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 256–270 of 297 matching tests.

Single Gene Sequencing diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-6339 SPINT2 Gene Sequencing Test This test evaluates the SPINT2 gene for pathogenic variants associated with congenital sodium diarrhea, syndromic type 3.	Whole 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 ["Pathogenic variants in the SPINT2 gene", "Full coding exons + splice junctions"] Parameters [] Preparation ["No specific fasting required", "Inform lab of any current medications"] Indications ["Diagnosis of congenital sodium diarrhea, syndromic type 3", "Carrier screening", "Guided family planning"] Measurement technique Confirm with laboratory Codes LOINC: 81308-0 ICD-10: P78.3 Clinical summary This test evaluates the SPINT2 gene for pathogenic variants associated with congenital sodium diarrhea, syndromic type 3.
TEST-4844 SPRED1 Gene Legius Syndrome Genetic Test This test evaluates the SPRED1 gene for pathogenic variants associated with Legius syndrome.	Whole Blood (Peripheral)	3 to 4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["SPRED1 gene sequence", "Copy number variants in SPRED1"] Parameters [] Preparation ["No dietary or fasting preparation required", "Inform phlebotomist of current medications, supplements, or bleeding disorders"] Indications ["Clinical suspicion of Legius syndrome", "Differentiation from Neurofibromatosis Type 1 (NF1)"] Measurement technique Confirm with laboratory Codes LOINC: 82939-0 ICD-10: Q85.09 Clinical summary This test evaluates the SPRED1 gene for pathogenic variants associated with Legius syndrome.
TEST-3189 STIM1 Gene (Stormorken Syndrome) Genetic Test This test evaluates the STIM1 gene for pathogenic variants associated with Stormorken syndrome, an autosomal dominant disorder.	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 ["STIM1 gene sequence", "Pathogenic variants"] Parameters [] Preparation [] Indications ["Suspected Stormorken syndrome", "Family history of Stormorken syndrome"] Measurement technique Confirm with laboratory Codes LOINC: 61693-7 ICD-10: D69.1 Clinical summary This test evaluates the STIM1 gene for pathogenic variants associated with Stormorken syndrome, an autosomal dominant disorder.
TEST-4357 SYNE1 Gene Sequencing Test This test identifies pathogenic variants in the SYNE1 gene, confirming a diagnosis of Emery-Dreifuss Muscular Dystrophy Type 4 (EDMD4).	Peripheral whole blood (EDTA tube)	3–4 weeks including pre-test genetic counselling session	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the SYNE1 gene", "Coverage of all coding exons and splice sites"] Parameters [] Preparation ["No fasting is required.", "Provide a detailed neurological and cardiac history.", "Attendance at the mandatory pre-test genetic counselling session is required."] Indications ["Individuals presenting with early joint contractures", "Individuals with progressive muscle wasting", "Individuals with elevated creatine kinase levels", "Individuals with a family history suggestive of EDMD inheritance"] Measurement technique Confirm with laboratory Codes LOINC: 21636-6 ICD-10: G71.0 Clinical summary This test identifies pathogenic variants in the SYNE1 gene, confirming a diagnosis of Emery-Dreifuss Muscular Dystrophy Type 4 (EDMD4).
TEST-4416 TAZ Gene Barth Syndrome Genetic Test This test evaluates the entire coding region and flanking intronic sequences of the TAZ gene using Next-Generation Sequencing (NGS). It detects pathogenic variants associated with...	Peripheral whole blood (EDTA) 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 ["TAZ gene sequence", "Copy number variations in TAZ gene", "Pathogenic variants (point mutations, insertions, deletions)"] Parameters [] Preparation ["No specific fasting required", "Continue all prescribed medications unless advised otherwise by your physician"] Indications ["Suspected Barth syndrome based on clinical presentation", "Family history of Barth syndrome", "Need for definitive genetic diagnosis for management and counseling"] Measurement technique Confirm with laboratory Codes LOINC: 83276-0 ICD-10: E88.8 Clinical summary This test evaluates the entire coding region and flanking intronic sequences of the TAZ gene using Next-Generation Sequencing (NGS). It detects pathogenic variants associated with Barth syndrome.
TEST-2869 TBC1D24 Gene DOOR Syndrome Genetic Test This test identifies pathogenic variants in the TBC1D24 gene associated with DOOR syndrome.	Peripheral Whole Blood, Dried Blood Spot (FTA Card), or Pre-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 TBC1D24 gene", "Full gene coverage"] Parameters [] Preparation ["Pre-test genetic counseling is mandatory"] Indications ["Individuals with clinical features suggestive of DOOR syndrome", "Family members of individuals with DOOR syndrome"] Measurement technique Confirm with laboratory Codes LOINC: 21636-6 ICD-10: Q87.8 Clinical summary This test identifies pathogenic variants in the TBC1D24 gene associated with DOOR syndrome.
TEST-2939 TBX15 Gene Cousin Syndrome Genetic Test This genetic test detects pathogenic and likely pathogenic variants in the T-box 15 gene associated with Cousin syndrome.	Peripheral Whole Blood / DNA (FTA Card acceptable)	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 TBX15 gene", "Single nucleotide variants", "Small insertions and deletions", "Copy number alterations"] Parameters [] Preparation ["No fasting or dietary restrictions are needed"] Indications ["Clinical suspicion of Cousin syndrome", "Family history of Cousin syndrome", "Need for definitive molecular diagnosis"] Measurement technique Confirm with laboratory Codes LOINC: 55221-3 ICD-10: Q87.8 Clinical summary This genetic test detects pathogenic and likely pathogenic variants in the T-box 15 gene associated with Cousin syndrome.
TEST-2279 TBX6 Gene Spondylocostal Dysostosis Type 5 Genetic Test This test identifies pathogenic variants or copy number variations in the TBX6 gene associated with Spondylocostal Dysostosis Type 5.	Whole blood (3–5 mL in EDTA), extracted DNA (1–2 µg), 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 ["TBX6 gene sequence", "Copy Number Variations (CNV) in TBX6"] Parameters [] Preparation ["Pre-test genetic counseling session is mandatory", "Obtain written informed consent"] Indications ["Clinical or radiological features of spondylocostal dysostosis", "Establish a definitive molecular diagnosis", "Guide family counseling"] Measurement technique Confirm with laboratory Codes LOINC: 81205-9 ICD-10: Q76.4 Clinical summary This test identifies pathogenic variants or copy number variations in the TBX6 gene associated with Spondylocostal Dysostosis Type 5.
TEST-4698 TCIRG1 Gene Osteopetrosis Autosomal Recessive Type 1 Genetic Test This diagnostic test evaluates the TCIRG1 gene for pathogenic variants associated with autosomal recessive osteopetrosis type 1.	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 ["Pathogenic variants in the TCIRG1 gene"] Parameters [] Preparation [] Indications ["Confirmation of clinical suspicion of ARO1", "Carrier screening", "Prenatal diagnosis"] Measurement technique Confirm with laboratory Codes LOINC: 88857-4 ICD-10: Q78.2 Clinical summary This diagnostic test evaluates the TCIRG1 gene for pathogenic variants associated with autosomal recessive osteopetrosis type 1.
TEST-2232 TCOF1 Gene (Treacher Collins Syndrome Type 1) Genetic Test This genetic test evaluates the TCOF1 gene for pathogenic variants associated with Treacher Collins syndrome type 1.	Peripheral blood 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 TCOF1 gene", "Entire coding region and splice sites"] Parameters [] Preparation ["No fasting required", "Prior genetic counseling session to document family pedigree is mandatory", "Pre-clinical history documentation"] Indications ["Confirmation of Treacher Collins syndrome type 1 diagnosis", "Guiding surgical planning", "Recurrence risk assessment"] Measurement technique Confirm with laboratory Codes LOINC: 21647-4 ICD-10: Q75.4 Clinical summary This genetic test evaluates the TCOF1 gene for pathogenic variants associated with Treacher Collins syndrome type 1.
TEST-2477 TCTN3 Gene Sequencing for Orofaciodigital Syndrome Type 4 Test This test detects pathogenic variants in the TCTN3 gene associated with Orofaciodigital Syndrome Type 4.	Whole Blood 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 ["Pathogenic variants in TCTN3 gene", "Single-nucleotide variants", "Small insertions", "Small deletions"] Parameters [] Preparation ["No special preparation required", "No fasting required"] Indications ["Clinical suspicion of Orofaciodigital Syndrome Type 4"] Measurement technique Confirm with laboratory Codes LOINC: 21636-6 ICD-10: Q87.0 Clinical summary This test detects pathogenic variants in the TCTN3 gene associated with Orofaciodigital Syndrome Type 4.
TEST-3035 TFAP2A Gene Branchiooculofacial Syndrome Genetic Test This test identifies mutations in the TFAP2A gene associated with Branchiooculofacial syndrome.	Whole blood (EDTA tube), buccal swab, 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 ["Mutations in the TFAP2A gene", "Point mutations", "Small indels", "Copy Number Variations (CNVs)"] Parameters [] Preparation ["No dietary or medication restrictions", "Provide complete clinical history and previous genetic reports"] Indications ["Suspected Branchiooculofacial syndrome", "Family history of BOFS", "Carrier screening", "Prenatal diagnosis"] Measurement technique Confirm with laboratory Codes LOINC: 21624-1 ICD-10: Q87.0 Clinical summary This test identifies mutations in the TFAP2A gene associated with Branchiooculofacial syndrome.
TEST-5686 TFG Gene (SPG57) Genetic Test This test detects pathogenic variants in the TFG gene associated with autosomal recessive hereditary spastic paraplegia type 57 (SPG57).	Peripheral 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 TFG gene"] Parameters [] Preparation ["No fasting required", "No medication changes required"] Indications ["Confirmation of clinical diagnosis of SPG57", "Family planning for individuals with SPG57", "Differential diagnosis of neurological disorders"] Measurement technique Confirm with laboratory Codes LOINC: 91518-1 ICD-10: G11.4 Clinical summary This test detects pathogenic variants in the TFG gene associated with autosomal recessive hereditary spastic paraplegia type 57 (SPG57).
TEST-4834 TGFBR1 Gene Loeys-Dietz Syndrome Type 2A Genetic Test (NGS) This molecular diagnostic test identifies pathogenic variants in the TGFBR1 gene, which are causative for Loeys-Dietz syndrome type 2A.	Peripheral whole blood (3–5 mL in EDTA tube) 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 TGFBR1 gene coding region"] Parameters [] Preparation ["Prior genetic counselling required", "Detailed three-generation pedigree chart required", "Written informed consent required"] Indications ["Clinical suspicion of Loeys-Dietz syndrome type 2A", "Family history of Loeys-Dietz syndrome"] Measurement technique Confirm with laboratory Codes LOINC: 82994-1 ICD-10: Q87.89, Q87.8 Clinical summary This molecular diagnostic test identifies pathogenic variants in the TGFBR1 gene, which are causative for Loeys-Dietz syndrome type 2A.
TEST-5221 TIMM21 Gene Mitochondrial Respiratory Chain Disease, TIMM21-Related Genetic Test This test identifies pathogenic variants within the TIMM21 gene associated with mitochondrial respiratory chain disorders.	Whole Blood (EDTA), Dried Blood Spot (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 TIMM21 gene", "Single-nucleotide variants (SNVs)", "Insertions/Deletions (Indels)", "Gene deletions/duplications"] Parameters [] Preparation ["Pre-test genetic counseling is mandatory", "Referral from Neurologist, Medical Geneticist, or Pulmonologist is required"] Indications ["Clinical suspicion of mitochondrial respiratory chain disease", "Progressive neurological decline", "Inconclusive biochemical assays"] Measurement technique Confirm with laboratory Codes LOINC: 104204-1 ICD-10: E88.49 Clinical summary This test identifies pathogenic variants within the TIMM21 gene associated with mitochondrial respiratory chain disorders.

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.