Single Gene Analysis tests in Dubai & UAE

Compare available Single Gene Analysis tests, their listed prices and the information provided for each option. Test selection and preparation should be discussed with your clinician.

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Listed price range

2,800.00 AED

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Single Gene Analysis test prices

Showing 16–26 of 26 matching tests.

Single Gene Analysis diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-6148 MRPS16 Gene Test This test identifies pathogenic variants in the MRPS16 gene associated with Combined Oxidative Phosphorylation Deficiency Type 2 (COXPD2). It utilizes Next-Generation Sequencing fo...	Peripheral Blood (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 MRPS16 gene", "Mitochondrial dysfunction related to MRPS16"] Parameters [] Preparation ["No specific fasting required.", "Do not discontinue prescribed medication."] Indications ["Diagnosis of Combined Oxidative Phosphorylation Deficiency Type 2 (COXPD2)", "Patients with suspected mitochondrial disease"] Measurement technique Confirm with laboratory Codes LOINC: 82545-9 ICD-10: E74.89 Clinical summary This test identifies pathogenic variants in the MRPS16 gene associated with Combined Oxidative Phosphorylation Deficiency Type 2 (COXPD2). It utilizes Next-Generation Sequencing for comprehensive analysis.
TEST-4996 NIPAL4 Gene (Congenital Ichthyosiform Erythroderma, Nonbullous Type 1) Genetic Test This genetic test identifies mutations in the NIPAL4 gene associated with nonbullous congenital ichthyosiform erythroderma.	Peripheral Whole Blood, Extracted DNA, or FTA Card 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 NIPAL4 gene", "Exonic and splice-site variants"] Parameters [] Preparation ["No special preparation required", "Continue prescribed medications unless advised otherwise by physician", "Inform phlebotomist about anticoagulant therapy or bleeding tendencies"] Indications ["Clinical suspicion of nonbullous congenital ichthyosiform erythroderma", "Family history of congenital ichthyosis", "Carrier screening in families with affected individuals"] Measurement technique Confirm with laboratory Codes LOINC: 48018-6 ICD-10: Q80.2 Clinical summary This genetic test identifies mutations in the NIPAL4 gene associated with nonbullous congenital ichthyosiform erythroderma.
TEST-3854 PREPL Gene Cystinuria Genetic Test This test identifies pathogenic mutations in the PREPL gene associated with hypotonia-cystinuria syndrome.	Peripheral Whole Blood (EDTA)	21–28 Working Days	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic mutations in the PREPL gene", "Copy number variations (deletions/duplications) in the PREPL gene"] Parameters [] Preparation ["Provide a detailed three-generation pedigree chart.", "Attend a mandatory pre-test genetic counselling session.", "No dietary or drug restrictions are necessary."] Indications ["Diagnosis of hypotonia-cystinuria syndrome", "Carrier screening for at-risk family members", "Evaluation of unexplained cystinuria or hypotonia"] Measurement technique Confirm with laboratory Codes LOINC: 81260-9 ICD-10: E72.0 Clinical summary This test identifies pathogenic mutations in the PREPL gene associated with hypotonia-cystinuria syndrome.
TEST-3502 SIX5 Gene Branchio-Oto-Renal (BOR) Syndrome Type 2 Genetic Test This test identifies pathogenic variants in the SIX5 gene to diagnose Branchio-Oto-Renal (BOR) syndrome type 2.	Peripheral whole 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 SIX5 gene"] Parameters [] Preparation ["No fasting required", "Maintain normal hydration", "Provide complete clinical history and three-generation family pedigree", "Inform phlebotomist of bleeding disorders or anticoagulant use"] Indications ["Suspected Branchio-Oto-Renal syndrome type 2", "Family history of BOR syndrome", "Genetic counseling for related conditions"] Measurement technique Confirm with laboratory Codes LOINC: 81247-9 ICD-10: Q87.8 Clinical summary This test identifies pathogenic variants in the SIX5 gene to diagnose Branchio-Oto-Renal (BOR) syndrome type 2.
TEST-2263 TANC2 Gene NGS Test for Brain Disorders The TANC2 Gene NGS Test detects pathogenic variants in the TANC2 gene associated with neurodevelopmental disorders.	Peripheral 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 ["Pathogenic variants in the TANC2 gene", "Copy Number Variations (CNVs) in TANC2"] Parameters [] Preparation ["No specific fasting required", "Inform lab of recent blood transfusions (within 2 weeks)"] Indications ["Suspected TANC2-related neurodevelopmental disorder", "Family history of TANC2-related disorders", "Genetic counseling for neurodevelopmental conditions"] Measurement technique Confirm with laboratory Codes LOINC: 95900-9 ICD-10: Q87.8, G93.89, Z15.89 Clinical summary The TANC2 Gene NGS Test detects pathogenic variants in the TANC2 gene associated with neurodevelopmental disorders.
TEST-3907 TMLHE Gene Sequencing for X-Linked Autism Susceptibility Type 6 (NGS) Test This diagnostic test evaluates the TMLHE gene for pathogenic variants associated with X-linked autism susceptibility type 6.	Peripheral Whole Blood (EDTA) or Saliva Sample	14–21 Working Days (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 TMLHE gene"] Parameters [] Preparation ["Genetic counseling session required", "No fasting or medication changes needed unless advised by physician"] Indications ["Suspected X-linked autism susceptibility", "Family planning", "Genetic risk assessment"] Measurement technique Confirm with laboratory Codes LOINC: 51995-8 ICD-10: Z15.89 Clinical summary This diagnostic test evaluates the TMLHE gene for pathogenic variants associated with X-linked autism susceptibility type 6.
TEST-2862 TP63 Gene Ectrodactyly-Ectodermal Dysplasia-Cleft Lip/Palate Syndrome Type 3 (EEC3) Genetic Test This genetic test analyzes the TP63 gene to detect mutations associated with Ectrodactyly-Ectodermal Dysplasia-Cleft Lip/Palate Syndrome Type 3 (EEC3). It identifies single nucleot...	Peripheral Whole Blood (EDTA tube), Buccal Swab, or FTA Card	3–4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["TP63 gene variants", "Single nucleotide variants", "Small insertions/deletions", "Copy number alterations"] Parameters [] Preparation ["No specific fasting required", "Inform lab of recent blood transfusions"] Indications ["Suspected diagnosis of EEC syndrome type 3", "Genetic counseling for families with EEC syndrome type 3", "Prenatal diagnosis in high-risk pregnancies"] Measurement technique Confirm with laboratory Codes LOINC: 21636-6 ICD-10: Q87.2 Clinical summary This genetic test analyzes the TP63 gene to detect mutations associated with Ectrodactyly-Ectodermal Dysplasia-Cleft Lip/Palate Syndrome Type 3 (EEC3). It identifies single nucleotide variants, small insertions/deletions, and copy number alterations within the gene.
TEST-2704 TTC7A Gene Sequencing Test This test evaluates the TTC7A gene for pathogenic variants linked to multiple intestinal atresia and combined immunodeficiency.	Whole blood, DNA, or dry 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 TTC7A gene", "Copy Number Variations (CNV) within the TTC7A gene"] Parameters [] Preparation ["No special preparation required", "Prior genetic counseling recommended"] Indications ["Diagnosis of multiple intestinal atresia", "Evaluation of combined immunodeficiency", "Genetic counseling for families with affected individuals", "Prenatal diagnosis (with prior counseling and variant confirmation)"] Measurement technique Confirm with laboratory Codes LOINC: 81255-6 ICD-10: Q41.8 Clinical summary This test evaluates the TTC7A gene for pathogenic variants linked to multiple intestinal atresia and combined immunodeficiency.
TEST-4147 TUBB3 Gene Cortical Dysplasia, Complex, With Other Brain Malformations Type 1 Genetic Test This test identifies pathogenic variants in the TUBB3 gene associated with complex cortical dysplasia with other brain malformations type 1 (CDCBM1).	Peripheral Whole Blood	3–4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in TUBB3 gene exons", "Pathogenic variants in TUBB3 gene splice junctions"] Parameters [] Preparation ["No specific fasting required", "Avoid allogeneic blood transfusion within the past 2 weeks"] Indications ["Suspected complex cortical dysplasia with other brain malformations type 1 (CDCBM1)", "Diagnostic odyssey in families with complex developmental brain malformations"] Measurement technique Confirm with laboratory Codes LOINC: 81313-5 ICD-10: Q04.8 Clinical summary This test identifies pathogenic variants in the TUBB3 gene associated with complex cortical dysplasia with other brain malformations type 1 (CDCBM1).
TEST-2743 ZIC2 Gene Holoprosencephaly Type 5 Genetic Test This diagnostic test evaluates the ZIC2 gene for pathogenic variants associated with holoprosencephaly type 5.	Whole Blood (EDTA), 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 ZIC2 gene"] Parameters [] Preparation [] Indications ["Suspected holoprosencephaly type 5", "Genetic confirmation of ZIC2-related disorder"] Measurement technique Confirm with laboratory Codes LOINC: 21636-6 ICD-10: Q04.2 Clinical summary This diagnostic test evaluates the ZIC2 gene for pathogenic variants associated with holoprosencephaly type 5.
TEST-3949 ZNF778 Gene-Associated Autism: Genetic Test This test identifies pathogenic variants in the ZNF778 gene associated with autism spectrum disorder.	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 ZNF778 gene"] Parameters [] Preparation [] Indications ["Suspected ZNF778-related autism", "Genetic counseling for families with autism spectrum disorder"] Measurement technique Confirm with laboratory Codes LOINC: 21636-6 ICD-10: F84.0 Clinical summary This test identifies pathogenic variants in the ZNF778 gene associated with autism spectrum disorder.

Category overview

Single Gene Analysis: overview

Securing precise diagnostic confirmation for a suspected hereditary condition demands a deeply focused, high-resolution analytical approach to ensure absolute clarity. As a specialized offering within our Genetics department, Single Gene Analysis dives deeply into a targeted section of your DNA to identify intricate molecular changes associated with a known familial disease. By leveraging state-of-the-art diagnostic technology, this precise genomic screening delivers the definitive data needed to assess your risks, safely guiding personalized preventative care and specialized medical oversight. Highly regarded among premier diagnostic labs in Dubai and the UAE, DNA Labs guarantees strict patient confidentiality, uncompromising diagnostic accuracy, and prompt reporting for sensitive cases. Protect your long-term health—book your single gene analysis in UAE, coordinate a comfortable home sample collection, or connect with our specialized genetic counselors.

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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.