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

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Single Gene Sequencing test prices

Showing 271–285 of 297 matching tests.

Single Gene Sequencing diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-6205 TJP2 Gene Hypercholanemia Genetic Test This genetic test identifies pathogenic variants in the TJP2 gene associated with progressive familial intrahepatic cholestasis type 4 (PFIC4). It helps confirm the diagnosis in pa...	Peripheral whole blood (EDTA) or buccal swab	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 TJP2 gene", "Bile acid transport defects"] Parameters [] Preparation ["Simple genetic counseling session", "No fasting required", "No medication changes needed"] Indications ["Confirmation of PFIC4 diagnosis", "Evaluation of unexplained cholestasis", "Assessment of liver disease progression"] Measurement technique Confirm with laboratory Codes LOINC: 81247-9 ICD-10: K76.8 Clinical summary This genetic test identifies pathogenic variants in the TJP2 gene associated with progressive familial intrahepatic cholestasis type 4 (PFIC4). It helps confirm the diagnosis in patients presenting with symptoms of cholestasis and liver disease.
TEST-4112 TMCO1 Gene Craniofacial Dysmorphism, Skeletal Anomalies & Mental Retardation Syndrome NGS Test This diagnostic test evaluates the TMCO1 gene for pathogenic variants linked to craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome.	Whole Blood (EDTA), FTA Card Blood Spot, or Extracted DNA	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["TMCO1 gene coding region variants", "Pathogenic mutations"] Parameters [] Preparation ["Attend a pre-test genetic counseling session", "Provide detailed family history"] Indications ["Diagnosis of TMCO1-related syndrome", "Genetic counseling", "Management planning"] Measurement technique Confirm with laboratory Codes LOINC: 102502-1 ICD-10: Q87.8 Clinical summary This diagnostic test evaluates the TMCO1 gene for pathogenic variants linked to craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome.
TEST-4584 TMEM231 Gene Joubert Syndrome Type 20 Genetic Test This genetic test identifies pathogenic variants in the TMEM231 gene associated with Joubert syndrome type 20.	Whole blood (3 mL) or saliva	3–4 Weeks (express reporting available)	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in TMEM231 gene", "Copy number variations (deletions/duplications) in TMEM231 gene"] Parameters [] Preparation ["Mandatory genetic counselling session prior to sample collection", "Provide a three-generation family pedigree"] Indications ["Suspected Joubert syndrome type 20", "Neurodevelopmental disorder with characteristic MRI findings"] Measurement technique Confirm with laboratory Codes LOINC: 101356-6 ICD-10: Q04.3 Clinical summary This genetic test identifies pathogenic variants in the TMEM231 gene associated with Joubert syndrome type 20.
TEST-4653 TNFRSF11B Gene (Paget Disease, Juvenile) Genetic Test This test evaluates the TNFRSF11B gene for mutations associated with juvenile Paget disease (hereditary hyperphosphatasia).	Peripheral whole blood, 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 ["Full coding sequence of the TNFRSF11B gene", "Single nucleotide variants (SNVs)", "Insertions/Deletions (Indels)"] Parameters [] Preparation ["No specific fasting required", "No medication adjustments needed unless advised by physician"] Indications ["Suspected juvenile Paget disease based on clinical presentation", "Family history of juvenile Paget disease", "Need for definitive molecular diagnosis"] Measurement technique Confirm with laboratory Codes LOINC: 81247-9 ICD-10: M88.89 Clinical summary This test evaluates the TNFRSF11B gene for mutations associated with juvenile Paget disease (hereditary hyperphosphatasia).
TEST-5496 TSEN54 Gene Pontocerebellar Hypoplasia Type 2A Genetic Test This diagnostic test evaluates the TSEN54 gene for pathogenic variants associated with Pontocerebellar Hypoplasia Type 2A.	Whole Blood (3-5 mL EDTA) or Saliva (Oragene DNA Kit)	14–21 calendar days	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the TSEN54 gene", "Single nucleotide variants", "Small insertions/deletions", "Cryptic splice mutations"] Parameters [] Preparation ["No specific fasting required", "Inform lab of any medications"] Indications ["Suspected Pontocerebellar Hypoplasia Type 2A", "Family history of PCH2A", "Neurodevelopmental disorder with cerebellar hypoplasia"] Measurement technique Confirm with laboratory Codes LOINC: 76006-3 ICD-10: Q04.8 Clinical summary This diagnostic test evaluates the TSEN54 gene for pathogenic variants associated with Pontocerebellar Hypoplasia Type 2A.
TEST-2305 TTC21B Genetic Test (Short-Rib Thoracic Dysplasia Type 4) This test identifies pathogenic mutations in the TTC21B gene associated with short-rib thoracic dysplasia type 4.	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 ["TTC21B gene mutations", "Copy Number Variations (CNVs) in TTC21B"] Parameters [] Preparation ["Fasting is not required", "Stay hydrated", "Inform phlebotomist of bleeding disorders or medications"] Indications ["Suspected diagnosis of Short-Rib Thoracic Dysplasia Type 4", "Family history of TTC21B-related disorders", "Genetic counseling for recurrence risk assessment"] Measurement technique Confirm with laboratory Codes LOINC: 55233-1 ICD-10: Q77.2 Clinical summary This test identifies pathogenic mutations in the TTC21B gene associated with short-rib thoracic dysplasia type 4.
TEST-2437 TUBB2B Gene Polymicrogyria Asymmetric Genetic Test This test detects pathogenic variants in the TUBB2B gene associated with asymmetric polymicrogyria.	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 TUBB2B gene", "Single nucleotide variants", "Indels", "Copy number changes"] Parameters [] Preparation [] Indications ["Suspected diagnosis of asymmetric polymicrogyria", "Family history of TUBB2B-related disorders", "Genetic counseling for recurrence risk assessment"] Measurement technique Confirm with laboratory Codes LOINC: 21636-6 ICD-10: Q04.3 Clinical summary This test detects pathogenic variants in the TUBB2B gene associated with asymmetric polymicrogyria.
TEST-3626 TUBB3 Gene Sequencing for CFEOM3A Test This test detects pathogenic variants in the TUBB3 gene, which are associated with congenital fibrosis of extraocular muscles type 3A (CFEOM3A).	Whole Blood (Peripheral)	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 TUBB3 gene"] Parameters [] Preparation ["No specific fasting required", "Do not discontinue prescribed medications"] Indications ["Suspected diagnosis of CFEOM3A", "Family history of CFEOM3A", "Genetic counselling for families with CFEOM3A"] Measurement technique Confirm with laboratory Codes LOINC: 59110-7 ICD-10: H49.81 Clinical summary This test detects pathogenic variants in the TUBB3 gene, which are associated with congenital fibrosis of extraocular muscles type 3A (CFEOM3A).
TEST-4682 TUBB4A Gene Leukodystrophy Hypomyelinating Type 6 Genetic Test This test identifies disease-causing mutations in the TUBB4A gene to confirm a molecular diagnosis of hypomyelinating leukodystrophy type 6.	Peripheral Whole Blood (3–5 mL in EDTA) or Buccal Swab	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 ["Pathogenic variants in the TUBB4A gene"] Parameters [] Preparation ["Ensure child is well hydrated", "Topical anaesthetic cream may be applied if prescribed"] Indications ["Suspected hypomyelinating leukodystrophy type 6", "Family history of TUBB4A-related disorders"] Measurement technique Confirm with laboratory Codes LOINC: 21665-1 ICD-10: E75.23 Clinical summary This test identifies disease-causing mutations in the TUBB4A gene to confirm a molecular diagnosis of hypomyelinating leukodystrophy type 6.
TEST-5342 TUBG1 Gene Neurodevelopmental Malformation and Microcephaly Genetic Test This test identifies pathogenic variants in the TUBG1 gene, which are associated with autosomal dominant microcephaly and cortical brain malformations.	Peripheral Whole Blood (Venipuncture) 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 TUBG1 gene", "Point mutations", "Small insertions and deletions", "Copy number variations"] Parameters [] Preparation [] Indications ["Infants and children with congenital microcephaly", "Individuals with cortical brain malformations", "Patients with global developmental delay", "Adults seeking molecular diagnosis for family planning"] Measurement technique Confirm with laboratory Codes LOINC: 101389-3 ICD-10: Q02, F79, Z13.79 Clinical summary This test identifies pathogenic variants in the TUBG1 gene, which are associated with autosomal dominant microcephaly and cortical brain malformations.
TEST-5218 TYMP Gene MNGIE Syndrome (Without Leukoencephalopathy) Genetic Test This genetic test identifies mutations in the TYMP gene associated with MNGIE syndrome without leukoencephalopathy.	Whole Blood (EDTA tube), 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 ["Mutations in the TYMP gene", "Full TYMP gene sequencing (all exons & splice sites)"] Parameters [] Preparation ["No fasting required", "No medication adjustment required", "Carry relevant medical reports and previous neurological investigations"] Indications ["Suspected MNGIE syndrome", "Family history of MNGIE syndrome"] Measurement technique Confirm with laboratory Codes LOINC: 81305-3 ICD-10: E88.49 Clinical summary This genetic test identifies mutations in the TYMP gene associated with MNGIE syndrome without leukoencephalopathy.
TEST-3473 TYRP1 Oculocutaneous Albinism Type 3 (OCA3) Genetic Test This genetic test evaluates the TYRP1 gene for pathogenic variants associated with oculocutaneous albinism type 3 (OCA3). It helps confirm the diagnosis in individuals with suspect...	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 TYRP1 gene"] Parameters [] Preparation [] Indications ["Individuals presenting with fair skin, light hair, nystagmus, reduced visual acuity", "Family history suggestive of autosomal recessive albinism"] Measurement technique Confirm with laboratory Codes LOINC: 21636-6 ICD-10: E70.32 Clinical summary This genetic test evaluates the TYRP1 gene for pathogenic variants associated with oculocutaneous albinism type 3 (OCA3). It helps confirm the diagnosis in individuals with suspected OCA3.
TEST-3780 UMOD Gene Hyperuricemic Nephropathy, Familial Juvenile Type 1 Genetic Test This genetic test analyzes the UMOD gene for mutations associated with familial juvenile hyperuricemic nephropathy type 1.	Peripheral whole blood (EDTA), 2–5 mL; also accepted: extracted genomic DNA, FTA card spots	21–28 calendar days	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["UMOD gene variants", "Pathogenic and likely-pathogenic variants"] Parameters [] Preparation ["No fasting required", "Inform team of recent blood transfusions, bone marrow transplants, or active malignancies"] Indications ["Suspected familial juvenile hyperuricemic nephropathy type 1", "Family history of early-onset kidney disease or gout", "Need for cascade screening in at-risk relatives"] Measurement technique Confirm with laboratory Codes LOINC: 94487-1 ICD-10: N11.0 Clinical summary This genetic test analyzes the UMOD gene for mutations associated with familial juvenile hyperuricemic nephropathy type 1.
TEST-3062 UPB1 Gene Beta-Ureidopropionase Deficiency Genetic Test This genetic test evaluates the UPB1 gene for mutations associated with beta-ureidopropionase deficiency.	Peripheral Blood, Extracted DNA, or FTA Card Dried Blood Spot	3–4 Weeks (21–28 Business Days)	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["UPB1 gene sequence", "Single nucleotide variants", "Insertions/deletions", "Copy number variations"] Parameters [] Preparation [] Indications ["Infants, children, or adults presenting with symptoms suggestive of a pyrimidine disorder", "Carrier screening in families with a known UPB1 mutation", "At-risk relatives seeking clarity"] Measurement technique Confirm with laboratory Codes LOINC: 21636-6 ICD-10: E79.8 Clinical summary This genetic test evaluates the UPB1 gene for mutations associated with beta-ureidopropionase deficiency.
TEST-5933 UROS Gene Congenital Erythropoietic Porphyria (CEP) Genetic Test This genetic test analyzes the UROS gene for pathogenic variants associated with Congenital Erythropoietic Porphyria (CEP). It identifies mutations causing this rare metabolic diso...	Peripheral Whole Blood or FTA Card (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 UROS gene", "SNVs, indels, CNVs"] Parameters [] Preparation ["No specific fasting required", "Do not discontinue prescribed medication without consulting your doctor"] Indications ["Clinical suspicion of Congenital Erythropoietic Porphyria (CEP)", "Positive family history of CEP", "Severe photosensitivity presenting in infancy", "Hemolytic anemia with photosensitivity"] Measurement technique Confirm with laboratory Codes LOINC: 21671-7 ICD-10: E80.0 Clinical summary This genetic test analyzes the UROS gene for pathogenic variants associated with Congenital Erythropoietic Porphyria (CEP). It identifies mutations causing this rare metabolic disorder characterized by photosensitivity and hemolytic anemia.

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.