Single Gene Sequencing tests in Dubai & UAE

Compare available Single Gene Sequencing tests, their listed prices and the information provided for each option. Test selection and preparation should be discussed with your clinician.

Tests in this category

297

Listed price range

2,800.00–4,000.00 AED

Clinical preparation

Confirm test-specific instructions with your clinician or laboratory.

Compare available tests

Single Gene Sequencing test prices

Showing 151–165 of 297 matching tests.

Single Gene Sequencing diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-5098 KRT9 Gene Epidermolytic Palmoplantar Keratoderma Genetic Test This genetic test identifies pathogenic variants in the KRT9 gene associated with epidermolytic palmoplantar keratoderma (EPPK).	Whole Blood (3 mL) or FTA Card Dried Blood Spot	3 – 4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the KRT9 gene"] Parameters [] Preparation ["No fasting required"] Indications ["Suspected diagnosis of Epidermolytic Palmoplantar Keratoderma (EPPK)", "Family history of EPPK", "Differential diagnosis of palmoplantar keratodermas"] Measurement technique Confirm with laboratory Codes LOINC: 83025-8 ICD-10: Q82.8 Clinical summary This genetic test identifies pathogenic variants in the KRT9 gene associated with epidermolytic palmoplantar keratoderma (EPPK).
TEST-6085 L2HGDH Gene L-2-Hydroxyglutaric Aciduria Genetic Test This test evaluates the L2HGDH gene for mutations associated with L-2-hydroxyglutaric aciduria.	Whole Blood, FTA Card, Buccal Swab, or Extracted DNA	3–4 Weeks (expedited available)	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["L2HGDH gene sequence", "Copy Number Variations (CNV) in L2HGDH gene"] Parameters [] Preparation ["No specific fasting required", "Avoid sample collection during active febrile illness"] Indications ["Suspected L-2-hydroxyglutaric aciduria", "Confirmation of diagnosis", "Family history of L-2-hydroxyglutaric aciduria"] Measurement technique Confirm with laboratory Codes LOINC: 94222-8 ICD-10: E72.3 Clinical summary This test evaluates the L2HGDH gene for mutations associated with L-2-hydroxyglutaric aciduria.
TEST-6215 LARS2 Gene Sequencing (Hydrops, Lactic Acidosis, and Sideroblastic Anemia) NGS Test This test identifies pathogenic variants in the LARS2 gene, which are associated with the rare syndromic triad of hydrops fetalis, lactic acidosis, and sideroblastic anemia (HLASA)...	Whole blood (EDTA tube), extracted DNA, or FTA card	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["LARS2 gene variants", "Single nucleotide variants", "Small insertions/deletions", "Splice-site alterations"] Parameters [] Preparation ["No specific fasting required", "Do not discontinue prescribed medication without physician instruction"] Indications ["Non-immune hydrops fetalis", "Unexplained lactic acidosis", "Sideroblastic anaemia unresponsive to standard therapy"] Measurement technique Confirm with laboratory Codes LOINC: 83795-8 ICD-10: D64.0 Clinical summary This test identifies pathogenic variants in the LARS2 gene, which are associated with the rare syndromic triad of hydrops fetalis, lactic acidosis, and sideroblastic anemia (HLASA).
TEST-3446 LAS1L Gene Wilson-Turner Syndrome Genetic Test This genetic test analyzes the LAS1L gene to detect pathogenic variants associated with Wilson-Turner syndrome.	Peripheral whole blood, extracted DNA, or dried blood spot on FTA card	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the LAS1L gene", "Sequence variants in coding exons and splice sites"] Parameters [] Preparation [] Indications ["Suspected Wilson-Turner syndrome based on clinical presentation", "Family history of Wilson-Turner syndrome", "Need for accurate recurrence risk counseling"] Measurement technique Confirm with laboratory Codes LOINC: 93478-2 ICD-10: Q87.8, E34.8 Clinical summary This genetic test analyzes the LAS1L gene to detect pathogenic variants associated with Wilson-Turner syndrome.
TEST-2661 LEFTY2 Gene Left-Right Axis Malformations Genetic Test This test identifies pathogenic variants in the LEFTY2 gene associated with left-right axis malformations.	Whole blood (EDTA), extracted DNA, or FTA card	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["LEFTY2 gene coding region variants", "Pathogenic variants linked to laterality defects"] Parameters [] Preparation ["No specific fasting required", "Inform phlebotomist of anticoagulant therapy"] Indications ["Infants, children, or adults with clinical features suggestive of laterality defects", "Confirmation of molecular cause for left-right axis malformations"] Measurement technique Confirm with laboratory Codes LOINC: 21636-6 ICD-10: Q89.3, Q20.8 Clinical summary This test identifies pathogenic variants in the LEFTY2 gene associated with left-right axis malformations.
TEST-5349 LEMD3 Gene Buschke-Ollendorff Syndrome Genetic Test This test evaluates the LEMD3 gene for pathogenic variants associated with Buschke-Ollendorff syndrome.	Whole Blood or Buccal Swab	3–4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the LEMD3 gene"] Parameters [] Preparation ["No fasting or special preparation needed"] Indications ["Suspected Buschke-Ollendorff syndrome", "Differentiation of osteopoikilosis from sclerotic metastases"] Measurement technique Confirm with laboratory Codes LOINC: 101368-6 ICD-10: Q78.8 Clinical summary This test evaluates the LEMD3 gene for pathogenic variants associated with Buschke-Ollendorff syndrome.
TEST-4841 LIG4 Gene (LIG4 Syndrome) Genetic Test This genetic test identifies pathogenic variants in the LIG4 gene, which are responsible for LIG4 syndrome.	Peripheral whole blood (EDTA)	21–28 calendar days	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["LIG4 gene sequence", "Pathogenic variants (SNVs, indels, CNVs)"] Parameters [{"name": "Sensitivity", "reference_range": ">99.9% for SNVs, indels, CNVs"}] Preparation [] Indications ["Suspected LIG4 syndrome", "Syndromic combined immunodeficiency", "Microcephaly", "Photosensitivity", "Family history of lymphoma or leukaemia", "Carrier testing for at-risk family members"] Measurement technique Confirm with laboratory Codes LOINC: 101370-8 ICD-10: D81.8 Clinical summary This genetic test identifies pathogenic variants in the LIG4 gene, which are responsible for LIG4 syndrome.
TEST-4305 LMNA Gene Dilated Cardiomyopathy with Hypergonadotropic Hypogonadism Genetic Testing Test This genetic test analyzes the LMNA gene for variants associated with dilated cardiomyopathy and hypergonadotropic hypogonadism.	Peripheral whole blood (or saliva as alternative)	3–4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["LMNA gene sequence variants", "Pathogenic/Likely Pathogenic mutations"] Parameters [] Preparation ["No specific fasting required", "Inform lab of any medications"] Indications ["Diagnosis confirmation", "Family cascade screening", "Risk assessment", "Guiding clinical management"] Measurement technique Confirm with laboratory Codes LOINC: 82939-0 ICD-10: I42.0, E29.1 Clinical summary This genetic test analyzes the LMNA gene for variants associated with dilated cardiomyopathy and hypergonadotropic hypogonadism.
TEST-3936 LZTFL1 Gene Bardet‑Biedl Syndrome Genetic Test This genetic test analyzes the LZTFL1 gene for pathogenic variants associated with Bardet-Biedl syndrome.	Peripheral Whole Blood (EDTA)	3 to 4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["LZTFL1 gene coding region", "Single-nucleotide variants", "Small insertions/deletions", "Copy-number alterations"] Parameters [] Preparation [] Indications ["Clinical features of Bardet-Biedl syndrome", "Documented family history of Bardet-Biedl syndrome"] Measurement technique Confirm with laboratory Codes LOINC: 94305-9 ICD-10: Q87.89 Clinical summary This genetic test analyzes the LZTFL1 gene for pathogenic variants associated with Bardet-Biedl syndrome.
TEST-4776 MAFB Gene Test This test identifies pathogenic variants in the MAFB gene, confirming a diagnosis of Multicentric Carpotarsal Osteolysis Syndrome (MCTO).	Peripheral whole blood or Dried Blood Spot (DBS) on FTA card	3–4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the MAFB gene", "Coding regions and splice sites of the MAFB gene"] Parameters [] Preparation ["No specific fasting required.", "No medication adjustments needed unless advised by your doctor."] Indications ["Suspected Multicentric Carpotarsal Osteolysis Syndrome (MCTO)", "Progressive joint pain and swelling in hands and feet"] Measurement technique Confirm with laboratory Codes LOINC: 81247-9 ICD-10: M89.51 Clinical summary This test identifies pathogenic variants in the MAFB gene, confirming a diagnosis of Multicentric Carpotarsal Osteolysis Syndrome (MCTO).
TEST-3685 MAGT1 Gene Immunodeficiency, X-Linked, with Magnesium Defect, Epstein-Barr Virus Infection and Neoplasia Genetic Test This genetic test analyzes the MAGT1 gene to identify mutations associated with X-linked immunodeficiency, magnesium defects, and susceptibility to Epstein-Barr virus infections an...	Peripheral Whole Blood (EDTA) or Dried Blood Spot (FTA Card)	3 to 4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["MAGT1 gene sequence", "Presence of pathogenic variants"] Parameters [] Preparation ["No fasting required", "No medication changes required", "Pre-genetic counselling session mandatory"] Indications ["Clinical suspicion of X-linked immunodeficiency with magnesium defect", "Family history of MAGT1-related disorders"] Measurement technique Confirm with laboratory Codes LOINC: 61330-7 ICD-10: D81.8 Clinical summary This genetic test analyzes the MAGT1 gene to identify mutations associated with X-linked immunodeficiency, magnesium defects, and susceptibility to Epstein-Barr virus infections and neoplasia.
TEST-3149 MASTL Gene Thrombocytopenia Type 2 Genetic Test This genetic test identifies pathogenic variants in the MASTL gene associated with autosomal recessive thrombocytopenia type 2.	Whole blood (EDTA), extracted DNA, or FTA card	21–28 Days	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the MASTL gene", "Coverage of coding regions and splice sites"] Parameters [] Preparation ["No fasting required", "Genetic counselling session mandatory", "Informed consent required"] Indications ["Suspected inherited thrombocytopenia", "Family history of thrombocytopenia", "Differentiation from immune or acquired thrombocytopenia", "Genetic counseling and family screening"] Measurement technique Confirm with laboratory Codes LOINC: 90556-0 ICD-10: D69.4 Clinical summary This genetic test identifies pathogenic variants in the MASTL gene associated with autosomal recessive thrombocytopenia type 2.
TEST-2573 MCPH1 Gene Microcephaly, Autosomal Recessive Type 1 Genetic Test This genetic test identifies pathogenic variants in the MCPH1 gene, the primary cause of autosomal recessive primary microcephaly type 1.	Whole Blood (3-5 mL EDTA) or Buccal Swab or FTA Card	3-4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in MCPH1 gene", "Copy number variations in MCPH1 gene"] Parameters [] Preparation ["No dietary or pharmacological restrictions apply", "Avoid contamination with heparin or gel-separator tubes if collecting whole blood"] Indications ["Suspected autosomal recessive primary microcephaly type 1", "Family history of microcephaly", "Genetic counselling for reproductive planning"] Measurement technique Confirm with laboratory Codes LOINC: 21635-9 ICD-10: Q02 Clinical summary This genetic test identifies pathogenic variants in the MCPH1 gene, the primary cause of autosomal recessive primary microcephaly type 1.
TEST-4017 MCTP2 Gene Coarctation of the Aorta Genetic Test This test detects pathogenic variants in the MCTP2 gene, a primary cause of coarctation of the aorta.	Peripheral Whole Blood, Extracted DNA, FTA Card	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the MCTP2 gene", "Copy number assessment of the MCTP2 gene"] Parameters [] Preparation ["No specific fasting required", "Inform phlebotomist of any medications"] Indications ["Diagnosis of coarctation of the aorta", "Family cascade screening for MCTP2 variants", "Personalized cardiovascular management"] Measurement technique Confirm with laboratory Codes LOINC: 94301-0 ICD-10: Q25.1 Clinical summary This test detects pathogenic variants in the MCTP2 gene, a primary cause of coarctation of the aorta.
TEST-2598 MED13L Gene Analysis (Mental Retardation, Facial Dysmorphism, Cardiac Defects) Test This test evaluates the MED13L gene for pathogenic variants associated with intellectual disability, facial dysmorphism, and cardiac defects.	Whole Blood (Peripheral Venipuncture)	3–4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the MED13L gene", "Single Nucleotide Variants (SNVs)", "Insertions/Deletions (Indels)", "Splice-site variants"] Parameters [] Preparation ["No specific fasting required", "Inform phlebotomist of any medications"] Indications ["Suspected MED13L-related disorder", "Developmental delay with dysmorphic features", "Congenital heart defects with developmental delay", "Family history of MED13L-related disorders"] Measurement technique Confirm with laboratory Codes LOINC: 99566-9 ICD-10: Q87.8, F70 Clinical summary This test evaluates the MED13L gene for pathogenic variants associated with intellectual disability, facial dysmorphism, and cardiac defects.

Category overview

Single Gene Sequencing: overview

Achieving a definitive diagnosis for a monogenic disorder often requires reading the entire genetic code of a specific gene to find elusive errors. As an elite subspecialty within our Genetics department, Single Gene Sequencing expansively scans the entirety of a single targeted gene to uncover rare or novel mutations. Utilizing state-of-the-art diagnostic technology, this comprehensive molecular screening provides the critical clarity needed to establish a firm diagnosis, safely guiding customized medical management and targeted therapeutic interventions. Consistently ranked among the top diagnostic labs in the UAE, DNA Labs guarantees the utmost in patient confidentiality, uncompromising analytical accuracy, and prompt, reliable reporting. Find the clear, definitive answers you need—schedule your single gene sequencing testing in UAE, arrange a comfortable home sample collection, or contact our specialized medical genetics professionals.

Before booking

Use the test details as a conversation starter

The right diagnostic option depends on your reason for testing and individual circumstances. Check the listed specimen and timing, then confirm any preparation requirements with the ordering clinician or laboratory before collection.