Genetics
Single Gene Analysis Tests in Dubai & UAE
Investigations in this area, with the specimen type, turnaround time and listed price for each option — so you and your clinician can compare before you book.
- Quality-controlled laboratory
- Home collection across the UAE
- Confidential handling of results
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Single Gene Analysis investigations
All 26 investigations in this category are listed below.
| Test | What it measures | Specimen | Turnaround | Price | Book |
|---|---|---|---|---|---|
| AMTN Gene Amelotin Deficiency Genetic Test TEST-5388 LOINC 82301-8 | This genetic test identifies pathogenic variants in the AMTN gene associated with amelogenesis imperfecta and related syndromes. | Whole Blood (EDTA/FTA Card) or Extracted DNA | 3-4 Weeks | 2,800.00 AED | Details |
| ARX Gene-Associated Agenesis of Corpus Callosum with Abnormal Genitalia (XLAG) Genetic Test TEST-2937 LOINC 80230-8 | This diagnostic test evaluates the ARX gene for pathogenic variants associated with X-linked lissencephaly with ambiguous genitalia (XLAG) syndrome an... | Peripheral whole blood (3–5 mL venipuncture) or finger-prick blood spot | 3–4 Weeks | 2,800.00 AED | Details |
| CANT1 Gene Desbuquois Dysplasia Type 1 Genetic Test TEST-2884 LOINC 94233-4 | This test identifies pathogenic variants in the CANT1 gene associated with Desbuquois dysplasia type 1. | Peripheral Whole Blood, Extracted DNA, or FTA Card | 3–4 weeks | 2,800.00 AED | Details |
| CD320 Gene (Methylmalonic Aciduria, cblR Type) Genetic Test TEST-5982 LOINC 81214-4 | This genetic test analyzes the CD320 gene to detect mutations associated with methylmalonic aciduria, cblR type. | Peripheral whole blood, extracted DNA, or dried blood spot (FTA card) | 3–4 Weeks | 2,800.00 AED | Details |
| COQ2 Gene Coenzyme Q10 Deficiency Type 1 Genetic Test TEST-4079 LOINC 97943-6 | This genetic test identifies pathogenic variants in the COQ2 gene associated with primary coenzyme Q10 deficiency type 1. | Peripheral Whole Blood (3–5 mL venous blood or FTA card) | 3-4 Weeks | 2,800.00 AED | Details |
| CRHR1 Gene Pulmonary Newborn Hypertension Genetic Test TEST-4125 LOINC 21636-6 | This test evaluates the CRHR1 gene for pathogenic variants associated with persistent pulmonary hypertension in newborns (PPHN). | Whole Blood or FTA Card | 3-4 Weeks | 2,800.00 AED | Details |
| CSTA Gene Peeling Skin Syndrome Type 4 Genetic Test TEST-4640 LOINC 55231-1 | This test identifies pathogenic variants in the CSTA gene associated with Peeling Skin Syndrome Type 4. | Peripheral Whole Blood, Extracted DNA, or Dried Blood Spot on FTA Card | 3–4 Weeks | 2,800.00 AED | Details |
| CYBB Gene (Chronic Granulomatous Disease, X‑Linked) Genetic Test TEST-5045 LOINC 21636-5 | This genetic test evaluates the CYBB gene for pathogenic variants associated with X-linked Chronic Granulomatous Disease (CGD). | Peripheral whole blood (EDTA) | 3–4 weeks | 2,800.00 AED | Details |
| DVL1 Gene (Robinow Syndrome, Autosomal Dominant Type 2) Genetic Test TEST-2375 LOINC 21636-6 | This test detects pathogenic variants in the DVL1 gene associated with autosomal dominant Robinow syndrome type 2. | Peripheral Whole Blood (EDTA tube) or Capillary Blood on FTA Card | 3 – 4 Weeks | 2,800.00 AED | Details |
| DYNC1H1 Gene Intellectual Disability, Autosomal Dominant 13 (MRD13) Genetic Test TEST-4905 LOINC 94219-1 | This genetic test identifies pathogenic variants in the DYNC1H1 gene, which are associated with autosomal dominant intellectual disability type 13 (MR... | Whole Blood (EDTA Tube) or Dried Blood Spot (FTA Card) | 3–4 weeks | 2,800.00 AED | Details |
| ERCC4 Gene Xeroderma Pigmentosum Group F Genetic Test TEST-4479 LOINC 21613-5 | This test identifies pathogenic variants in the ERCC4 gene associated with Xeroderma Pigmentosum Group F. | Peripheral whole blood (EDTA) or FTA dried blood spot | 3 to 4 weeks | 2,800.00 AED | Details |
| KDM6A Gene Kabuki Syndrome Type 2 Genetic Test TEST-2689 LOINC 94065-1 | This test evaluates the KDM6A gene for pathogenic variants associated with Kabuki syndrome type 2. | Peripheral whole blood, isolated DNA, or FTA card | 3–4 Weeks | 2,800.00 AED | Details |
| LARS2 Gene Hydrops, Lactic Acidosis, and Sideroblastic Anemia (HLASA) Genetic Test TEST-3260 LOINC 94266-3 | This test identifies pathogenic variants in the LARS2 gene, confirming the diagnosis of Hydrops, Lactic Acidosis, and Sideroblastic Anemia (HLASA) syn... | Peripheral Whole Blood, Extracted DNA, or FTA Card | 3–4 Weeks | 2,800.00 AED | Details |
| LPIN1 Gene Myoglobinuria Acute Recurrent Genetic Test TEST-4022 LOINC 74807-9 | This genetic test evaluates the LPIN1 gene for pathogenic variants associated with autosomal recessive recurrent myoglobinuria. | Whole blood, extracted DNA, or FTA card | 21–28 working days | 2,800.00 AED | Details |
| MMP14 Gene Winchester Syndrome Genetic Test TEST-4468 LOINC 21619-0 | This test identifies pathogenic variants in the MMP14 gene associated with Winchester syndrome. | Peripheral whole blood (EDTA), extracted genomic DNA, or dried blood spot (FTA card) | 3–4 weeks standard; 2–week express option available | 2,800.00 AED | Details |
| MRPS16 Gene Test TEST-6148 LOINC 82545-9 | This test identifies pathogenic variants in the MRPS16 gene associated with Combined Oxidative Phosphorylation Deficiency Type 2 (COXPD2). It utilizes... | Peripheral Blood (Whole Blood, EDTA) | 3–4 Weeks | 2,800.00 AED | Details |
| NIPAL4 Gene (Congenital Ichthyosiform Erythroderma, Nonbullous Type 1) Genetic Test TEST-4996 LOINC 48018-6 | This genetic test identifies mutations in the NIPAL4 gene associated with nonbullous congenital ichthyosiform erythroderma. | Peripheral Whole Blood, Extracted DNA, or FTA Card Blood Spot | 3–4 Weeks | 2,800.00 AED | Details |
| PREPL Gene Cystinuria Genetic Test TEST-3854 LOINC 81260-9 | This test identifies pathogenic mutations in the PREPL gene associated with hypotonia-cystinuria syndrome. | Peripheral Whole Blood (EDTA) | 21–28 Working Days | 2,800.00 AED | Details |
| SIX5 Gene Branchio-Oto-Renal (BOR) Syndrome Type 2 Genetic Test TEST-3502 LOINC 81247-9 | This test identifies pathogenic variants in the SIX5 gene to diagnose Branchio-Oto-Renal (BOR) syndrome type 2. | Peripheral whole blood | 3 to 4 weeks | 2,800.00 AED | Details |
| TANC2 Gene NGS Test for Brain Disorders TEST-2263 LOINC 95900-9 | The TANC2 Gene NGS Test detects pathogenic variants in the TANC2 gene associated with neurodevelopmental disorders. | Peripheral whole blood or buccal swab | 3–4 weeks | 2,800.00 AED | Details |
| TMLHE Gene Sequencing for X-Linked Autism Susceptibility Type 6 (NGS) Test TEST-3907 LOINC 51995-8 | This diagnostic test evaluates the TMLHE gene for pathogenic variants associated with X-linked autism susceptibility type 6. | Peripheral Whole Blood (EDTA) or Saliva Sample | 14–21 Working Days (3–4 Weeks) | 2,800.00 AED | Details |
| TP63 Gene Ectrodactyly-Ectodermal Dysplasia-Cleft Lip/Palate Syndrome Type 3 (EEC3) Genetic Test TEST-2862 LOINC 21636-6 | This genetic test analyzes the TP63 gene to detect mutations associated with Ectrodactyly-Ectodermal Dysplasia-Cleft Lip/Palate Syndrome Type 3 (EEC3)... | Peripheral Whole Blood (EDTA tube), Buccal Swab, or FTA Card | 3–4 weeks | 2,800.00 AED | Details |
| TTC7A Gene Sequencing Test TEST-2704 LOINC 81255-6 | This test evaluates the TTC7A gene for pathogenic variants linked to multiple intestinal atresia and combined immunodeficiency. | Whole blood, DNA, or dry blood spot (FTA card) | 3–4 Weeks | 2,800.00 AED | Details |
| TUBB3 Gene Cortical Dysplasia, Complex, With Other Brain Malformations Type 1 Genetic Test TEST-4147 LOINC 81313-5 | This test identifies pathogenic variants in the TUBB3 gene associated with complex cortical dysplasia with other brain malformations type 1 (CDCBM1). | Peripheral Whole Blood | 3–4 weeks | 2,800.00 AED | Details |
| ZIC2 Gene Holoprosencephaly Type 5 Genetic Test TEST-2743 LOINC 21636-6 | This diagnostic test evaluates the ZIC2 gene for pathogenic variants associated with holoprosencephaly type 5. | Whole Blood (EDTA), DNA, FTA Card | 3–4 weeks | 2,800.00 AED | Details |
| ZNF778 Gene-Associated Autism: Genetic Test TEST-3949 LOINC 21636-6 | This test identifies pathogenic variants in the ZNF778 gene associated with autism spectrum disorder. | Peripheral whole blood or dried blood spot (FTA card) | 3–4 weeks | 2,800.00 AED | Details |
Clinical overview
About Single Gene Analysis
Before your appointment
Preparation & sample collection
Follow the instructions you are given
Fasting, timing and medicine restrictions differ between investigations. The instructions for your specific request are confirmed when you book.
Bring your identification
A valid photo ID is required at collection so that your sample is matched correctly to your record.
Tell us about medicines
Prescription medicines, supplements and recent procedures can affect how an investigation is scheduled or interpreted — please mention them.
Ask before collection
If anything about preparation is unclear, contact us before your appointment. Preparation errors can affect reporting times.
Patient information
Frequently asked questions
Practical answers about Single Gene Analysis testing at DNA Labs UAE. This information is general and does not replace advice from your treating clinician.
How do I choose the right Single Gene Analysis test?
The correct investigation depends on what your clinician is trying to establish. Review the specimen type and turnaround time below, then confirm the choice with your treating doctor before booking.
What specimen is required?
Specimen requirements are listed for each investigation. If a request involves more than one sample type, our team will confirm what is needed at the time of booking.
Do you offer home sample collection in Dubai and the UAE?
Yes. Home collection can be arranged across Dubai and the wider UAE. Availability and appointment windows vary by location, so please confirm when you book.
How long do results take?
Turnaround depends on the investigation and the method used. The expected reporting time is confirmed with you before collection.
Is there anything I need to do before sample collection?
Some investigations require fasting, a specific collection time, or avoiding certain medicines or activities. Preparation details are shared when you book — please follow them and ask if anything is unclear.
How will I receive my report?
Reports are issued as secure digital documents and can be shared with your referring clinician on request. Please review results with a qualified clinician who can interpret them in context.
About this clinical information
The information on this Single Gene Analysis page describes laboratory investigations in general terms. It is written to help you understand what an investigation involves — it is not a diagnosis and it is not a substitute for advice from your treating clinician.
- Investigation names, specimen types and listed prices are reviewed against laboratory records.
- Preparation guidance is indicative — confirm test-specific instructions before collection.
- Content is updated when investigations, methods or reporting formats change.
- Results are released to the patient and, on request, shared with the referring clinician.
Medical disclaimer: This page is for general information and education only. It is not medical advice, diagnosis or treatment, and it does not replace a consultation with a qualified healthcare professional. Always seek the advice of your doctor or another qualified provider with any questions about a medical condition or before ordering a test.
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Tell us what your clinician has requested and we'll confirm availability, price, preparation and the most convenient collection option — including home collection in Dubai and across the UAE.
- Home collection available across the UAE
- Digital reports delivered securely
- Confidential handling of every request
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