Gene Sequencing tests in Dubai & UAE

Compare available 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

143

Listed price range

2,600.00–3,200.00 AED

Clinical preparation

Confirm test-specific instructions with your clinician or laboratory.

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Gene Sequencing test prices

Showing 61–75 of 143 matching tests.

Gene Sequencing diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-3417 HSD17B3 Gene Genetic Test for Pseudohermaphroditism with Gynecomastia This test identifies pathogenic variants in the HSD17B3 gene, which are associated with 46,XY disorder of sex development (DSD) presenting as pseudohermaphroditism with gynecomasti...	Whole blood (2 mL EDTA), extracted DNA, or FTA card specimen	3 – 4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["HSD17B3 gene sequence", "Pathogenic variants (SNVs, indels, CNVs)"] Parameters [] Preparation ["No fasting required", "Inform lab of anticoagulant medication use"] Indications ["Diagnosis of 46,XY DSD", "Evaluation of impaired testosterone biosynthesis"] Measurement technique Confirm with laboratory Codes LOINC: 21669-6 ICD-10: Q56.4 Clinical summary This test identifies pathogenic variants in the HSD17B3 gene, which are associated with 46,XY disorder of sex development (DSD) presenting as pseudohermaphroditism with gynecomastia.
TEST-5713 IBA57 Gene (Spastic Paraplegia Type 74) Autosomal Recessive Genetic Test This genetic test analyzes the IBA57 gene to detect mutations associated with autosomal recessive spastic paraplegia type 74 (SPG74). It identifies pathogenic variants that disrupt...	Peripheral whole blood (3–5 mL in EDTA tube) or extracted DNA / 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 ["IBA57 gene sequence", "Pathogenic variants in IBA57"] Parameters [] Preparation [] Indications ["Suspected diagnosis of Spastic Paraplegia Type 74 (SPG74)", "Family history of SPG74"] Measurement technique Confirm with laboratory Codes LOINC: 81328-4 ICD-10: G11.4 Clinical summary This genetic test analyzes the IBA57 gene to detect mutations associated with autosomal recessive spastic paraplegia type 74 (SPG74). It identifies pathogenic variants that disrupt the function of the IBA57 protein, leading to the neurological symptoms of the condition.
TEST-5344 IL12RB1 Gene Sequencing for Atypical Mycobacterial Infection (MSMD) Test This test identifies pathogenic variants in the IL12RB1 gene associated with Mendelian Susceptibility to Mycobacterial Disease (MSMD).	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 IL12RB1 gene", "Copy Number Variations (CNVs) in the IL12RB1 gene"] Parameters [] Preparation ["No specific fasting required", "Avoid recent blood transfusion (within 4 weeks)"] Indications ["Suspected Mendelian Susceptibility to Mycobacterial Disease (MSMD)", "Recurrent or severe infections with atypical mycobacteria", "Family history suggestive of MSMD"] Measurement technique Confirm with laboratory Codes LOINC: 83520-5 ICD-10: D84.89 Clinical summary This test identifies pathogenic variants in the IL12RB1 gene associated with Mendelian Susceptibility to Mycobacterial Disease (MSMD).
TEST-6071 ITGB2 Gene Leukocyte Adhesion Deficiency (LAD) Genetic Test This genetic test evaluates the ITGB2 gene for pathogenic variants associated with Leukocyte Adhesion Deficiency type 1 (LAD-1). It provides a definitive molecular diagnosis for th...	Whole Blood (EDTA) or Buccal Swab / FTA Card	3–4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["ITGB2 gene coding region", "Pathogenic variants in ITGB2"] Parameters [] Preparation ["No specific fasting required", "Inform phlebotomist of any bleeding disorders"] Indications ["Clinical suspicion of Leukocyte Adhesion Deficiency type 1 (LAD-1)", "Family history of LAD-1", "Recurrent severe infections without clear cause"] Measurement technique Confirm with laboratory Codes LOINC: 94710-5 ICD-10: D72.0 Clinical summary This genetic test evaluates the ITGB2 gene for pathogenic variants associated with Leukocyte Adhesion Deficiency type 1 (LAD-1). It provides a definitive molecular diagnosis for this rare primary immunodeficiency.
TEST-2920 JAG2 Gene Sequencing Test for Craniofacial and Neurodevelopmental Abnormalities This test identifies pathogenic variants in the JAG2 gene, associated with Alagille syndrome type 2 and related craniofacial dysmorphism syndromes.	Whole blood or dried blood spot (FTA)	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 JAG2 gene", "Sequence-level alterations in coding regions, intron-exon boundaries, and UTRs"] Parameters [] Preparation ["No fasting required", "No specific medication or diet restrictions"] Indications ["Suspected Alagille syndrome type 2", "Pediatric patients with cholestatic jaundice, dysmorphic facies, and neurodevelopmental delay", "Family history of JAG2-related disorders"] Measurement technique Confirm with laboratory Codes LOINC: 51966-0 ICD-10: Q44.7, Q87.8, F84.9 Clinical summary This test identifies pathogenic variants in the JAG2 gene, associated with Alagille syndrome type 2 and related craniofacial dysmorphism syndromes.
TEST-3177 JAK3 Gene Sequencing for SCID (T-Negative, B-Positive) Test This test identifies pathogenic variants in the JAK3 gene, confirming a diagnosis of autosomal recessive SCID with a T-negative, B-positive phenotype.	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 JAK3 gene", "Single-nucleotide variants", "Small insertions and deletions", "Copy-number alterations"] Parameters [] Preparation ["No fasting required", "Pre-test genetic counseling is mandatory"] Indications ["Suspected SCID with T-negative, B-positive phenotype", "Family history of SCID", "Pre-transplant evaluation", "Carrier screening"] Measurement technique Confirm with laboratory Codes LOINC: 94054-7 ICD-10: D81.0, D81.9 Clinical summary This test identifies pathogenic variants in the JAK3 gene, confirming a diagnosis of autosomal recessive SCID with a T-negative, B-positive phenotype.
TEST-5135 KRT10 Gene Epidermolytic Hyperkeratosis Genetic Test This test identifies pathogenic variants in the KRT10 gene associated with epidermolytic hyperkeratosis.	Peripheral whole blood	3–4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Single-nucleotide variants (SNVs)", "Insertions/Deletions (Indels)", "Copy-number changes (CNVs) in the KRT10 gene"] Parameters [] Preparation ["No fasting required", "Continue all prescribed medications unless advised otherwise by a dermatologist"] Indications ["Suspected epidermolytic hyperkeratosis", "Family history of epidermolytic hyperkeratosis", "Guiding treatment decisions"] Measurement technique Confirm with laboratory Codes LOINC: 21663-7 ICD-10: Q80.2 Clinical summary This test identifies pathogenic variants in the KRT10 gene associated with epidermolytic hyperkeratosis.
TEST-5131 KRT5 Gene Epidermolysis Bullosa Simplex Genetic Test This genetic test identifies pathogenic variants in the KRT5 gene associated with Epidermolysis Bullosa Simplex.	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 KRT5 gene", "Full coding region and splice junctions"] Parameters [] Preparation [] Indications ["Suspected Epidermolysis Bullosa Simplex (EBS)", "Family history of EBS", "Need for genetic counselling"] Measurement technique Confirm with laboratory Codes LOINC: 81293-1 ICD-10: Q81.0, Z13.79, Z15.09 Clinical summary This genetic test identifies pathogenic variants in the KRT5 gene associated with Epidermolysis Bullosa Simplex.
TEST-6298 LCAT Gene Fish-Eye Disease Genetic Test This genetic test identifies pathogenic variants in the LCAT gene associated with fish-eye disease and LCAT deficiency.	Peripheral whole blood (EDTA) or FTA card capillary blood	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["LCAT gene sequence", "Pathogenic variants (SNVs, indels, copy-number variants)"] Parameters [] Preparation [] Indications ["Investigate hereditary corneal opacities (fish-eye disease)", "Differentiate LCAT deficiency from other stromal dystrophies", "Screen for metabolic aetiologies in patients with extremely low HDL-cholesterol and arcus cornealis", "Characterize novel LCAT variants", "Study HDL metabolism"] Measurement technique Confirm with laboratory Codes LOINC: 81247-9 ICD-10: H18.2, E78.6 Clinical summary This genetic test identifies pathogenic variants in the LCAT gene associated with fish-eye disease and LCAT deficiency.
TEST-4863 LINS1 Gene Sequencing (NGS) for Intellectual Disability Type 27 Test This test identifies genetic variants in the LINS1 gene associated with intellectual disability type 27.	Peripheral Whole Blood	21–28 Business Days	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["LINS1 gene coding region variants", "LINS1 gene splice-site variants"] Parameters [] Preparation [] Indications ["Suspected intellectual disability type 27", "Family history of intellectual disability type 27", "Genetic counselling for recurrence risk"] Measurement technique Confirm with laboratory Codes LOINC: 81251-6 ICD-10: F78 Clinical summary This test identifies genetic variants in the LINS1 gene associated with intellectual disability type 27.
TEST-4806 LPIN2 Gene Majeed Syndrome Genetic Test This test evaluates the LPIN2 gene for mutations associated with Majeed syndrome.	Whole blood (EDTA) or extracted 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 LPIN2 gene", "Single Nucleotide Variants (SNVs)", "Insertions/Deletions (indels)", "Copy Number Variations (CNVs)"] Parameters [] Preparation ["No specific fasting required", "Inform genetic counselor of current medications"] Indications ["Suspected Majeed syndrome based on clinical presentation", "Family history of Majeed syndrome", "Carrier screening in families with known LPIN2 mutations"] Measurement technique Confirm with laboratory Codes LOINC: 92708-8 ICD-10: M86.3 Clinical summary This test evaluates the LPIN2 gene for mutations associated with Majeed syndrome.
TEST-2220 LRIG2 Gene Urofacial Syndrome Genetic Test This test analyzes the LRIG2 gene for pathogenic variants associated with urofacial syndrome (Ochoa syndrome). It identifies single nucleotide variants, insertions, deletions, and...	Peripheral whole blood (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 ["LRIG2 gene sequence", "Single Nucleotide Variants (SNVs)", "Insertions/Deletions (Indels)", "Copy Number Variations (CNVs)"] Parameters [] Preparation ["No fasting required", "No need to stop medications"] Indications ["Suspected urofacial syndrome (Ochoa syndrome)", "Unexplained dysfunctional voiding", "Recurrent urinary tract infections", "Hydronephrosis", "Facial inversion during laughter"] Measurement technique Confirm with laboratory Codes LOINC: 50121-7 ICD-10: Q87.8 Clinical summary This test analyzes the LRIG2 gene for pathogenic variants associated with urofacial syndrome (Ochoa syndrome). It identifies single nucleotide variants, insertions, deletions, and copy number variations within the gene.
TEST-6097 MAN2B1 Gene Alpha-Mannosidosis Genetic Test This test evaluates the MAN2B1 gene for pathogenic variants associated with Alpha-Mannosidosis.	Peripheral whole blood (EDTA tube) or DNA from 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 MAN2B1 gene", "Single nucleotide variants", "Insertions", "Deletions", "Copy number variations"] Parameters [] Preparation ["No specific fasting required", "Continue all prescribed medications"] Indications ["Diagnosis of Alpha-Mannosidosis", "Carrier screening", "Reproductive risk assessment"] Measurement technique Confirm with laboratory Codes LOINC: 51954-0 ICD-10: E77.1 Clinical summary This test evaluates the MAN2B1 gene for pathogenic variants associated with Alpha-Mannosidosis.
TEST-6101 MBL2 Gene Mannose-Binding Protein Deficiency Genetic Test This genetic test identifies pathogenic variants in the MBL2 gene associated with mannose-binding protein deficiency.	Whole Blood, Extracted DNA, or FTA Card Blood Spot (Peripheral Blood)	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 MBL2 gene", "Mannose-binding lectin 2 gene sequence"] Parameters [] Preparation ["No fasting required"] Indications ["Patients with recurrent sinopulmonary infections", "Comprehensive immunodeficiency workup", "Pedigree analysis", "Pre-test counselling"] Measurement technique Confirm with laboratory Codes LOINC: 81351-9 ICD-10: D84.8 Clinical summary This genetic test identifies pathogenic variants in the MBL2 gene associated with mannose-binding protein deficiency.
TEST-3873 MECP2 Gene (Autism Susceptibility, X-Linked Type 3) Genetic Test This test evaluates the MECP2 gene for mutations associated with Rett syndrome, autism susceptibility, and X-linked intellectual disability.	Peripheral blood (EDTA 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 ["MECP2 gene mutations", "Coding region variants"] Parameters [] Preparation ["A detailed clinical history is required.", "A mandatory genetic counselling session is required before sample collection."] Indications ["Suspected Rett syndrome", "Autism spectrum susceptibility", "X-linked intellectual disability type 3", "Developmental regression"] Measurement technique Confirm with laboratory Codes LOINC: 21637-9 ICD-10: Z13.8 Clinical summary This test evaluates the MECP2 gene for mutations associated with Rett syndrome, autism susceptibility, and X-linked intellectual disability.

Category overview

Gene Sequencing: overview

Achieving a definitive diagnosis for a complex or rare genetic disorder often requires reading the entire genetic code of specific genes to find elusive, hidden errors. As a cornerstone of our advanced Genetics services, Gene Sequencing expansively scans the targeted regions of your genome to uncover rare or novel mutations that standard tests miss. Utilizing state-of-the-art sequencing technology, this comprehensive molecular profiling delivers the critical data necessary to safely guide your healthcare provider in tailoring highly personalized medical management and targeted therapeutic interventions. Trusted for molecular excellence among premier diagnostic labs in the UAE, DNA Labs ensures absolute patient confidentiality, exceptional analytical precision, and remarkably fast reporting. Find the clear, definitive answers you need—schedule your gene sequencing testing in UAE, coordinate a seamless clinical sample transfer, or consult our expert medical genetics professionals today.

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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.