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 61–75 of 297 matching tests.

Single Gene Sequencing diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-2439 COL2A1 Gene Platyspondylic Skeletal Dysplasia, Torrance Type Genetic Test This test identifies mutations in the COL2A1 gene, providing a definitive diagnosis for Torrance-type platyspondylic skeletal dysplasia.	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 ["COL2A1 gene mutations (SNVs, Indels, Large Deletions/Duplications)"] Parameters [] Preparation ["No fasting required", "Patient must be afebrile for 24 hours prior"] Indications ["Suspected diagnosis of Torrance-type platyspondylic skeletal dysplasia", "Need to differentiate from other COL2A1 phenotypes"] Measurement technique Confirm with laboratory Codes LOINC: 81247-9 ICD-10: Q77.7 Clinical summary This test identifies mutations in the COL2A1 gene, providing a definitive diagnosis for Torrance-type platyspondylic skeletal dysplasia.
TEST-5506 COLEC11 Gene 3MC Syndrome Type 2 Genetic Test This genetic test identifies pathogenic variants in the COLEC11 gene, confirming a diagnosis of 3MC syndrome type 2.	Blood (whole blood) 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 COLEC11 gene"] Parameters [] Preparation [] Indications ["Suspected 3MC syndrome type 2", "Family history of 3MC syndrome type 2", "Carrier screening"] Measurement technique Confirm with laboratory Codes LOINC: 100430-5 ICD-10: Q87.0, Z14.8, Z83.89 Clinical summary This genetic test identifies pathogenic variants in the COLEC11 gene, confirming a diagnosis of 3MC syndrome type 2.
TEST-6068 COMT Gene Catechol-O-Methyltransferase Deficiency Genetic Test This genetic test evaluates the entire COMT gene for pathogenic variants linked to catechol-O-methyltransferase deficiency.	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 ["COMT gene sequence", "Pathogenic variants in COMT gene"] Parameters [] Preparation ["No specific fasting required", "No medication or diet restrictions"] Indications ["Suspected catechol-O-methyltransferase deficiency", "Personal or family history of related conditions", "Guiding medication selection"] Measurement technique Confirm with laboratory Codes LOINC: 90535-9 ICD-10: E70.8, Z15.8, F79 Clinical summary This genetic test evaluates the entire COMT gene for pathogenic variants linked to catechol-O-methyltransferase deficiency.
TEST-4883 CORO1A Gene (Immunodeficiency Type 8) Genetic Test This test identifies pathogenic variants in the CORO1A gene, confirming a diagnosis of severe combined immunodeficiency type 8.	Peripheral whole blood	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["CORO1A gene sequence", "Pathogenic variants in CORO1A"] Parameters [] Preparation ["Completed clinical history form", "Three-generation pedigree", "Pre-test genetic counseling"] Indications ["Clinical suspicion of inherited immune dysregulation", "Recurrent bacterial or viral skin infections", "Persistent warts", "Family history suggestive of early-onset immune defects"] Measurement technique Confirm with laboratory Codes LOINC: 82266-3 ICD-10: D81.2, D81.8, Z15.89 Clinical summary This test identifies pathogenic variants in the CORO1A gene, confirming a diagnosis of severe combined immunodeficiency type 8.
TEST-3846 COX20 Gene Ataxia and Muscle Hypotonia Genetic Test This test identifies pathogenic variants in the COX20 gene associated with mitochondrial complex IV deficiency, cerebellar ataxia, and muscle hypotonia.	Whole Blood (EDTA), 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 COX20 gene", "Single nucleotide variants", "Small insertions/deletions", "Copy number variants"] Parameters [] Preparation ["No specific fasting required.", "Do not discontinue prescribed medication without consulting your treating physician."] Indications ["Clinical suspicion of mitochondrial disease", "Unexplained cerebellar ataxia", "Congenital hypotonia with elevated lactate"] Measurement technique Confirm with laboratory Codes LOINC: 101398-2 ICD-10: G31.81, G11.1, P94.2 Clinical summary This test identifies pathogenic variants in the COX20 gene associated with mitochondrial complex IV deficiency, cerebellar ataxia, and muscle hypotonia.
TEST-5850 CRB2 Gene Ventriculomegaly with Cystic Kidney Disease Genetic Test This genetic test identifies pathogenic variants in the CRB2 gene associated with ciliopathies affecting brain and kidney development.	Peripheral Whole Blood or Saliva (Oragene DNA Kit)	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 CRB2 gene"] Parameters [] Preparation ["No special preparation like fasting is required", "Pre-test genetic counseling is recommended"] Indications ["Clinical suspicion of CRB2-associated ciliopathy"] Measurement technique Confirm with laboratory Codes LOINC: 101650-8 ICD-10: Q04.8, Q61.9 Clinical summary This genetic test identifies pathogenic variants in the CRB2 gene associated with ciliopathies affecting brain and kidney development.
TEST-1685 Crigler-Najjar Syndrome Single Gene Sequencing Test This test identifies mutations in the UGT1A1 gene, which are the cause of Crigler-Najjar syndrome, a rare inherited disorder affecting bilirubin metabolism.	Whole Blood (peripheral)	7–8 working days	3,600.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["UGT1A1 gene mutations", "Bilirubin metabolism pathway defects"] Parameters [{"name": "UGT1A1 Gene Sequencing", "reference_range": null}] Preparation ["No specific fasting required", "Do not discontinue prescribed medication"] Indications ["Suspected Crigler-Najjar syndrome", "Prenatal diagnosis", "Carrier screening", "Confirmatory testing for jaundice"] Measurement technique Confirm with laboratory Codes LOINC: 21626-6 ICD-10: E80.5 Clinical summary This test identifies mutations in the UGT1A1 gene, which are the cause of Crigler-Najjar syndrome, a rare inherited disorder affecting bilirubin metabolism.
TEST-5417 CROCC Gene Sequencing Test This test detects pathogenic variants in the CROCC gene associated with neurodevelopmental disorders.	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 CROCC gene", "Copy Number Variants (CNV)", "Structural Variants"] Parameters [] Preparation ["No fasting required", "All standard medications may be continued unless advised otherwise by a physician"] Indications ["Suspected genetic aetiology for neurodevelopmental disorders", "Unexplained neurodevelopmental delays"] Measurement technique Confirm with laboratory Codes LOINC: 55233-1 ICD-10: F88, Z13.39 Clinical summary This test detects pathogenic variants in the CROCC gene associated with neurodevelopmental disorders.
TEST-5858 CRPPA Gene (Walker-Warburg Syndrome) Genetic Test This genetic test evaluates the entire coding region of the CRPPA gene for pathogenic variants associated with Walker-Warburg syndrome.	Whole Blood (EDTA), 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 CRPPA gene", "Single nucleotide variants (SNVs)", "Small insertions/deletions (indels)", "Copy number variations (CNVs)"] Parameters [] Preparation ["No fasting is needed."] Indications ["Suspected Walker-Warburg syndrome", "Severe congenital muscular dystrophy with brain and eye anomalies"] Measurement technique Confirm with laboratory Codes LOINC: 21636-6 ICD-10: Q87.8 Clinical summary This genetic test evaluates the entire coding region of the CRPPA gene for pathogenic variants associated with Walker-Warburg syndrome.
TEST-4907 CUL4B Gene Mental Retardation, X‑Linked Type 15 DNA Test This test detects pathogenic variants in the CUL4B gene associated with X-linked intellectual disability type 15.	Peripheral Whole Blood, Extracted Genomic DNA, 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 CUL4B gene", "Coverage of all coding exons and flanking intronic regions"] Parameters [] Preparation ["No specific fasting required", "No medication or diet restrictions"] Indications ["Individuals with clinical features suggestive of X‑linked intellectual disability type 15", "Family history of X‑linked intellectual disability type 15"] Measurement technique Confirm with laboratory Codes LOINC: 21636-6 ICD-10: F78.A1 Clinical summary This test detects pathogenic variants in the CUL4B gene associated with X-linked intellectual disability type 15.
TEST-1894 CYLD Gene Analysis for Spiegler-Brooke Syndrome (NGS) Test This test detects germline mutations in the CYLD gene, which are associated with Spiegler-Brooke syndrome (multiple familial trichoepithelioma). It helps in diagnosing the conditio...	Whole Blood (EDTA), Buccal Swab, or Dried Blood Spot (FTA Card)	21–28 Days	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Germline mutations in the CYLD gene", "Pathogenic variants in coding exons and splice-site regions"] Parameters [] Preparation ["No fasting or dietary restrictions are necessary."] Indications ["Diagnosis of Spiegler-Brooke syndrome", "Risk assessment for skin adnexal neoplasms", "Cascade screening of family members"] Measurement technique Confirm with laboratory Codes LOINC: 83403-4 ICD-10: D23.9 Clinical summary This test detects germline mutations in the CYLD gene, which are associated with Spiegler-Brooke syndrome (multiple familial trichoepithelioma). It helps in diagnosing the condition and assessing risk for related skin tumors.
TEST-2720 DCAF17 Gene Sequencing (Woodhouse-Sakati Syndrome) Genetic Test This genetic test sequences the DCAF17 gene to detect variants associated with Woodhouse-Sakati syndrome.	Whole Blood (EDTA), Buccal Swab, 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 ["DCAF17 gene sequence", "Pathogenic variants in DCAF17"] Parameters [] Preparation ["Pre-test genetic counselling is mandatory", "Provide complete medication list"] Indications ["Suspected Woodhouse-Sakati syndrome", "Family history of Woodhouse-Sakati syndrome"] Measurement technique Confirm with laboratory Codes LOINC: 21600-8 ICD-10: E88.89 Clinical summary This genetic test sequences the DCAF17 gene to detect variants associated with Woodhouse-Sakati syndrome.
TEST-5797 DIAPH3 Gene Auditory Neuropathy (Autosomal Dominant) Genetic Test This test identifies pathogenic variants in the DIAPH3 gene associated with autosomal dominant auditory neuropathy spectrum disorder (ANSD).	Peripheral whole blood (5 mL) or buccal swab	3 to 4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["DIAPH3 gene mutations", "Single nucleotide variants (SNVs)", "Small insertions/deletions (indels)"] Parameters [] Preparation ["No fasting required", "Provide detailed clinical history of hearing loss", "Provide previous audiology reports", "List current medications"] Indications ["Diagnosis of autosomal dominant auditory neuropathy", "Carrier screening in families with known DIAPH3 mutations", "Genetic counselling for affected families"] Measurement technique Confirm with laboratory Codes LOINC: 19239-6 ICD-10: H90.5 Clinical summary This test identifies pathogenic variants in the DIAPH3 gene associated with autosomal dominant auditory neuropathy spectrum disorder (ANSD).
TEST-2453 DIS3L2 Gene Perlman Syndrome Genetic Test This test evaluates the DIS3L2 gene for pathogenic variants associated with Perlman syndrome.	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 ["DIS3L2 gene sequence", "Pathogenic variants"] Parameters [] Preparation [] Indications ["Suspected Perlman syndrome", "Congenital overgrowth disorder", "Wilms tumor surveillance planning"] Measurement technique Confirm with laboratory Codes LOINC: 99534-4 ICD-10: Q87.8 Clinical summary This test evaluates the DIS3L2 gene for pathogenic variants associated with Perlman syndrome.
TEST-2926 DISP1 Gene Craniofacial & Neurodevelopmental Abnormalities Genetic Test This test evaluates the DISP1 gene for pathogenic variants associated with craniofacial malformations and neurodevelopmental delay.	Peripheral whole blood	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Single Nucleotide Variants (SNVs)", "Small Insertions/Deletions (indels)", "Copy Number Variants (CNVs)"] Parameters [] Preparation [] Indications ["Diagnostic confirmation of suspected DISP1-related disorders", "Genetic risk assessment for family members"] Measurement technique Confirm with laboratory Codes LOINC: 76679-8 ICD-10: Q04.2, Q87.0, Z15.89 Clinical summary This test evaluates the DISP1 gene for pathogenic variants associated with craniofacial malformations and neurodevelopmental delay.

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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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.