Diagnostic options · UAE

Single Gene tests in Dubai & UAE

Compare available Single Gene 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

332

Listed price range

2,000.00–2,800.00 AED

Clinical preparation

Confirm test-specific instructions with your clinician or laboratory.

Compare available tests

Single Gene test prices

Showing 196–210 of 332 matching tests.

Single Gene diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-3998 MTMR14 Gene Centronuclear Myopathy Type 1 Genetic Test This genetic test detects mutations in the MTMR14 gene associated with autosomal recessive centronuclear myopathy type 1.	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 ["Pathogenic variants in the MTMR14 gene", "Full coding region and splice sites"] Parameters [{"name": "Sensitivity", "reference_range": "99.9%"}, {"name": "Specificity", "reference_range": "99.8%"}] Preparation ["Provide clinical history", "Attend pre-test genetic counselling session"] Indications ["Diagnosis of centronuclear myopathy type 1", "Carrier screening", "Family planning"] Measurement technique Confirm with laboratory Codes LOINC: 81247-9 ICD-10: G71.2 Clinical summary This genetic test detects mutations in the MTMR14 gene associated with autosomal recessive centronuclear myopathy type 1.
TEST-5999 MTR Gene Methylcobalamin Deficiency (CblG Type) Genetic Test This genetic test analyzes the MTR gene to identify pathogenic variants associated with methylcobalamin deficiency (CblG type). It provides a definitive molecular diagnosis for thi...	Peripheral whole blood (EDTA tube)	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["MTR gene sequence", "Pathogenic variants in MTR gene"] Parameters [] Preparation ["No fasting required", "No medication changes required for DNA analysis"] Indications ["Suspected methylcobalamin deficiency (CblG type)", "Family history of CblG type", "Carrier screening"] Measurement technique Confirm with laboratory Codes LOINC: 65853-3 ICD-10: E72.11 Clinical summary This genetic test analyzes the MTR gene to identify pathogenic variants associated with methylcobalamin deficiency (CblG type). It provides a definitive molecular diagnosis for this treatable inborn error of vitamin B12 metabolism.
TEST-2287 MTRR Gene Spina Bifida Folate-Sensitive Genetic Test This test evaluates the MTRR gene for variants associated with folate-sensitive neural tube defects like spina bifida.	Peripheral whole blood (FTA card or standard venipuncture)	3–4 Weeks (90% reports in 24 days)	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["MTRR gene variants", "Folate metabolism pathway"] Parameters [] Preparation [] Indications ["Risk assessment for folate-sensitive spina bifida", "Personalized folate supplementation guidance", "Reproductive planning in families with neural tube defect history"] Measurement technique Confirm with laboratory Codes LOINC: 81217-1 ICD-10: Z13.71, Q05.9 Clinical summary This test evaluates the MTRR gene for variants associated with folate-sensitive neural tube defects like spina bifida.
TEST-2642 MYBPC1 Gene Lethal Congenital Contracture Syndrome Type 4 Genetic Test This test detects pathogenic variants in the MYBPC1 gene associated with Lethal Congenital Contracture Syndrome Type 4 (LCCS4).	Whole Blood, Extracted DNA, or One Drop of Blood on 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 MYBPC1 gene"] Parameters [] Preparation [] Indications ["Newborns or infants presenting with multiple joint contractures", "Infants with muscle atrophy and respiratory insufficiency", "Family history of MYBPC1-related myopathy"] Measurement technique Confirm with laboratory Codes LOINC: 21633-5 ICD-10: Q68.8 Clinical summary This test detects pathogenic variants in the MYBPC1 gene associated with Lethal Congenital Contracture Syndrome Type 4 (LCCS4).
TEST-2849 MYCN Gene Feingold Syndrome Genetic Test This test evaluates the MYCN gene for pathogenic variants associated with Feingold syndrome.	Whole Blood (EDTA), Extracted DNA, 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 ["Pathogenic variants in MYCN gene", "SNVs", "Indels", "CNVs", "Deep intronic variants"] Parameters [] Preparation ["No fasting required", "No medication changes required", "Have clinical history and family pedigree ready"] Indications ["Suspected Feingold syndrome", "Family screening", "Reproductive planning"] Measurement technique Confirm with laboratory Codes LOINC: 92850-0 ICD-10: Q87.8 Clinical summary This test evaluates the MYCN gene for pathogenic variants associated with Feingold syndrome.
TEST-3665 MYOC (Myocilin) Glaucoma, Open Angle Type 1A Genetic Test This genetic test evaluates the MYOC gene for variants associated with primary open-angle glaucoma type 1A.	Peripheral whole blood (EDTA) or buccal swab	3–4 weeks from sample receipt	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["MYOC gene variants (SNVs, indels, CNVs)", "Copy Number Variations (CNVs) in MYOC gene"] Parameters [] Preparation ["No specific fasting required", "Inform phlebotomist of any medications"] Indications ["Individuals with a family history of early-onset glaucoma", "Individuals diagnosed with open-angle glaucoma before age 40", "Suspected hereditary glaucoma pattern"] Measurement technique Confirm with laboratory Codes LOINC: 21627-6 ICD-10: H40.11X0, H40.1110, H40.1120, H40.1130 Clinical summary This genetic test evaluates the MYOC gene for variants associated with primary open-angle glaucoma type 1A.
TEST-2521 NALCN Gene Test This test analyzes the NALCN gene for pathogenic variants associated with infantile neuroaxonal neurodegeneration with facial dysmorphism.	Peripheral whole blood (1–2 ml) or FTA card finger-prick	3–4 weeks from sample accession	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the NALCN gene", "Copy number variations within the NALCN gene"] Parameters [] Preparation ["No specific fasting required", "No medication adjustments needed prior to testing"] Indications ["Suspected infantile neuroaxonal neurodegeneration with facial dysmorphism", "Early-onset neurological disorder of unknown etiology", "Family history of NALCN-related disorders"] Measurement technique Confirm with laboratory Codes LOINC: 21637-3 ICD-10: G31.89 Clinical summary This test analyzes the NALCN gene for pathogenic variants associated with infantile neuroaxonal neurodegeneration with facial dysmorphism.
TEST-5052 NCF1 Gene Chronic Granulomatous Disease, Autosomal Recessive, Cytochrome b-Positive Type 1 Test This test identifies pathogenic variants in the NCF1 gene, confirming a diagnosis of autosomal recessive chronic granulomatous disease type 1.	Peripheral Blood, 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 ["NCF1 gene sequence", "Copy Number Variations (CNV) in NCF1 gene"] Parameters [] Preparation ["No specific fasting required", "Inform lab of any current medications"] Indications ["Clinical suspicion of Chronic Granulomatous Disease (CGD)", "Family history of CGD", "Recurrent severe infections unresponsive to standard treatment"] Measurement technique Confirm with laboratory Codes LOINC: 94453-4 ICD-10: D71 Clinical summary This test identifies pathogenic variants in the NCF1 gene, confirming a diagnosis of autosomal recessive chronic granulomatous disease type 1.
TEST-5037 NDUFS1 Gene Mitochondrial Complex I Deficiency DNA Test This test identifies pathogenic variants in the NDUFS1 gene, which are associated with mitochondrial complex I deficiency, a severe neurometabolic disorder.	Peripheral Blood (EDTA Whole Blood)	10–12 Business Days	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["NDUFS1 gene sequence", "Single nucleotide variants (SNVs)", "Small insertions/deletions (indels)", "Copy number alterations"] Parameters [] Preparation ["No specific fasting required", "Inform phlebotomist of any medications"] Indications ["Diagnosis of mitochondrial complex I deficiency", "Carrier screening", "Informed family planning", "Familial mutation confirmation"] Measurement technique Confirm with laboratory Codes LOINC: 94222-8 ICD-10: E88.49 Clinical summary This test identifies pathogenic variants in the NDUFS1 gene, which are associated with mitochondrial complex I deficiency, a severe neurometabolic disorder.
TEST-3645 NEK8 Gene Nephronophthisis Type 9 Genetic Test This test analyzes the NEK8 gene to detect pathogenic variants associated with autosomal recessive nephronophthisis type 9.	Peripheral whole blood	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 NEK8 gene", "Single nucleotide variants (SNVs)", "Small insertions/deletions (indels)", "Copy number variations (CNVs)"] Parameters [] Preparation ["No specific patient preparation required."] Indications ["Diagnosis of nephronophthisis type 9", "Carrier testing", "Family screening"] Measurement technique Confirm with laboratory Codes LOINC: 94475-1 ICD-10: Q61.5, Z13.71, Z84.81 Clinical summary This test analyzes the NEK8 gene to detect pathogenic variants associated with autosomal recessive nephronophthisis type 9.
TEST-5318 NOL3 Gene Familial Cortical Myoclonus Genetic Test This test identifies pathogenic variants in the NOL3 gene associated with familial cortical myoclonus using Next-Generation Sequencing (NGS). It detects point mutations, deletions,...	Whole blood (3–5 mL in 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 ["NOL3 gene pathogenic variants", "Deletions/Duplications in NOL3 gene"] Parameters [] Preparation ["Detailed clinical history of myoclonus or epilepsy", "Documented family pedigree"] Indications ["Suspected familial cortical myoclonus", "Family history of myoclonus or epilepsy"] Measurement technique Confirm with laboratory Codes LOINC: 21631-7 ICD-10: G25.3 Clinical summary This test identifies pathogenic variants in the NOL3 gene associated with familial cortical myoclonus using Next-Generation Sequencing (NGS). It detects point mutations, deletions, and duplications.
TEST-5971 NPC1 Gene Niemann-Pick Disease Type C1 Genetic Test This genetic test identifies pathogenic variants in the NPC1 gene associated with Niemann-Pick disease type C1.	Peripheral whole blood, extracted DNA, 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 ["Pathogenic variants in the NPC1 gene"] Parameters [] Preparation ["No specific fasting required", "Inform lab of any relevant medications"] Indications ["Suspected Niemann-Pick disease type C1 based on clinical presentation", "Family history of NPC1", "Carrier screening in high-risk families"] Measurement technique Confirm with laboratory Codes LOINC: 94070-5 ICD-10: E75.242 Clinical summary This genetic test identifies pathogenic variants in the NPC1 gene associated with Niemann-Pick disease type C1.
TEST-3097 NPR2 Gene Acromesomelic Dysplasia, Maroteaux Type Genetic Test (NGS) This test identifies pathogenic variants in the NPR2 gene associated with Acromesomelic dysplasia, Maroteaux type.	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 NPR2 gene"] Parameters [] Preparation ["Mandatory genetic counselling session", "Family pedigree chart review", "Detailed clinical history provision", "Pre-test counselling call participation"] Indications ["Clinical suspicion of Acromesomelic dysplasia, Maroteaux type", "Evaluation of disproportionate short stature"] Measurement technique Confirm with laboratory Codes LOINC: 81309-1 ICD-10: Q77.8 Clinical summary This test identifies pathogenic variants in the NPR2 gene associated with Acromesomelic dysplasia, Maroteaux type.
TEST-2282 NSD1 Gene Sequencing Test for Sotos Syndrome Type 1 This test detects pathogenic and likely pathogenic variants in the NSD1 gene, which are associated with Sotos syndrome type 1.	Whole Blood (EDTA), Extracted Genomic DNA, or 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 NSD1 gene", "Single-nucleotide variants", "Small insertions or deletions"] Parameters [] Preparation ["No special dietary restrictions", "No medication adjustments required", "No fasting required"] Indications ["Suspected Sotos syndrome type 1 based on clinical features", "Family history of Sotos syndrome type 1", "Genetic counselling for at-risk family members"] Measurement technique Confirm with laboratory Codes LOINC: 90529-3 ICD-10: Q87.3 Clinical summary This test detects pathogenic and likely pathogenic variants in the NSD1 gene, which are associated with Sotos syndrome type 1.
TEST-4881 NXF5 Gene Genetic Test for Non-Syndromic Intellectual Disability This test identifies pathogenic variants in the NXF5 gene, confirming a genetic basis for non-syndromic intellectual disability.	Peripheral Whole Blood or FTA Card	3–4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["NXF5 gene sequence", "Pathogenic variants in coding exons and flanking intronic regions"] Parameters [] Preparation ["No fasting required", "No medication adjustment required"] Indications ["Patients with unexplained intellectual disability", "Patients with developmental delay", "Patients with a family history suggestive of X-linked inheritance"] Measurement technique Confirm with laboratory Codes LOINC: 81247-9 ICD-10: F79 Clinical summary This test identifies pathogenic variants in the NXF5 gene, confirming a genetic basis for non-syndromic intellectual disability.

Category overview

Single Gene: overview

When clinical symptoms or family history point directly toward a specific inherited condition, highly focused genetic testing provides the exact, rapid insights necessary for peace of mind. Integrated into our advanced Molecular Genetics services, Single Gene testing meticulously analyzes one specific gene for known disease-causing mutations. Utilizing cutting-edge diagnostic technology, this highly focused molecular screening helps confirm or rule out precise genetic traits, safely guiding targeted medical interventions and family planning strategies. Recognized for specialized diagnostic excellence among diagnostic labs in the UAE, DNA Labs ensures absolute patient confidentiality, exceptional analytical precision, and incredibly efficient turnaround times. Take an informed step forward in your health journey—schedule your single gene testing in UAE, book a secure home sample collection, or reach out to our expert medical professionals.

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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.