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.

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Single Gene Sequencing test prices

Showing 181–195 of 297 matching tests.

Single Gene Sequencing diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-2291 NFIX Gene Sequencing for Sotos-Like Syndrome DNA Test This test identifies mutations in the NFIX gene, which are associated with Sotos-like syndrome, a rare genetic overgrowth disorder.	Whole Blood, Extracted DNA, or One Drop Blood on FTA Card	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["NFIX gene mutations", "Genetic variants associated with Sotos-like syndrome"] Parameters [] Preparation [] Indications ["Clinical suspicion of Sotos-like syndrome", "Evaluation of overgrowth syndromes", "Family planning guidance"] Measurement technique Confirm with laboratory Codes LOINC: 55233-1 ICD-10: Q87.3 Clinical summary This test identifies mutations in the NFIX gene, which are associated with Sotos-like syndrome, a rare genetic overgrowth disorder.
TEST-4583 NHEJ1 Gene NGS Test for SCID, Microcephaly & Radiation Sensitivity This test identifies pathogenic variants in the NHEJ1 gene associated with severe combined immunodeficiency (SCID), microcephaly, growth retardation, and radiation sensitivity.	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 ["NHEJ1 gene variants", "Pathogenic mutations"] Parameters [] Preparation ["No specific fasting required", "Inform lab of any recent blood transfusions or transplants"] Indications ["Suspected Severe Combined Immunodeficiency (SCID)", "Microcephaly with developmental delay", "Growth retardation", "Family history of NHEJ1-related disorders"] Measurement technique Confirm with laboratory Codes LOINC: 21636-6 ICD-10: D81.0, Q02 Clinical summary This test identifies pathogenic variants in the NHEJ1 gene associated with severe combined immunodeficiency (SCID), microcephaly, growth retardation, and radiation sensitivity.
TEST-5302 NIPBL Gene Cornelia de Lange Syndrome Type 1 Genetic Test This test identifies pathogenic variants in the NIPBL gene associated with Cornelia de Lange syndrome type 1.	Whole Blood, Extracted DNA, FTA Card 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 NIPBL gene", "Deletions and duplications in the NIPBL gene"] Parameters [] Preparation ["A pre-test genetic counseling session is mandatory.", "Legal guardian consent required for minors."] Indications ["Individuals showing clinical features of CdLS", "Confirmation of suspected CdLS diagnosis"] Measurement technique Confirm with laboratory Codes LOINC: 92821-0 ICD-10: Q87.1 Clinical summary This test identifies pathogenic variants in the NIPBL gene associated with Cornelia de Lange syndrome type 1.
TEST-2270 NKX3-2 Gene Spondylo-Megaepiphyseal-Metaphyseal Dysplasia Genetic Test This genetic test analyzes the NKX3-2 gene to detect mutations associated with Spondylo-megaepiphyseal-metaphyseal dysplasia (SMMD).	Whole blood, extracted DNA, or FTA card drop	3–4 weeks from sample receipt	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the NKX3-2 gene", "Point mutations", "Small insertions/deletions", "Copy number variations (CNVs)"] Parameters [] Preparation ["No fasting required"] Indications ["Suspected Spondylo-megaepiphyseal-metaphyseal dysplasia (SMMD)", "Family history of SMMD"] Measurement technique Confirm with laboratory Codes LOINC: 93268-5 ICD-10: Q77.8 Clinical summary This genetic test analyzes the NKX3-2 gene to detect mutations associated with Spondylo-megaepiphyseal-metaphyseal dysplasia (SMMD).
TEST-2778 NODAL Gene Heterotaxy Visceral Type 5 Genetic Test This test evaluates the NODAL gene for mutations associated with visceral heterotaxy type 5, a condition affecting organ positioning.	Peripheral Whole Blood (EDTA)	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["NODAL gene mutations", "Visceral heterotaxy type 5"] Parameters [] Preparation [] Indications ["Suspected visceral heterotaxy", "Complex congenital heart disease", "Situs ambiguus", "Asplenia"] Measurement technique Confirm with laboratory Codes LOINC: 82543-0 ICD-10: Q89.3 Clinical summary This test evaluates the NODAL gene for mutations associated with visceral heterotaxy type 5, a condition affecting organ positioning.
TEST-2446 NRXN1 Gene Sequencing for Pitt-Hopkins Syndrome (Genetic Test) This genetic test analyzes the NRXN1 gene to detect pathogenic variants associated with Pitt-Hopkins syndrome.	Peripheral Whole Blood	3 to 4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["NRXN1 gene sequence", "Pathogenic variants (point mutations, deletions, insertions)"] Parameters [] Preparation ["No special preparation required", "Inform phlebotomist of anticoagulant use"] Indications ["Suspected Pitt-Hopkins syndrome", "Confirmation of clinical diagnosis", "Genetic counseling"] Measurement technique Confirm with laboratory Codes LOINC: 21797-6 ICD-10: Q87.0 Clinical summary This genetic test analyzes the NRXN1 gene to detect pathogenic variants associated with Pitt-Hopkins syndrome.
TEST-4507 NTRK1 Gene HSAN4 Genetic Test This test evaluates the entire coding region and conserved splice sites of the NTRK1 gene to identify pathogenic variants associated with Hereditary Sensory and Autonomic Neuropath...	Peripheral whole blood (3–5 mL in EDTA lavender-top tube)	3–4 weeks (21–28 calendar days)	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the NTRK1 gene", "Single nucleotide variants (SNVs)", "Small insertions/deletions (indels)", "Canonical splice-site alterations"] Parameters [] Preparation ["No fasting required", "No medication adjustments required", "No special dietary preparations required", "Mandatory pre-test genetic counselling session"] Indications ["Suspected Hereditary Sensory and Autonomic Neuropathy Type IV (HSAN4)", "Congenital insensitivity to pain", "Autonomic dysfunction"] Measurement technique Confirm with laboratory Codes LOINC: 21647-5 ICD-10: G60.8, G90.0 Clinical summary This test evaluates the entire coding region and conserved splice sites of the NTRK1 gene to identify pathogenic variants associated with Hereditary Sensory and Autonomic Neuropathy Type IV (HSAN4).
TEST-3700 OCRL Gene Test This test evaluates the OCRL gene for pathogenic variants associated with Lowe syndrome (Oculocerebrorenal Syndrome). It identifies mutations responsible for the disorder's charact...	Peripheral Whole Blood	3 to 4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the OCRL gene", "Full gene coverage"] Parameters [] Preparation ["Genetic counselling is mandatory prior to sample collection", "Do not discontinue prescribed medications without consulting your doctor"] Indications ["Clinical suspicion of Lowe syndrome", "Family history of X-linked disorders", "Unexplained cataracts", "Renal tubular dysfunction", "Developmental delay"] Measurement technique Confirm with laboratory Codes LOINC: 81333-2 ICD-10: E72.03 Clinical summary This test evaluates the OCRL gene for pathogenic variants associated with Lowe syndrome (Oculocerebrorenal Syndrome). It identifies mutations responsible for the disorder's characteristic kidney, eye, and nervous system abnormalities.
TEST-5401 OFD1 Gene Oral-Facial-Digital Syndrome Type 1 Genetic Test This test sequences the entire coding region of the OFD1 gene to identify pathogenic variants responsible for Oral-Facial-Digital Syndrome Type 1.	Whole Blood / Extracted DNA / 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 OFD1 gene"] Parameters [{"name": "Diagnostic Sensitivity", "reference_range": ">99.9%"}, {"name": "Detection Rate (NGS)", "reference_range": ">99% Coding Variants incl. Deep Intronic Splice Sites"}, {"name": "Detection Rate (Sanger)", "reference_range": "~90% – Misses Large Deletions & Mosaicism"}] Preparation ["No fasting required", "No medication adjustments required"] Indications ["Individuals presenting with symptoms of Oral-Facial-Digital Syndrome Type 1", "At-risk female relatives of affected individuals"] Measurement technique Confirm with laboratory Codes LOINC: 82939-0 ICD-10: Q87.0 Clinical summary This test sequences the entire coding region of the OFD1 gene to identify pathogenic variants responsible for Oral-Facial-Digital Syndrome Type 1.
TEST-5276 P4HB Gene Cole-Carpenter Syndrome Type 1 Genetic Test This genetic test identifies pathogenic variants in the P4HB gene associated with Cole-Carpenter syndrome type 1.	Whole Blood, Extracted DNA, or FTA Card Specimen	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["P4HB gene pathogenic variants", "Collagen folding disruption"] Parameters [] Preparation [] Indications ["Diagnosis of Cole-Carpenter syndrome type 1", "Carrier testing", "Pedigree analysis"] Measurement technique Confirm with laboratory Codes LOINC: 92860-7 ICD-10: Q87.8 Clinical summary This genetic test identifies pathogenic variants in the P4HB gene associated with Cole-Carpenter syndrome type 1.
TEST-2462 PAX2 Gene Papillorenal Syndrome Genetic Test This genetic test identifies pathogenic variants in the PAX2 gene, which are associated with Papillorenal Syndrome.	Peripheral whole blood (EDTA), buccal swab, or FTA card	3 to 4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the PAX2 gene", "Copy Number Variants (CNVs) in PAX2"] Parameters [] Preparation ["No specific fasting required", "Inform lab of any medications"] Indications ["Confirmation of clinical diagnosis of Papillorenal Syndrome", "Guidance for nephrological and ophthalmological surveillance", "Family planning for individuals with a family history", "Detection of asymptomatic carriers"] Measurement technique Confirm with laboratory Codes LOINC: 85705-0 ICD-10: Q87.8, Q60.3, Q13.8 Clinical summary This genetic test identifies pathogenic variants in the PAX2 gene, which are associated with Papillorenal Syndrome.
TEST-2240 PAX9 Genetic Test for Tooth Agenesis (Oligodontia) This test identifies pathogenic variants in the PAX9 gene associated with selective tooth agenesis type 3 (STHAG3). It utilizes next-generation sequencing (NGS) for comprehensive a...	Whole Blood (EDTA) or FTA Card	3–4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["PAX9 gene variants", "Pathogenic mutations"] Parameters [] Preparation ["A mandatory genetic counselling session must be completed before sample collection", "Maintain all current prescribed therapies unless explicitly advised otherwise by your treating physician", "Discuss any changes with your doctor before sample collection"] Indications ["Individuals with unexplained absence of permanent teeth, particularly premolars and molars", "Family history of oligodontia", "Children with delayed dental eruption patterns suggestive of a genetic aetiology"] Measurement technique Confirm with laboratory Codes LOINC: 94222-1 ICD-10: K00.0 Clinical summary This test identifies pathogenic variants in the PAX9 gene associated with selective tooth agenesis type 3 (STHAG3). It utilizes next-generation sequencing (NGS) for comprehensive analysis.
TEST-4663 PC Gene Leigh Syndrome Genetic Test (Pyruvate Carboxylase Deficiency) This test identifies pathogenic variants in the PC gene associated with pyruvate carboxylase deficiency, a cause of Leigh syndrome.	Whole blood (EDTA), DNA FTA card, or extracted DNA	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 PC gene"] Parameters [] Preparation ["No fasting required", "Maintain regular medications unless directed otherwise"] Indications ["Suspected pyruvate carboxylase deficiency", "Leigh syndrome diagnosis", "Family screening for PC gene variants"] Measurement technique Confirm with laboratory Codes LOINC: 93683-6 ICD-10: G31.83 Clinical summary This test identifies pathogenic variants in the PC gene associated with pyruvate carboxylase deficiency, a cause of Leigh syndrome.
TEST-5443 PDE4D Gene Acrodysostosis Type 2 (ACRDYS2) Genetic Test This test identifies pathogenic variants in the PDE4D gene associated with Acrodysostosis Type 2.	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 ["PDE4D gene mutations", "Pathogenic variants"] Parameters [] Preparation ["Mandatory genetic counselling session prior to testing.", "Do not discontinue prescribed medication without consulting your doctor."] Indications ["Suspected Acrodysostosis Type 2", "Diagnosis of rare skeletal dysplasia"] Measurement technique Confirm with laboratory Codes LOINC: 87833-5 ICD-10: Q77.4 Clinical summary This test identifies pathogenic variants in the PDE4D gene associated with Acrodysostosis Type 2.
TEST-3045 PDGFRB Gene Basal Ganglia Calcification Type 4 Genetic Test This genetic test identifies pathogenic variants in the PDGFRB gene associated with idiopathic basal ganglia calcification type 4 (IBGC4).	Whole Blood (EDTA) 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 the PDGFRB gene", "Full coding region and splice sites of the PDGFRB gene"] Parameters [] Preparation ["No specific fasting required", "No medication or diet restrictions"] Indications ["Diagnosis of idiopathic basal ganglia calcification type 4 (IBGC4)", "Family cascade screening for IBGC4", "Evaluation of patients with unexplained neurological symptoms and brain calcifications"] Measurement technique Confirm with laboratory Codes LOINC: 95286-5 ICD-10: G23.8 Clinical summary This genetic test identifies pathogenic variants in the PDGFRB gene associated with idiopathic basal ganglia calcification type 4 (IBGC4).

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.

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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.