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

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Single Gene test prices

Showing 16–30 of 332 matching tests.

Single Gene diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-5271 ALDH18A1 Gene (Cutis Laxa Type 3A, Autosomal Recessive) Genetic Test This genetic test evaluates the ALDH18A1 gene for mutations associated with autosomal recessive cutis laxa type 3A (ARCL3A). It identifies disease-causing variants to confirm the d...	Whole Blood (Peripheral Venous)	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["ALDH18A1 gene sequence", "Disease-causing mutations"] Parameters [{"name": "Coverage", "reference_range": "Full ALDH18A1 gene (all exons and flanking regions)"}, {"name": "Sensitivity", "reference_range": ">99.9% (NGS with >1000x depth)"}] Preparation ["No specific fasting required", "Do not discontinue prescribed medication"] Indications ["Suspected diagnosis of autosomal recessive cutis laxa type 3A", "Family history of ARCL3A"] Measurement technique Confirm with laboratory Codes LOINC: 21639-0 ICD-10: Q82.8 Clinical summary This genetic test evaluates the ALDH18A1 gene for mutations associated with autosomal recessive cutis laxa type 3A (ARCL3A). It identifies disease-causing variants to confirm the diagnosis.
TEST-6361 ALG1 Gene Glycosylation Disorder Type 1K Genetic Test This test detects pathogenic variants in the ALG1 gene associated with Congenital Disorder of Glycosylation Type Ik (CDG-Ik).	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 ["Pathogenic variants in the ALG1 gene", "Single nucleotide variants", "Small insertions and deletions", "Splice-site mutations"] Parameters [] Preparation ["No fasting required.", "Complete a pre-test genetic counselling session.", "Provide a detailed three-generation family pedigree chart."] Indications ["Clinical suspicion of CDG-Ik", "Evaluation of rare inborn errors of metabolism"] Measurement technique Confirm with laboratory Codes LOINC: 50398-0 ICD-10: E77.8 Clinical summary This test detects pathogenic variants in the ALG1 gene associated with Congenital Disorder of Glycosylation Type Ik (CDG-Ik).
TEST-5965 ALPL Gene Odontohypophosphatasia Genetic Test This test analyzes the entire ALPL gene to identify mutations causing Odontohypophosphatasia.	Whole blood, 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 ["ALPL gene sequence", "Single nucleotide variants", "Small insertions and deletions", "Copy number alterations"] Parameters [] Preparation [] Indications ["Suspected Odontohypophosphatasia", "Differential diagnosis of metabolic bone disorders", "Carrier screening for at-risk family members"] Measurement technique Confirm with laboratory Codes LOINC: 94831-8 ICD-10: E83.39 Clinical summary This test analyzes the entire ALPL gene to identify mutations causing Odontohypophosphatasia.
TEST-4683 AMER1 Gene Osteopathia Striata with Cranial Sclerosis Genetic Test This genetic test evaluates the AMER1 gene for pathogenic variants associated with Osteopathia Striata with Cranial Sclerosis.	Whole Blood (EDTA), 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 ["Pathogenic variants in the AMER1 gene"] Parameters [] Preparation ["Complete a comprehensive clinical history form", "Attend a pre-test genetic counselling session"] Indications ["Individuals with clinical signs of osteopathia striata with cranial sclerosis", "At-risk family members", "Prenatal diagnosis in families with an identified AMER1 variant", "Asymptomatic carriers", "Differential diagnosis for sclerosing bone disorders"] Measurement technique Confirm with laboratory Codes LOINC: 94531-1 ICD-10: Q78.8 Clinical summary This genetic test evaluates the AMER1 gene for pathogenic variants associated with Osteopathia Striata with Cranial Sclerosis.
TEST-4973 ANK3 Gene Mental Retardation, Autosomal Recessive Type 37 (MRT37) Genetic Test This genetic test identifies pathogenic variants within the ANK3 gene associated with autosomal recessive intellectual disability type 37 (MRT37).	Whole Blood (3-5 mL EDTA), Extracted DNA, or FTA Card	3–4 weeks from sample receipt	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["ANK3 gene sequence", "Pathogenic variants in ANK3"] Parameters [] Preparation ["Pre-test genetic counseling session required", "Obtain informed consent"] Indications ["Confirmation of clinical diagnosis for MRT37", "Genetic counseling for intellectual disability", "Family planning in cases of suspected recessive inheritance"] Measurement technique Confirm with laboratory Codes LOINC: 93928-2 ICD-10: F78.8 Clinical summary This genetic test identifies pathogenic variants within the ANK3 gene associated with autosomal recessive intellectual disability type 37 (MRT37).
TEST-2686 ANKRD11 Gene Genetic Test for KBG Syndrome This test evaluates the ANKRD11 gene for pathogenic variants associated with KBG syndrome.	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 ["Pathogenic variants in the ANKRD11 gene", "Single nucleotide variants (SNVs)", "Insertions/deletions (indels)", "Small copy number variations (CNVs)"] Parameters [] Preparation [] Indications ["Clinical suspicion of KBG syndrome", "Confirmation of diagnosis"] Measurement technique Confirm with laboratory Codes LOINC: 81263-6 ICD-10: Q87.89 Clinical summary This test evaluates the ANKRD11 gene for pathogenic variants associated with KBG syndrome.
TEST-5777 AP4S1 Gene (SPG52) Genetic Test This test analyzes the AP4S1 gene to detect pathogenic variants associated with Hereditary Spastic Paraplegia Type 52 (SPG52).	Whole Blood (EDTA), Extracted DNA, or FTA Card Dried Blood 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 AP4S1 gene coding region and splice-site junctions", "Presence or absence of mutations causing SPG52"] Parameters [] Preparation ["Clinical history review", "Genetic counseling session", "Routine blood draw (no fasting needed)"] Indications ["Clinical suspicion of Hereditary Spastic Paraplegia Type 52 (SPG52)", "Family history of SPG52", "Neurological symptoms consistent with SPG52"] Measurement technique Confirm with laboratory Codes LOINC: 93437-5 ICD-10: G11.4, Z13.71 Clinical summary This test analyzes the AP4S1 gene to detect pathogenic variants associated with Hereditary Spastic Paraplegia Type 52 (SPG52).
TEST-5770 AP5Z1 Gene SPG48 Genetic Test This test sequences the AP5Z1 gene using NGS to detect mutations causing hereditary spastic paraplegia type 48 (SPG48). It identifies single-nucleotide variants, small insertions/d...	Peripheral Whole Blood (3–5 mL EDTA) or FTA Card Finger-Prick	3 to 4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["AP5Z1 gene sequence", "Single-nucleotide variants", "Small insertions/deletions", "Copy-number variants"] Parameters [] Preparation ["No fasting required", "No special preparation required"] Indications ["Clinical suspicion of SPG48", "Family history of hereditary spastic paraplegia", "Carrier screening for SPG48"] Measurement technique Confirm with laboratory Codes LOINC: 82675-3 ICD-10: G11.4, Z13.7 Clinical summary This test sequences the AP5Z1 gene using NGS to detect mutations causing hereditary spastic paraplegia type 48 (SPG48). It identifies single-nucleotide variants, small insertions/deletions, and copy-number variants.
TEST-5415 APC2-Related Neurodevelopmental Disorder Genetic Test This test detects pathogenic variants in the APC2 gene associated with neurodevelopmental delays and intellectual disability.	Peripheral whole blood (EDTA) 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 APC2 gene", "Single nucleotide variants (SNVs)", "Small insertions/deletions (indels)", "Splice-site alterations"] Parameters [] Preparation [] Indications ["Individuals with clinical features suggestive of APC2-related neurodevelopmental disorder", "Family history of APC2-related disorders", "Diagnostic confirmation"] Measurement technique Confirm with laboratory Codes LOINC: 74092-0 ICD-10: F84.9 Clinical summary This test detects pathogenic variants in the APC2 gene associated with neurodevelopmental delays and intellectual disability.
TEST-5487 ARHGAP31 Gene Adams-Oliver Syndrome Type 1 Genetic Test This test evaluates the ARHGAP31 gene for mutations associated with Adams-Oliver syndrome type 1.	Peripheral Whole Blood or Extracted DNA	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["ARHGAP31 gene sequence", "Point mutations", "Small insertions/deletions", "Copy number variants"] Parameters [] Preparation [] Indications ["Suspected Adams-Oliver syndrome type 1", "Confirmation of clinical diagnosis"] Measurement technique Confirm with laboratory Codes LOINC: 82371-6 ICD-10: Q87.2 Clinical summary This test evaluates the ARHGAP31 gene for mutations associated with Adams-Oliver syndrome type 1.
TEST-3994 ASCL1 Gene Central Hypoventilation Syndrome (Congenital) Genetic Test This test identifies pathogenic variants in the ASCL1 gene associated with Congenital Central Hypoventilation Syndrome (CCHS). It uses Next-Generation Sequencing (NGS) for comprehe...	Whole Blood (EDTA), Extracted DNA, or FTA Card Blood Spot	21–28 Days	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the ASCL1 gene", "Single nucleotide variants (SNVs)", "Small insertions or deletions (indels)", "Large copy number variants (deletions/duplications)"] Parameters [] Preparation ["No fasting required", "No medication adjustments required"] Indications ["Clinical suspicion of Congenital Central Hypoventilation Syndrome (CCHS)", "Individuals with unexplained alveolar hypoventilation or autonomic dysregulation"] Measurement technique Confirm with laboratory Codes LOINC: 94219-7 ICD-10: G47.69 Clinical summary This test identifies pathogenic variants in the ASCL1 gene associated with Congenital Central Hypoventilation Syndrome (CCHS). It uses Next-Generation Sequencing (NGS) for comprehensive analysis.
TEST-6072 ATIC Gene AICA-Ribosiduria due to ATIC Deficiency Genetic Test This genetic test identifies pathogenic variants in the ATIC gene associated with AICA-ribosiduria, an autosomal recessive disorder of purine metabolism.	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 ["Pathogenic variants in the ATIC gene"] Parameters [] Preparation ["Mandatory genetic counselling session", "Provide complete clinical history", "No fasting required"] Indications ["Diagnosis of AICA-ribosiduria", "Carrier screening for AICA-ribosiduria", "Prenatal diagnosis"] Measurement technique Confirm with laboratory Codes LOINC: 81247-9 ICD-10: E79.8 Clinical summary This genetic test identifies pathogenic variants in the ATIC gene associated with AICA-ribosiduria, an autosomal recessive disorder of purine metabolism.
TEST-5438 ATP2A2 Gene Genetic Test for Acrokeratosis Verruciformis (Darier Disease) This genetic test identifies mutations in the ATP2A2 gene associated with Darier disease (acrokeratosis verruciformis).	Whole blood (EDTA), dried blood spot on 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 ["ATP2A2 gene sequence", "Pathogenic variants", "Copy number variations (CNV) within the ATP2A2 gene"] Parameters [] Preparation [] Indications ["Suspected Darier disease", "Family history of Darier disease", "Prenatal or preimplantation genetic diagnosis after identifying a familial variant"] Measurement technique Confirm with laboratory Codes LOINC: 94222-8 ICD-10: Q82.8 Clinical summary This genetic test identifies mutations in the ATP2A2 gene associated with Darier disease (acrokeratosis verruciformis).
TEST-4465 ATP6V0A2 Gene Wrinkly Skin Syndrome Genetic Test This genetic test analyzes the ATP6V0A2 gene to identify pathogenic variants associated with wrinkly skin syndrome.	Blood, DNA FTA Card, Extracted DNA	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["ATP6V0A2 gene sequence", "Single-nucleotide variants", "Small insertions/deletions", "Copy-number variants (CNVs)"] Parameters [] Preparation ["No fasting required.", "Providing a clinical history and a genetic counseling pedigree chart is recommended."] Indications ["Diagnosis of wrinkly skin syndrome", "Carrier screening for family planning"] Measurement technique Confirm with laboratory Codes LOINC: 21665-9 ICD-10: Q82.8 Clinical summary This genetic test analyzes the ATP6V0A2 gene to identify pathogenic variants associated with wrinkly skin syndrome.
TEST-3536 ATP6V1B1 Gene Renal Tubular Acidosis with Deafness Genetic Test This test identifies pathogenic variants in the ATP6V1B1 gene associated with distal renal tubular acidosis and sensorineural deafness.	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 ["ATP6V1B1 gene variants", "Pathogenic mutations"] Parameters [] Preparation ["No fasting required", "Provide detailed medical history and list of current medications"] Indications ["Confirmation of clinical suspicion of dRTA with deafness", "Carrier testing", "Prenatal diagnosis"] Measurement technique Confirm with laboratory Codes LOINC: 21636-6 ICD-10: N25.89 Clinical summary This test identifies pathogenic variants in the ATP6V1B1 gene associated with distal renal tubular acidosis and sensorineural deafness.

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.