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 121–135 of 297 matching tests.

Single Gene Sequencing diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-3938 GPR101 Gene Test This genetic test evaluates the GPR101 gene for mutations associated with X-linked acrogigantism and early-onset acromegaly.	Whole Blood (EDTA), Extracted DNA (TE buffer), or One Drop Blood on FTA Card	3-4 Weeks (expedited options available)	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the GPR101 gene", "Germline mutations"] Parameters [] Preparation ["Ensure a formal genetic counselling session is completed before sample submission.", "Provide a pedigree chart if available."] Indications ["Diagnosis of X-linked acrogigantism (X-LAG)", "Assessment of familial risk for acromegaly", "Identification of individuals at high risk for pituitary adenomas"] Measurement technique Confirm with laboratory Codes LOINC: 92735-7 ICD-10: Z15.89 Clinical summary This genetic test evaluates the GPR101 gene for mutations associated with X-linked acrogigantism and early-onset acromegaly.
TEST-2960 GPSM2 Gene (Chudley-McCullough Syndrome) Genetic Test This test evaluates the GPSM2 gene for pathogenic variants associated with Chudley-McCullough 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 ["GPSM2 gene sequence", "Pathogenic variants in GPSM2"] Parameters [] Preparation ["No fasting required", "Genetic counseling session mandatory", "Pedigree documentation mandatory"] Indications ["Suspected Chudley-McCullough syndrome", "Family history of Chudley-McCullough syndrome", "Evaluation of sensorineural hearing loss and developmental delay"] Measurement technique Confirm with laboratory Codes LOINC: 55233-1 ICD-10: Q87.8 Clinical summary This test evaluates the GPSM2 gene for pathogenic variants associated with Chudley-McCullough syndrome.
TEST-4333 GRIN2D Gene Early Infantile Epileptic Encephalopathy Type 46 Genetic Test This genetic test analyzes the GRIN2D gene to detect mutations associated with Early Infantile Epileptic Encephalopathy Type 46.	Peripheral whole blood, extracted DNA, or DNA FTA card	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["GRIN2D gene mutations", "Single nucleotide variants (SNVs)", "Small insertions/deletions (indels)", "Copy number variations (CNVs)"] Parameters [{"name": "Analytical Sensitivity", "reference_range": "99.9%"}, {"name": "Analytical Specificity", "reference_range": "99.9%"}, {"name": "Methodology", "reference_range": "Next Generation Sequencing (NGS)"}] Preparation ["No specific fasting required", "Continue all prescribed medications unless advised otherwise by your doctor"] Indications ["Infants and children exhibiting drug-resistant seizures", "Developmental regression", "Abnormal EEG patterns within the first months of life", "Clinical diagnosis or family history of epileptic encephalopathy"] Measurement technique Confirm with laboratory Codes LOINC: 21646-2 ICD-10: G40.4 Clinical summary This genetic test analyzes the GRIN2D gene to detect mutations associated with Early Infantile Epileptic Encephalopathy Type 46.
TEST-4497 GTF2H5 Gene Trichothiodystrophy Genetic Test This test identifies pathogenic variants in the GTF2H5 gene, confirming a diagnosis of trichothiodystrophy.	Peripheral Whole Blood, Extracted DNA, or Dried Blood Spot (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 GTF2H5 gene"] Parameters [] Preparation [] Indications ["Individuals with symptoms suggestive of trichothiodystrophy", "Family history of trichothiodystrophy", "Diagnostic confirmation", "Family planning"] Measurement technique Confirm with laboratory Codes LOINC: 48808-6 ICD-10: Q84.1 Clinical summary This test identifies pathogenic variants in the GTF2H5 gene, confirming a diagnosis of trichothiodystrophy.
TEST-3565 GUCA1A Gene Cone-Rod Dystrophy Type 14 NGS Test This test identifies pathogenic variants in the GUCA1A gene associated with cone-rod dystrophy type 14.	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 GUCA1A gene"] Parameters [] Preparation [] Indications ["Clinical suspicion of cone-rod dystrophy type 14", "Family history of inherited retinal disorders"] Measurement technique Confirm with laboratory Codes LOINC: 100347-5 ICD-10: H35.54 Clinical summary This test identifies pathogenic variants in the GUCA1A gene associated with cone-rod dystrophy type 14.
TEST-4804 GUCY2C Gene Sequencing for Meconium Ileus Genetic Test This test evaluates the GUCY2C gene for pathogenic variants associated with meconium ileus and familial diarrhea.	Whole Blood (EDTA Tube) or Dried Blood Spot (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 GUCY2C gene", "Single nucleotide variants", "Small indels", "Copy number variations (CNV)"] Parameters [] Preparation ["No specific fasting required", "Do not discontinue prescribed medication without consulting a doctor"] Indications ["Neonatal meconium ileus without cystic fibrosis", "Familial diarrhea", "Genetic counseling for families with GUCY2C-related disorders"] Measurement technique Confirm with laboratory Codes LOINC: 94219-4 ICD-10: P76.1 Clinical summary This test evaluates the GUCY2C gene for pathogenic variants associated with meconium ileus and familial diarrhea.
TEST-5779 HADHA Gene Sequencing (Trifunctional Protein Deficiency) Test This genetic test evaluates the HADHA gene for pathogenic variants associated with mitochondrial trifunctional protein deficiency.	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 ["HADHA gene coding region", "Pathogenic variants"] Parameters [] Preparation ["No specific fasting required", "Do not modify prescribed medications or dietary regimens without consulting your physician"] Indications ["Suspected mitochondrial trifunctional protein deficiency", "Family screening for HADHA variants", "Metabolic crises"] Measurement technique Confirm with laboratory Codes LOINC: 82267-7 ICD-10: E71.32 Clinical summary This genetic test evaluates the HADHA gene for pathogenic variants associated with mitochondrial trifunctional protein deficiency.
TEST-3200 HAX1 Gene (Severe Congenital Neutropenia Type 3) Genetic Test This genetic test evaluates the HAX1 gene for mutations associated with severe congenital neutropenia type 3 (Kostmann disease). It identifies pathogenic variants responsible for t...	Peripheral Blood (Home Collection via VIP Mobile Phlebotomy or FTA Card)	3–4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["HAX1 gene sequence", "Pathogenic variants (point mutations, indels, CNVs)"] Parameters [] Preparation ["No specific fasting required", "Do not discontinue prescribed medications without consulting physician"] Indications ["Infants with recurrent severe infections and persistent neutropenia", "Family members of confirmed cases", "Suspicious clinical course in adults", "Prior inconclusive work-up"] Measurement technique Confirm with laboratory Codes LOINC: 103000-6 ICD-10: D70.0 Clinical summary This genetic test evaluates the HAX1 gene for mutations associated with severe congenital neutropenia type 3 (Kostmann disease). It identifies pathogenic variants responsible for the condition.
TEST-4865 HEPACAM Gene MLC2A Genetic Test This diagnostic test evaluates the HEPACAM gene for pathogenic variants associated with Megalencephalic Leukoencephalopathy with Subcortical Cysts Type 2A (MLC2A).	Whole Blood (4mL EDTA tube) or FTA Card (infants)	3 to 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 HEPACAM gene", "Variants of Uncertain Significance (VUS) in the HEPACAM gene", "Likely pathogenic variants in the HEPACAM gene"] Parameters [] Preparation ["No specific fasting required", "Inform DNA Labs UAE of any current medications"] Indications ["Individuals with clinical features suggestive of MLC2A", "Asymptomatic siblings of confirmed MLC2A cases", "Carrier screening for at-risk couples with a known family history of MLC2A"] Measurement technique Confirm with laboratory Codes LOINC: 94834-7 ICD-10: G93.8 Clinical summary This diagnostic test evaluates the HEPACAM gene for pathogenic variants associated with Megalencephalic Leukoencephalopathy with Subcortical Cysts Type 2A (MLC2A).
TEST-6023 HNF1B Gene Maturity-Onset Diabetes of the Young Type 5 Genetic Test This test detects pathogenic variants in the HNF1B gene to diagnose Maturity-Onset Diabetes of the Young type 5 (MODY 5).	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 HNF1B gene", "Presence of mutations associated with MODY 5"] Parameters [] Preparation ["No specific fasting required for blood sample collection.", "No medication adjustments needed prior to sample collection."] Indications ["Suspected diagnosis of MODY 5", "Family history suggestive of monogenic diabetes", "Differentiation from Type 1 or Type 2 diabetes"] Measurement technique Confirm with laboratory Codes LOINC: 82939-0 ICD-10: E13.9 Clinical summary This test detects pathogenic variants in the HNF1B gene to diagnose Maturity-Onset Diabetes of the Young type 5 (MODY 5).
TEST-5455 HSPB8 Gene Neuronopathy (Distal Hereditary Motor Neuropathy Type 2A) Genetic Test This test identifies pathogenic variants in the HSPB8 gene associated with Distal Hereditary Motor Neuropathy Type 2A (dHMN2A).	Peripheral whole blood, extracted DNA, or 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 HSPB8 gene"] Parameters [] Preparation ["No specific fasting required", "No medication or diet restrictions"] Indications ["Suspected diagnosis of Distal Hereditary Motor Neuropathy Type 2A (dHMN2A)", "Family history of dHMN2A", "Need for genetic counseling and reproductive planning"] Measurement technique Confirm with laboratory Codes LOINC: 82939-0 ICD-10: G12.21 Clinical summary This test identifies pathogenic variants in the HSPB8 gene associated with Distal Hereditary Motor Neuropathy Type 2A (dHMN2A).
TEST-3015 IARS2 Gene Genetic Test This test identifies pathogenic variants in the IARS2 gene associated with a rare multisystem syndrome.	Whole Blood (EDTA), Saliva, 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 IARS2 gene", "Coding exons", "Splice sites", "Copy number variants (CNVs)"] Parameters [] Preparation ["No specific preparation required."] Indications ["Patients with features suggestive of mitochondrial aminoacyl-tRNA synthetase deficiency", "Confirmatory diagnosis", "Carrier testing", "Family counselling"] Measurement technique Confirm with laboratory Codes LOINC: 81265-5 ICD-10: E88.49, Z13.79 Clinical summary This test identifies pathogenic variants in the IARS2 gene associated with a rare multisystem syndrome.
TEST-6336 IGF2 Gene Diabetes Genetic Test This test evaluates the IGF2 gene for pathogenic variants associated with an increased risk of developing diabetes.	Whole Blood, Extracted DNA, or Dried Blood Spot (FTA Card)	3–4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["IGF2 gene variants", "Pathogenic mutations in coding exons and splice junctions"] Parameters [] Preparation ["No specific fasting required", "No medication or diet adjustments needed"] Indications ["Individuals with a strong family history of early-onset diabetes", "Individuals with unexplained metabolic syndrome features"] Measurement technique Confirm with laboratory Codes LOINC: 10193-4 ICD-10: E11.9, R73.03, Z13.1 Clinical summary This test evaluates the IGF2 gene for pathogenic variants associated with an increased risk of developing diabetes.
TEST-4852 IKBKG Gene Genetic Test This test identifies pathogenic variants in the IKBKG gene associated with primary immunodeficiency syndromes.	Peripheral Whole Blood (EDTA) or Extracted DNA	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["IKBKG gene variants", "Single nucleotide variants", "Small insertions/deletions", "Copy number alterations"] Parameters [] Preparation ["Inform lab of anticoagulant use", "Fasting is not required"] Indications ["Suspected recurrent invasive pneumococcal disease type 2", "Suspected Incontinentia Pigmenti", "Suspected X-linked EDA-ID immunodeficiency"] Measurement technique Confirm with laboratory Codes LOINC: 85800-2 ICD-10: D82.8, Q82.3, B95.3 Clinical summary This test identifies pathogenic variants in the IKBKG gene associated with primary immunodeficiency syndromes.
TEST-5338 IL12RB2 Genetic Testing Test This test identifies mutations in the IL12RB2 gene, which are responsible for Mendelian Susceptibility to Mycobacterial Disease (MSMD).	Whole blood, extracted DNA, or one-drop FTA card	3–4 weeks (expedited 10-day option available)	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Germline mutations in the IL12RB2 gene", "Coverage of all IL12RB2 exons and splice sites"] Parameters [] Preparation ["No fasting required"] Indications ["Suspected Mendelian Susceptibility to Mycobacterial Disease (MSMD)", "Family history of MSMD", "Recurrent severe infections with atypical mycobacteria"] Measurement technique Confirm with laboratory Codes LOINC: 96603-4 ICD-10: D81.3, Z15.09, Z14.8 Clinical summary This test identifies mutations in the IL12RB2 gene, which are responsible for Mendelian Susceptibility to Mycobacterial Disease (MSMD).

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.