Diagnostic options · UAE

Single Gene tests in Dubai & UAE

Compare available Single Gene 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

332

Listed price range

2,000.00–2,800.00 AED

Clinical preparation

Confirm test-specific instructions with your clinician or laboratory.

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Single Gene test prices

Showing 106–120 of 332 matching tests.

Single Gene diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-2800 FGFR1 Gene Hartsfield Syndrome Genetic Test This test identifies pathogenic mutations within the FGFR1 gene associated with Hartsfield syndrome.	Peripheral whole blood (1 mL)	3 – 4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["FGFR1 gene coding region mutations", "Pathogenic variants"] Parameters [] Preparation [] Indications ["Clinical suspicion of Hartsfield syndrome", "Paediatric patients with characteristic features", "Genetic counselling for families"] Measurement technique Confirm with laboratory Codes LOINC: 82927-8 ICD-10: Q87.8 Clinical summary This test identifies pathogenic mutations within the FGFR1 gene associated with Hartsfield syndrome.
TEST-5355 FGFR2 Gene Bent Bone Dysplasia Syndrome Genetic Test This test evaluates the FGFR2 gene for mutations associated with Bent Bone Dysplasia Syndrome using Next-Generation Sequencing.	Peripheral whole blood	3 – 4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["FGFR2 gene coding region", "FGFR2 gene splice junctions", "Single-nucleotide variants", "Small insertions/deletions", "Copy-number changes"] Parameters [] Preparation ["No specific fasting required", "Do not discontinue prescribed medications without consulting your physician"] Indications ["Suspected Bent Bone Dysplasia Syndrome", "Family history of skeletal dysplasia", "Need for definitive genetic diagnosis"] Measurement technique Confirm with laboratory Codes LOINC: 93296-0 ICD-10: Q78.8 Clinical summary This test evaluates the FGFR2 gene for mutations associated with Bent Bone Dysplasia Syndrome using Next-Generation Sequencing.
TEST-2668 FGFR2 Gene LADD Syndrome Next-Generation Sequencing Genetic Test This diagnostic test evaluates the FGFR2 gene for pathogenic variants associated with Lacrimo-Auriculo-Dento-Digital (LADD) syndrome.	Whole Blood, Extracted DNA, 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 ["FGFR2 gene coding region", "Pathogenic variants (missense, nonsense, splice-site)"] Parameters [] Preparation ["Detailed clinical history required", "Mandatory genetic counseling session"] Indications ["Suspected LADD syndrome", "Pediatric dysmorphology cases", "Familial cases"] Measurement technique Confirm with laboratory Codes LOINC: 21663-3 ICD-10: Q87.0 Clinical summary This diagnostic test evaluates the FGFR2 gene for pathogenic variants associated with Lacrimo-Auriculo-Dento-Digital (LADD) syndrome.
TEST-5151 FKBP14 Gene Ehlers-Danlos Syndrome with Progressive Kyphoscoliosis, Myopathy, and Hearing Loss Genetic Test This genetic test identifies mutations in the FKBP14 gene associated with Ehlers-Danlos syndrome characterized by progressive kyphoscoliosis, myopathy, and hearing loss.	Whole Blood (EDTA) 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 ["FKBP14 gene sequence", "Single nucleotide variants", "Small indels", "Copy Number Variations (CNV)"] Parameters [] Preparation [] Indications ["Clinical suspicion of Ehlers-Danlos syndrome with progressive kyphoscoliosis, myopathy, and hearing loss", "Family history of the disorder"] Measurement technique Confirm with laboratory Codes LOINC: 101554-3 ICD-10: Q79.6, G71.8, H90.3, Z15.89 Clinical summary This genetic test identifies mutations in the FKBP14 gene associated with Ehlers-Danlos syndrome characterized by progressive kyphoscoliosis, myopathy, and hearing loss.
TEST-3059 FLCN Gene (Birt‑Hogg‑Dubé Syndrome) Genetic Test This genetic test identifies mutations in the FLCN gene associated with Birt‑Hogg‑Dubé syndrome.	Whole Blood, 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 ["FLCN gene mutations", "Germline genetic variants"] Parameters [] Preparation ["No fasting or special preparation is required."] Indications ["Suspected Birt‑Hogg‑Dubé syndrome", "Family history of BHD syndrome", "Risk assessment for BHD-related complications"] Measurement technique Confirm with laboratory Codes LOINC: 81304-3 ICD-10: Q89.8 Clinical summary This genetic test identifies mutations in the FLCN gene associated with Birt‑Hogg‑Dubé syndrome.
TEST-5536 FLCN Gene Primary Spontaneous Pneumothorax Genetic Test This genetic test evaluates the FLCN gene for mutations associated with Birt-Hogg-Dubé syndrome, a condition predisposing individuals to primary spontaneous pneumothorax and other...	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 ["FLCN gene sequence", "FLCN gene copy number variations"] Parameters [] Preparation ["No specific fasting required", "No medication adjustments needed"] Indications ["Recurrent primary spontaneous pneumothorax", "Family history of Birt-Hogg-Dubé syndrome", "Suspicion of Birt-Hogg-Dubé syndrome based on clinical features"] Measurement technique Confirm with laboratory Codes LOINC: 87836-3 ICD-10: J93.11 Clinical summary This genetic test evaluates the FLCN gene for mutations associated with Birt-Hogg-Dubé syndrome, a condition predisposing individuals to primary spontaneous pneumothorax and other related health issues.
TEST-4568 FLNB Gene Spondylocarpotarsal Synostosis Syndrome Genetic Test This test analyzes the FLNB gene for mutations associated with spondylocarpotarsal synostosis syndrome.	Whole Blood (EDTA), DNA 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 ["FLNB gene mutations", "Genetic variants"] Parameters [] Preparation [] Indications ["Suspected spondylocarpotarsal synostosis syndrome", "Genetic counseling for skeletal dysplasias"] Measurement technique Confirm with laboratory Codes LOINC: 21658-4 ICD-10: Q87.8 Clinical summary This test analyzes the FLNB gene for mutations associated with spondylocarpotarsal synostosis syndrome.
TEST-4419 FLNC Gene Filaminopathy Genetic Test This test evaluates the FLNC gene for variants associated with filaminopathy, a condition causing muscle weakness and heart problems.	Peripheral Whole Blood	3 – 4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["FLNC gene variants", "Copy Number Variants (CNVs) in FLNC"] Parameters [] Preparation ["Genetic counselling session required before sample collection", "Complete pedigree chart required"] Indications ["Suspected filaminopathy", "Family history of myofibrillar myopathy or restrictive cardiomyopathy", "Unexplained muscle weakness or cardiomyopathy"] Measurement technique Confirm with laboratory Codes LOINC: 78014-3 ICD-10: G71.0, I42.8 Clinical summary This test evaluates the FLNC gene for variants associated with filaminopathy, a condition causing muscle weakness and heart problems.
TEST-2735 FLVCR2 Gene Hydranencephaly, Fowler Type Genetic Test This test analyzes the FLVCR2 gene for pathogenic variants associated with Fowler-type hydranencephaly.	Peripheral 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 ["FLVCR2 gene sequence", "Pathogenic variants in FLVCR2"] Parameters [] Preparation [] Indications ["Suspected Fowler-type hydranencephaly", "Prenatal diagnosis", "Neonatal diagnosis", "Carrier screening", "Reproductive planning"] Measurement technique Confirm with laboratory Codes LOINC: 81724-7 ICD-10: Q04.1, Q04.8, Z13.89 Clinical summary This test analyzes the FLVCR2 gene for pathogenic variants associated with Fowler-type hydranencephaly.
TEST-2632 FOXC2 Gene Lymphedema-Distichiasis Syndrome Genetic Test This test identifies pathogenic variants in the FOXC2 gene associated with lymphedema-distichiasis syndrome.	Whole blood (EDTA) 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 ["FOXC2 gene mutations", "Copy Number Variations (CNVs) in FOXC2"] Parameters [{"name": "Diagnostic Sensitivity", "reference_range": "99.9%"}, {"name": "Methodology", "reference_range": "NGS with CNV analysis"}, {"name": "Coverage", "reference_range": "Full coding exons + 20 bp flanking splice sites"}] Preparation ["No fasting required", "Genetic counselling session mandatory before testing"] Indications ["Diagnosis of lymphedema-distichiasis syndrome", "Family cascade screening for FOXC2 variants", "Prenatal diagnosis (if indicated by family history)"] Measurement technique Confirm with laboratory Codes LOINC: 90362-5 ICD-10: Q87.8, I89.0 Clinical summary This test identifies pathogenic variants in the FOXC2 gene associated with lymphedema-distichiasis syndrome.
TEST-5628 FOXI1 Gene Deafness (Autosomal Recessive Type 4) Genetic Test This test detects pathogenic variants in the FOXI1 gene associated with autosomal recessive nonsyndromic deafness type 4 (DFNB4).	Whole Blood (EDTA), Extracted Genomic 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 FOXI1 gene"] Parameters [] Preparation [] Indications ["Diagnosis of autosomal recessive nonsyndromic deafness type 4 (DFNB4)", "Guidance for cochlear implant candidacy", "Auditory rehabilitation planning", "Family counselling and recurrence risk assessment"] Measurement technique Confirm with laboratory Codes LOINC: 21636-8 ICD-10: H90.3 Clinical summary This test detects pathogenic variants in the FOXI1 gene associated with autosomal recessive nonsyndromic deafness type 4 (DFNB4).
TEST-2832 FREM2 Gene (Fraser Syndrome) Genetic Test This test evaluates the FREM2 gene for pathogenic variants associated with Fraser syndrome.	Whole blood (3–5 mL in EDTA tube), extracted DNA, or dried blood spot	3–4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["FREM2 gene sequence", "Pathogenic variants (SNVs, indels, CNVs)"] Parameters [] Preparation ["No fasting required", "No special preparation needed"] Indications ["Suspected Fraser syndrome", "Family history of Fraser syndrome", "Genetic counselling for family planning"] Measurement technique Confirm with laboratory Codes LOINC: 83325-4 ICD-10: Q87.0 Clinical summary This test evaluates the FREM2 gene for pathogenic variants associated with Fraser syndrome.
TEST-3169 GATA1 Gene Sequencing for X-Linked Thrombocytopenia with Beta-Thalassemia Test This diagnostic test evaluates the GATA1 gene for mutations associated with X-linked thrombocytopenia with beta-thalassemia.	Peripheral whole blood (standard venipuncture or FTA card)	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["GATA1 gene sequence", "Mutations causing X-linked thrombocytopenia with beta-thalassemia"] Parameters [] Preparation ["No specific fasting required", "Do not discontinue prescribed medication without consulting your doctor"] Indications ["Suspected X-linked thrombocytopenia with beta-thalassemia", "Family history of the disorder", "Evaluation of unexplained thrombocytopenia and anaemia"] Measurement technique Confirm with laboratory Codes LOINC: 82994-6 ICD-10: D56.1, D69.42, Z15.89 Clinical summary This diagnostic test evaluates the GATA1 gene for mutations associated with X-linked thrombocytopenia with beta-thalassemia.
TEST-3130 GATA1 Gene Thrombocytopenia, X-Linked Genetic Test This test identifies pathogenic variants in the GATA1 gene associated with X-linked thrombocytopenia.	Peripheral Whole Blood, Buccal Swab, 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 ["GATA1 gene variants", "Pathogenic mutations"] Parameters [] Preparation ["No specific fasting required", "Inform phlebotomist of any medications"] Indications ["Suspected X-linked thrombocytopenia", "Family history of inherited bleeding disorders", "Need for genetic counseling"] Measurement technique Confirm with laboratory Codes LOINC: 94497-8 ICD-10: D69.2 Clinical summary This test identifies pathogenic variants in the GATA1 gene associated with X-linked thrombocytopenia.
TEST-3367 GATA4 Gene Testicular Anomalies with or without Congenital Heart Disease Genetic Test This test evaluates the GATA4 gene for pathogenic variants linked to congenital heart defects and testicular anomalies.	Whole Blood / Peripheral Blood	21–28 working days	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["GATA4 gene sequence", "Pathogenic variants in GATA4"] Parameters [] Preparation ["No fasting required"] Indications ["Suspected GATA4-related congenital heart disease", "Suspected GATA4-related testicular anomalies", "Family history of GATA4-related conditions"] Measurement technique Confirm with laboratory Codes LOINC: 93935-6 ICD-10: Q53.9, Q21.9 Clinical summary This test evaluates the GATA4 gene for pathogenic variants linked to congenital heart defects and testicular anomalies.

Category overview

Single Gene: overview

When clinical symptoms or family history point directly toward a specific inherited condition, highly focused genetic testing provides the exact, rapid insights necessary for peace of mind. Integrated into our advanced Molecular Genetics services, Single Gene testing meticulously analyzes one specific gene for known disease-causing mutations. Utilizing cutting-edge diagnostic technology, this highly focused molecular screening helps confirm or rule out precise genetic traits, safely guiding targeted medical interventions and family planning strategies. Recognized for specialized diagnostic excellence among diagnostic labs in the UAE, DNA Labs ensures absolute patient confidentiality, exceptional analytical precision, and incredibly efficient turnaround times. Take an informed step forward in your health journey—schedule your single gene testing in UAE, book a secure home sample collection, or reach out to our expert medical 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.