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 106–120 of 297 matching tests.

Single Gene Sequencing diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-2450 FGFR2 Gene Pfeiffer Syndrome Genetic Test This test comprehensively analyzes the FGFR2 gene for pathogenic variants associated with Pfeiffer syndrome.	Peripheral whole blood (3–5 mL EDTA) or FTA card 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 FGFR2 gene", "Single nucleotide variants (SNVs)", "Insertions/deletions (indels)", "Splice-site variants"] Parameters [] Preparation ["No specific fasting required", "No medication or diet restrictions"] Indications ["Suspected Pfeiffer syndrome based on clinical findings", "Family history of Pfeiffer syndrome", "Need for genetic counseling and risk assessment"] Measurement technique Confirm with laboratory Codes LOINC: 83800-5 ICD-10: Q87.0 Clinical summary This test comprehensively analyzes the FGFR2 gene for pathogenic variants associated with Pfeiffer syndrome.
TEST-2824 FH Gene Fumarase Deficiency Genetic Testing Test This diagnostic test evaluates the FH gene for pathogenic variants associated with fumarase deficiency and hereditary leiomyomatosis and renal cell cancer (HLRCC).	Peripheral whole blood (EDTA), DNA FTA card, or extracted DNA (genomic)	3–4 weeks from sample receipt	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the FH gene", "Copy Number Variations (CNVs) in the FH gene"] Parameters [] Preparation ["No special preparation (fasting) is required.", "Mandatory genetic counselling session prior to sample collection."] Indications ["Diagnosis of fumarase deficiency", "Risk assessment for HLRCC", "Family history of fumarase deficiency or HLRCC"] Measurement technique Confirm with laboratory Codes LOINC: 62324-8 ICD-10: E72.29 Clinical summary This diagnostic test evaluates the FH gene for pathogenic variants associated with fumarase deficiency and hereditary leiomyomatosis and renal cell cancer (HLRCC).
TEST-2653 FLNB Gene Larsen Syndrome Genetic Test This diagnostic test evaluates the FLNB gene for pathogenic variants associated with specific skeletal dysplasias.	Peripheral 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 FLNB gene", "Exon and splice-site coverage"] Parameters [] Preparation ["No fasting required", "No medication discontinuation required"] Indications ["Suspected Larsen syndrome", "Suspected atelosteogenesis types I and III", "Suspected spondylocarpotarsal synostosis syndrome", "Family history of related skeletal dysplasias"] Measurement technique Confirm with laboratory Codes LOINC: 93341-5 ICD-10: Q68.8, Z15.89, Z84.89 Clinical summary This diagnostic test evaluates the FLNB gene for pathogenic variants associated with specific skeletal dysplasias.
TEST-3063 FOXC1 Gene Sequencing for Axenfeld-Rieger Syndrome Type 3 (NGS) Test This test evaluates the FOXC1 gene for pathogenic variants associated with Axenfeld-Rieger syndrome type 3.	Peripheral whole blood or extracted DNA (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 FOXC1 gene"] Parameters [] Preparation ["No special preparation required", "Keep child well-hydrated (unless medically discouraged)"] Indications ["Suspected Axenfeld-Rieger syndrome type 3", "Family history of Axenfeld-Rieger syndrome"] Measurement technique Confirm with laboratory Codes LOINC: 21655-8 ICD-10: Q13.81 Clinical summary This test evaluates the FOXC1 gene for pathogenic variants associated with Axenfeld-Rieger syndrome type 3.
TEST-4467 FOXF1 Gene NGS Test for Alveolar Capillary Dysplasia with Misalignment of Pulmonary Veins This test identifies pathogenic variants in the FOXF1 gene associated with Alveolar Capillary Dysplasia with Misalignment of Pulmonary Veins (ACDMPV). It provides a definitive mole...	Whole blood, Extracted DNA, or FTA Card Blood Spot	3 to 4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["FOXF1 gene coding region", "Conserved splice sites"] Parameters [] Preparation [] Indications ["Infants with unexplained persistent pulmonary hypertension refractory to standard therapy", "Siblings of confirmed ACDMPV cases", "Parents planning future pregnancies after a previous diagnosis"] Measurement technique Confirm with laboratory Codes LOINC: 82939-0 ICD-10: Q33.8 Clinical summary This test identifies pathogenic variants in the FOXF1 gene associated with Alveolar Capillary Dysplasia with Misalignment of Pulmonary Veins (ACDMPV). It provides a definitive molecular diagnosis for this severe neonatal lung condition.
TEST-4522 FOXN1 Gene Analysis for T‑Cell Immunodeficiency, Alopecia, and Nail Dystrophy Test This test evaluates the FOXN1 gene for pathogenic variants linked to T-cell immunodeficiency, alopecia, and nail dystrophy.	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 ["Pathogenic variants in the FOXN1 gene"] Parameters [] Preparation ["No specific fasting required", "Inform lab if on any medications"] Indications ["Suspected FOXN1-related disorder", "Family history of immunodeficiency, alopecia, or nail dystrophy", "Evaluation of primary immunodeficiency"] Measurement technique Confirm with laboratory Codes LOINC: 85399-6 ICD-10: D84.9, L65.0, L60.8 Clinical summary This test evaluates the FOXN1 gene for pathogenic variants linked to T-cell immunodeficiency, alopecia, and nail dystrophy.
TEST-2808 FTO Gene NGS Test for Growth Retardation, Developmental Delay, and Facial Dysmorphism This test identifies mutations in the FTO gene associated with a rare syndrome causing growth retardation, developmental delay, and facial dysmorphism.	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 ["FTO gene coding region variants", "Single nucleotide variants", "Small insertions/deletions"] Parameters [] Preparation ["No fasting or dietary restrictions required"] Indications ["Suspected FTO-related syndrome", "Growth retardation", "Developmental delay", "Facial dysmorphism"] Measurement technique Confirm with laboratory Codes LOINC: 65887-0 ICD-10: Q87.8, R62.52, F88 Clinical summary This test identifies mutations in the FTO gene associated with a rare syndrome causing growth retardation, developmental delay, and facial dysmorphism.
TEST-3752 GATA3 Gene Hypoparathyroidism, Sensorineural Deafness, and Renal Dysplasia Genetic Test This genetic test identifies pathogenic variants in the GATA3 gene associated with HDR syndrome.	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 ["GATA3 gene sequence", "Single nucleotide variants", "Small insertions/deletions", "Copy number variations"] Parameters [] Preparation ["No fasting required", "No specific medication or diet restrictions"] Indications ["Clinical suspicion of HDR syndrome", "Family history of HDR syndrome", "Need for genetic confirmation for management and surveillance"] Measurement technique Confirm with laboratory Codes LOINC: 78804-5 ICD-10: Q87.8 Clinical summary This genetic test identifies pathogenic variants in the GATA3 gene associated with HDR syndrome.
TEST-4420 GATA4 Gene Atrioventricular Septal Defect Type 4 Next‑Generation Sequencing (NGS) Genetic Test This genetic test identifies mutations in the GATA4 gene associated with atrioventricular septal defect type 4.	Whole Blood or Buccal Swab	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["GATA4 gene sequence", "Coding region variants", "Exon-intron boundaries"] Parameters [] Preparation ["Attend pre-genetic counseling session", "Provide detailed clinical history and echocardiogram reports"] Indications ["Diagnosis of GATA4-related congenital heart disease", "Family cascade screening", "Reproductive risk assessment"] Measurement technique Confirm with laboratory Codes LOINC: 88827-5 ICD-10: Q21.2 Clinical summary This genetic test identifies mutations in the GATA4 gene associated with atrioventricular septal defect type 4.
TEST-2236 GDF1 Gene Genetic Test for Transposition of the Great Arteries (Dextro‑Looped Type 3) This test identifies mutations in the GDF1 gene associated with dextro-looped transposition of the great arteries (D‑TGA). It uses Next-Generation Sequencing (NGS) to analyze the e...	Peripheral whole blood (2–3 mL EDTA), 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 ["GDF1 gene sequence variants", "Pathogenic mutations in GDF1"] Parameters [] Preparation ["No specific fasting required", "Informed consent and genetic counseling required before sample collection"] Indications ["Diagnosis of dextro-looped transposition of the great arteries (D‑TGA)", "Carrier screening for GDF1 mutations", "Family planning for families with a history of D‑TGA"] Measurement technique Confirm with laboratory Codes LOINC: 55233-1 ICD-10: Q20.3 Clinical summary This test identifies mutations in the GDF1 gene associated with dextro-looped transposition of the great arteries (D‑TGA). It uses Next-Generation Sequencing (NGS) to analyze the entire coding region of the gene.
TEST-3712 GHR Gene Laron Syndrome Genetic Test This test identifies pathogenic variants in the GHR gene to diagnose Laron syndrome (growth hormone insensitivity).	Whole Blood or FTA Card (Peripheral Blood)	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Growth Hormone Receptor (GHR) gene variants", "Single nucleotide variants (SNVs)", "Small insertions/deletions (indels)"] Parameters [] Preparation [] Indications ["Suspected Laron syndrome", "Severe short stature with characteristic biochemical profile"] Measurement technique Confirm with laboratory Codes LOINC: 94233-2 ICD-10: E34.3 Clinical summary This test identifies pathogenic variants in the GHR gene to diagnose Laron syndrome (growth hormone insensitivity).
TEST-2746 GLI2 Gene Holoprosencephaly Type 9 Genetic Test This test detects pathogenic variants in the GLI2 gene associated with holoprosencephaly type 9.	Peripheral whole blood (venipuncture or heel-prick FTA card); or previously extracted DNA	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic single-nucleotide variants in GLI2", "Small insertions/deletions in GLI2"] Parameters [] Preparation ["Mandatory pre-test genetic counseling session", "Provide detailed clinical history, family pedigree, and prior imaging reports"] Indications ["Suspected holoprosencephaly type 9", "Neonatal neurology evaluations", "Dysmorphology evaluations"] Measurement technique Confirm with laboratory Codes LOINC: 82938-1 ICD-10: Q04.2, Q87.0, Z82.79 Clinical summary This test detects pathogenic variants in the GLI2 gene associated with holoprosencephaly type 9.
TEST-5790 GM2A Gene Tay-Sachs Disease AB Variant Genetic Test This diagnostic test evaluates the GM2A gene for pathogenic variants associated with Tay-Sachs disease AB variant (GM2 Activator Deficiency). It identifies mutations causing the co...	Whole Blood (EDTA), Extracted DNA, or FTA Card (Dried Blood Spot)	3 to 4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["GM2A gene sequence", "Copy Number Variants (CNV) within GM2A gene"] Parameters [] Preparation ["No specific fasting required", "No medication or diet adjustments needed prior to testing"] Indications ["Symptomatic patients suspected of GM2A-associated disease", "Family members of individuals diagnosed with GM2A-associated disease", "Couples undergoing carrier screening for Tay-Sachs disease AB variant", "Prenatal diagnosis or PGT following carrier identification"] Measurement technique Confirm with laboratory Codes LOINC: 101346-7 ICD-10: E75.02, Z13.228, Z14.8 Clinical summary This diagnostic test evaluates the GM2A gene for pathogenic variants associated with Tay-Sachs disease AB variant (GM2 Activator Deficiency). It identifies mutations causing the condition.
TEST-3544 GNAS Gene Pseudopseudohypoparathyroidism Genetic Test This diagnostic test evaluates the GNAS gene for mutations associated with pseudopseudohypoparathyroidism.	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 ["GNAS gene mutations", "Exons and splice sites of GNAS"] Parameters [] Preparation ["No specific fasting required", "Do not discontinue prescribed medication"] Indications ["Individuals with phenotypic features of AHO and normal calcium", "Family history of pseudopseudohypoparathyroidism", "Asymptomatic relatives of affected individuals", "Reproductive genetic counselling"] Measurement technique Confirm with laboratory Codes LOINC: 21663-4 ICD-10: E20.8 Clinical summary This diagnostic test evaluates the GNAS gene for mutations associated with pseudopseudohypoparathyroidism.
TEST-5631 GOSR2 Gene Progressive Myoclonus Epilepsy Type 6 Genetic Test This test identifies pathogenic variants in the GOSR2 gene associated with Progressive Myoclonus Epilepsy Type 6 (PME6). It uses Next-Generation Sequencing (NGS) for comprehensive...	Peripheral Whole Blood (3–5 mL in EDTA tube)	3 to 4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["GOSR2 gene coding sequence", "Pathogenic variants in GOSR2"] Parameters [] Preparation ["Pre-test genetic counselling session is mandatory", "Draw a pedigree chart of family members affected"] Indications ["Suspected Progressive Myoclonus Epilepsy Type 6 (PME6)", "Family history suggestive of autosomal recessive inheritance", "Consanguinity", "Cascade screening for at-risk family members"] Measurement technique Confirm with laboratory Codes LOINC: 55233-1 ICD-10: G40.3 Clinical summary This test identifies pathogenic variants in the GOSR2 gene associated with Progressive Myoclonus Epilepsy Type 6 (PME6). It uses Next-Generation Sequencing (NGS) for comprehensive analysis.

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.