribution to the neurodevelopmental phenotype; may guide management and family testing.
Variant of uncertain significance (VUS)
Cannot be classified as benign or pathogenic at present; additional segregation or functional studies may be required.
No pathogenic variant detected
A clinically significant mutation in ATP10A was not identified; other genetic or non-genetic causes should be considered.
Consult your referring physician or a clinical geneticist if the test shows a pathogenic or likely pathogenic variant, a variant of uncertain significance is reported, symptoms persist despite a negative result, or you need help understanding recurrence risk and family planning options.
Limitations
- ⚠This test only analyzes the ATP10A gene and does not rule out other genetic causes
- ⚠Mutations in other genes associated with autism, intellectual disability, or Angelman syndrome will not be detected
- ⚠Large structural rearrangements, deep intronic variants, and methylation defects may not be detected unless additional testing is performed
- ⚠A variant of uncertain significance may be reported and require further family studies
- ⚠Result should always be interpreted alongside clinical features and pedigree information
Risks & Considerations
- ●Minor bruising at the venipuncture site
- ●Rare bleeding or hematoma
- ●Very rare infection at the puncture site
- ●Emotional or psychological impact of receiving a genetic test result
Interfering Factors
- ●Poor DNA quality or insufficient sample quantity
- ●Sample contamination during collection or processing
- ●NGS coverage gaps in certain gene regions
- ●Presence of pseudogenes or complex genomic rearrangements
- ●Very large deletions or structural variants may not be detected by standard NGS analysis
Compare With Similar Tests
| Test | ATP10A Gene Autism/Mental Retardation/Angelman Syndrome, Susceptibility to, ATP10A Related NGS Genetic Test | |||
|---|---|---|---|---|
| Comparison | ATP10A Gene Autism/Mental Retardation/Angelman Syndrome, Susceptibility to, ATP10A Related NGS Genetic Test |
Frequently Asked Questions
What is the ATP10A gene test?
What is the cost of the ATP10A gene NGS test at DNA Labs India?
What sample is needed for ATP10A gene NGS testing?
Do I need to fast before this test?
How long does the ATP10A NGS genetic test take?
Who should consider this ATP10A gene test?
Does a negative result rule out Angelman syndrome or autism?
Does the test include genetic counseling?
What does a pathogenic ATP10A variant mean?
Can this NGS test detect other genetic causes?
Is home sample collection available for this test?
How should the ATP10A gene test result be used?
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