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 286–297 of 297 matching tests.

Single Gene Sequencing diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-3976 VLDLR Gene: Cerebellar Hypoplasia & Mental Retardation with or Without Quadrupedal Locomotion Test This test analyzes the VLDLR gene for pathogenic variants associated with specific neurodevelopmental disorders.	Whole Blood, Dried Blood Spot (FTA Card), or Extracted DNA	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 VLDLR gene", "Copy Number Variations (CNV) in the VLDLR gene"] Parameters [] Preparation ["No specific fasting required", "Avoid recent blood transfusion ( Indications ["Suspected autosomal recessive cerebellar hypoplasia", "Suspected intellectual disability with relevant clinical features", "Family history of VLDLR-related disorders"] Measurement technique Confirm with laboratory Codes LOINC: 94133-1 ICD-10: G11.8, F78.9, Z15.09 Clinical summary This test analyzes the VLDLR gene for pathogenic variants associated with specific neurodevelopmental disorders.
TEST-2328 WDR34 Gene Sequencing (Short-Rib Thoracic Dysplasia Type 11 ± Polydactyly) Genetic Test This test evaluates the WDR34 gene for mutations associated with Short-Rib Thoracic Dysplasia Type 11 (SRTD11), a rare genetic disorder affecting skeletal development.	Whole Blood (EDTA), 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 ["WDR34 gene mutations", "Single nucleotide variants", "Insertions", "Deletions"] Parameters [] Preparation ["Do not discontinue prescribed medication without consulting your physician", "Inform the collection team if on anticoagulants", "Inform the collection team if received a blood transfusion within the past two weeks"] Indications ["Pediatric diagnosis of SRTD11", "Prenatal diagnosis of SRTD11", "Carrier screening for SRTD11", "Familial variant analysis"] Measurement technique Confirm with laboratory Codes LOINC: 21636-6 ICD-10: Q77.2, Q69.9 Clinical summary This test evaluates the WDR34 gene for mutations associated with Short-Rib Thoracic Dysplasia Type 11 (SRTD11), a rare genetic disorder affecting skeletal development.
TEST-2928 WDR35 Gene (Cranioectodermal Dysplasia Type 2) Genetic Test This genetic test identifies pathogenic variants in the WDR35 gene associated with Cranioectodermal Dysplasia Type 2.	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 WDR35 gene", "Deletion/duplication analysis of the WDR35 gene"] Parameters [] Preparation ["No specific fasting required", "Inform lab if currently receiving heparin therapy"] Indications ["Suspected Cranioectodermal Dysplasia Type 2", "Family history of CED2", "Genetic counseling for recurrence risk"] Measurement technique Confirm with laboratory Codes LOINC: 90369-8 ICD-10: Q87.8 Clinical summary This genetic test identifies pathogenic variants in the WDR35 gene associated with Cranioectodermal Dysplasia Type 2.
TEST-2312 WDR35 Gene Short-Rib Thoracic Dysplasia Type 7 With or Without Polydactyly Genetic Test This genetic test analyzes the WDR35 gene to identify mutations associated with short-rib thoracic dysplasia type 7.	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 ["WDR35 gene coding region", "Single Nucleotide Variants (SNVs)", "Insertions/Deletions (indels)", "Copy Number Variations (CNVs)"] Parameters [] Preparation ["No fasting required", "No medication washout required"] Indications ["Clinical suspicion of short-rib thoracic dysplasia type 7", "Family history of skeletal dysplasia", "Need for definitive diagnosis for genetic counselling"] Measurement technique Confirm with laboratory Codes LOINC: 21665-5 ICD-10: Q77.2 Clinical summary This genetic test analyzes the WDR35 gene to identify mutations associated with short-rib thoracic dysplasia type 7.
TEST-5357 WISP3 Gene Progressive Pseudorheumatoid Arthropathy of Childhood (PPAC) Genetic Test This test analyzes the WISP3 gene to detect variants associated with progressive pseudorheumatoid arthropathy of childhood (PPAC). It confirms the genetic basis of this autosomal r...	Peripheral 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 ["WISP3 gene coding region variants", "Single-nucleotide variants", "Small insertions/deletions"] Parameters [] Preparation ["No fasting required", "No medication adjustment required unless instructed by physician", "Mandatory genetic counselling session before testing"] Indications ["Suspected progressive pseudorheumatoid arthropathy of childhood (PPAC)", "Family history of PPAC", "Evaluation of early-onset non-inflammatory arthropathy"] Measurement technique Confirm with laboratory Codes LOINC: 81267-1 ICD-10: M12.8 Clinical summary This test analyzes the WISP3 gene to detect variants associated with progressive pseudorheumatoid arthropathy of childhood (PPAC). It confirms the genetic basis of this autosomal recessive skeletal dysplasia.
TEST-2190 WRN Gene (Werner Syndrome) Genetic Test This test evaluates the WRN gene for pathogenic variants associated with Werner syndrome, a rare autosomal recessive disorder characterized by premature aging.	Blood, 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 ["WRN gene sequence", "Pathogenic variants in WRN gene"] Parameters [] Preparation [] Indications ["Clinical suspicion of Werner syndrome", "Family history of Werner syndrome", "Carrier screening"] Measurement technique Confirm with laboratory Codes LOINC: 81247-9 ICD-10: E34.8 Clinical summary This test evaluates the WRN gene for pathogenic variants associated with Werner syndrome, a rare autosomal recessive disorder characterized by premature aging.
TEST-4782 ZCCHC12 Gene Non‑Syndromic Intellectual Disability Genetic Test This test evaluates the ZCCHC12 gene for pathogenic variants associated with non-syndromic intellectual disability.	Peripheral Whole Blood (3-5 mL) or Saliva (2 mL)	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 ZCCHC12 gene", "Single-nucleotide variants", "Small insertions/deletions"] Parameters [] Preparation ["No fasting required", "Provide clinical history and family pedigree chart"] Indications ["Diagnosis of non-syndromic intellectual disability", "Genetic confirmation in individuals with developmental delay"] Measurement technique Confirm with laboratory Codes LOINC: 81247-9 ICD-10: F79 Clinical summary This test evaluates the ZCCHC12 gene for pathogenic variants associated with non-syndromic intellectual disability.
TEST-2990 ZEB2 Gene Sequencing (NGS) for Congenital Central Hypoventilation Syndrome Test This test identifies pathogenic variants in the ZEB2 gene, providing a molecular diagnosis for congenital central hypoventilation syndrome (CCHS) and Mowat-Wilson syndrome.	Peripheral whole blood (EDTA tube), buccal swab, or pre-extracted genomic 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 ZEB2 gene", "Single-nucleotide variants", "Small insertions and deletions", "Splice-site alterations"] Parameters [] Preparation [] Indications ["Suspected diagnosis of congenital central hypoventilation syndrome (CCHS)", "Suspected diagnosis of Mowat-Wilson syndrome"] Measurement technique Confirm with laboratory Codes LOINC: 97179-1 ICD-10: G47.35, Q87.89 Clinical summary This test identifies pathogenic variants in the ZEB2 gene, providing a molecular diagnosis for congenital central hypoventilation syndrome (CCHS) and Mowat-Wilson syndrome.
TEST-2908 ZIC1 Gene Craniosynostosis Type 6 Genetic Test This test identifies pathogenic variants in the ZIC1 gene, which are associated with craniosynostosis type 6, a condition characterized by premature fusion of skull sutures.	Whole Blood (EDTA) / Extracted DNA / FTA Card	3 to 4 Weeks from sample receipt	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["ZIC1 gene sequence", "Pathogenic variants in ZIC1"] Parameters [] Preparation ["Comprehensive clinical history required", "Genetic counselling session mandatory", "Disclose all current medications, supplements, and herbal preparations"] Indications ["Suspected craniosynostosis type 6", "Family history of craniosynostosis", "Need for recurrence risk assessment"] Measurement technique Confirm with laboratory Codes LOINC: 81247-9 ICD-10: Q75.0 Clinical summary This test identifies pathogenic variants in the ZIC1 gene, which are associated with craniosynostosis type 6, a condition characterized by premature fusion of skull sutures.
TEST-2793 ZIC3 Gene Heterotaxy Visceral Type 1 Genetic Test This test identifies pathogenic variants in the ZIC3 gene associated with visceral heterotaxy type 1.	Peripheral Whole Blood (EDTA), FTA Card, or Extracted Genomic 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 ZIC3 gene", "Single nucleotide variants (SNVs)", "Insertions and deletions (indels)", "Copy number variants (CNVs)"] Parameters [] Preparation ["No specific patient preparation required"] Indications ["Diagnosis of visceral heterotaxy type 1", "Risk stratification", "Informed reproductive planning"] Measurement technique Confirm with laboratory Codes LOINC: 81265-5 ICD-10: Q89.3 Clinical summary This test identifies pathogenic variants in the ZIC3 gene associated with visceral heterotaxy type 1.
TEST-2163 ZIC5 Gene Sequencing Test (NGS) for Brain Disorders This test identifies pathogenic variants in the ZIC5 gene associated with congenital brain malformations and developmental delays.	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 ZIC5 gene"] Parameters [] Preparation ["No fasting required", "Mandatory pre-test genetic counselling session"] Indications ["Congenital brain malformations", "Developmental delays", "Dysmorphic features"] Measurement technique Confirm with laboratory Codes LOINC: 51966-2 ICD-10: Q04.8 Clinical summary This test identifies pathogenic variants in the ZIC5 gene associated with congenital brain malformations and developmental delays.
TEST-3527 ZNF469 Gene Brittle Cornea Syndrome Genetic Test This test evaluates the ZNF469 gene for pathogenic variants associated with Brittle Cornea Syndrome.	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 ["ZNF469 gene coding regions", "ZNF469 gene splice sites"] Parameters [] Preparation [] Indications ["Diagnosis of Brittle Cornea Syndrome", "Identification of carriers in families with a history of the condition", "Genetic counseling for connective tissue disorders"] Measurement technique Confirm with laboratory Codes LOINC: 98544-9 ICD-10: Q78.8 Clinical summary This test evaluates the ZNF469 gene for pathogenic variants associated with Brittle Cornea Syndrome.

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.