Diagnostic options · UAE

Genetics tests in Dubai & UAE

Compare available Genetics 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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2,789

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-1.00–50,000.00 AED

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Genetics test prices

Showing 2551–2565 of 2,789 matching tests.

Genetics diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-5091 TK2 Gene Mitochondrial DNA Depletion Syndrome Genetic Test (NGS) This test detects pathogenic variants in the TK2 gene associated with mitochondrial DNA depletion syndrome.	Whole blood, extracted DNA, dried blood spot (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 ["Pathogenic variants in TK2 gene", "Single nucleotide variants (SNVs)", "Insertions and deletions (indels)", "Copy number variants (CNVs)"] Parameters [] Preparation ["No fasting required.", "Provide detailed clinical history.", "Attend a pre-test genetic counselling session.", "Document a three-generation pedigree."] Indications ["Suspected mitochondrial DNA depletion syndrome", "Family planning for inherited disorders", "Diagnosis of progressive neurological disorders in infancy or childhood"] Measurement technique Confirm with laboratory Codes LOINC: 87809-3 ICD-10: E88.8 Clinical summary This test detects pathogenic variants in the TK2 gene associated with mitochondrial DNA depletion syndrome.
TEST-5696 TMC1 Gene Deafness (Autosomal Dominant Type 36) Genetic Test This test identifies pathogenic variants in the TMC1 gene associated with autosomal dominant non-syndromic hearing loss (DFNA36).	Whole Blood, Extracted DNA, One-drop Blood on 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 TMC1 gene", "Single nucleotide variants (SNVs)", "Small insertions and deletions (indels)"] Parameters [] Preparation ["No specific fasting required", "Inform the lab of any current medications"] Indications ["Diagnosis of autosomal dominant non-syndromic hearing loss (DFNA36)", "Genetic counselling for families with hearing loss", "Assessment of inheritance risk for family members"] Measurement technique Confirm with laboratory Codes LOINC: 82467-3 ICD-10: H90.3, H91.9 Clinical summary This test identifies pathogenic variants in the TMC1 gene associated with autosomal dominant non-syndromic hearing loss (DFNA36).
TEST-5659 TMC1 Gene Deafness Autosomal Recessive Type 7 Genetic Test This genetic test identifies pathogenic variants in the TMC1 gene associated with autosomal recessive non-syndromic hearing loss type 7 (DFNB7). It detects mutations causing severe...	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 TMC1 gene", "Copy number variations (CNVs) in the TMC1 gene"] Parameters [] Preparation ["No fasting required", "No medication changes required"] Indications ["Individuals with congenital or early-onset bilateral hearing loss", "Family history suggesting recessive inheritance of hearing loss", "Preconception carrier screening for couples"] Measurement technique Confirm with laboratory Codes LOINC: 101371-1 ICD-10: H90.3 Clinical summary This genetic test identifies pathogenic variants in the TMC1 gene associated with autosomal recessive non-syndromic hearing loss type 7 (DFNB7). It detects mutations causing severe-to-profound bilateral sensorineural deafness.
TEST-4112 TMCO1 Gene Craniofacial Dysmorphism, Skeletal Anomalies & Mental Retardation Syndrome NGS Test This diagnostic test evaluates the TMCO1 gene for pathogenic variants linked to craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome.	Whole Blood (EDTA), FTA Card Blood Spot, or Extracted DNA	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["TMCO1 gene coding region variants", "Pathogenic mutations"] Parameters [] Preparation ["Attend a pre-test genetic counseling session", "Provide detailed family history"] Indications ["Diagnosis of TMCO1-related syndrome", "Genetic counseling", "Management planning"] Measurement technique Confirm with laboratory Codes LOINC: 102502-1 ICD-10: Q87.8 Clinical summary This diagnostic test evaluates the TMCO1 gene for pathogenic variants linked to craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome.
TEST-5251 TMCO1 Gene Sequencing (NGS) Test This test identifies pathogenic variants in the TMCO1 gene, which are associated with a specific syndrome characterized by craniofacial dysmorphism, skeletal anomalies, and intelle...	Whole Blood (EDTA) or Saliva (Oragene®)	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 TMCO1 gene", "Single-nucleotide variants", "Insertions/deletions", "Copy-number aberrations"] Parameters [] Preparation ["No specific patient preparation required"] Indications ["Suspected TMCO1-related disorder", "Differential diagnosis of craniofacial-skeletal-intellectual disability syndromes"] Measurement technique Confirm with laboratory Codes LOINC: 94222-5 ICD-10: Q87.8, Q87.0, Q75.8 Clinical summary This test identifies pathogenic variants in the TMCO1 gene, which are associated with a specific syndrome characterized by craniofacial dysmorphism, skeletal anomalies, and intellectual disability.
TEST-4577 TMEM138 Gene Joubert Syndrome Type 16 Genetic Test This test evaluates the TMEM138 gene for pathogenic variants associated with Joubert syndrome type 16.	Peripheral whole blood (EDTA) or dried blood spot (DBS)	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["TMEM138 gene sequence", "Deletion/duplication analysis of TMEM138"] Parameters [] Preparation ["No special preparation required"] Indications ["Suspected Joubert syndrome type 16 based on clinical and imaging findings", "Family history of Joubert syndrome type 16"] Measurement technique Confirm with laboratory Codes LOINC: 81409-1 ICD-10: Q04.3 Clinical summary This test evaluates the TMEM138 gene for pathogenic variants associated with Joubert syndrome type 16.
TEST-6268 TMEM165 Gene CDG Type 2K Genetic Test This test identifies pathogenic variants in the TMEM165 gene, confirming a diagnosis of Congenital Disorder of Glycosylation Type 2K (CDG-IIK).	Peripheral Whole Blood (EDTA) 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 (SNVs, indels, CNVs) in the TMEM165 gene", "Defective protein glycosylation pathway"] Parameters [] Preparation ["No fasting required", "Maintain good hydration", "Mandatory pre-test genetic counseling session required"] Indications ["Clinical suspicion of Congenital Disorder of Glycosylation Type 2K (CDG-IIK)", "Patients with symptoms suggestive of a rare metabolic disorder involving glycosylation"] Measurement technique Confirm with laboratory Codes LOINC: 81799-6 ICD-10: E77.8 Clinical summary This test identifies pathogenic variants in the TMEM165 gene, confirming a diagnosis of Congenital Disorder of Glycosylation Type 2K (CDG-IIK).
TEST-4506 TMEM173 Gene (STING) Vasculopathy Genetic Test This test identifies pathogenic variants in the TMEM173 gene, confirming a diagnosis of STING-associated vasculopathy with onset in infancy (SAVI).	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 TMEM173 gene", "Single-nucleotide variants (SNVs)", "Small insertions/deletions (indels)", "Copy number variants (CNVs)"] Parameters [] Preparation ["Mandatory pre-test genetic counseling session.", "No specific fasting required.", "No medication adjustments required unless directed by physician."] Indications ["Suspected STING-associated vasculopathy with onset in infancy (SAVI)", "Unexplained early-onset systemic inflammation", "Skin vasculitis", "Interstitial lung disease"] Measurement technique Confirm with laboratory Codes LOINC: 91856-0 ICD-10: M35.8 Clinical summary This test identifies pathogenic variants in the TMEM173 gene, confirming a diagnosis of STING-associated vasculopathy with onset in infancy (SAVI).
TEST-4584 TMEM231 Gene Joubert Syndrome Type 20 Genetic Test This genetic test identifies pathogenic variants in the TMEM231 gene associated with Joubert syndrome type 20.	Whole blood (3 mL) or saliva	3–4 Weeks (express reporting available)	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in TMEM231 gene", "Copy number variations (deletions/duplications) in TMEM231 gene"] Parameters [] Preparation ["Mandatory genetic counselling session prior to sample collection", "Provide a three-generation family pedigree"] Indications ["Suspected Joubert syndrome type 20", "Neurodevelopmental disorder with characteristic MRI findings"] Measurement technique Confirm with laboratory Codes LOINC: 101356-6 ICD-10: Q04.3 Clinical summary This genetic test identifies pathogenic variants in the TMEM231 gene associated with Joubert syndrome type 20.
TEST-4573 TMEM237 Gene Joubert Syndrome Type 14 Genetic Test This genetic test evaluates the TMEM237 gene for mutations associated with Joubert syndrome type 14.	Whole blood (EDTA), extracted DNA, 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 ["TMEM237 gene sequence", "Copy Number Variants (CNV) in TMEM237"] Parameters [] Preparation ["Genetic counselling is mandatory prior to sample collection"] Indications ["Diagnosis of Joubert syndrome type 14", "Genetic counselling for families with Joubert syndrome"] Measurement technique Confirm with laboratory Codes LOINC: 57555-2 ICD-10: Q04.3 Clinical summary This genetic test evaluates the TMEM237 gene for mutations associated with Joubert syndrome type 14.
TEST-5767 TMEM240 Gene Spinocerebellar Ataxia Type 21, Autosomal Dominant Genetic Test This test identifies pathogenic variants in the TMEM240 gene, the cause of autosomal dominant spinocerebellar ataxia type 21.	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 ["Pathogenic variants in the TMEM240 gene", "Single-nucleotide variants", "Small insertions/deletions", "Copy-number changes"] Parameters [{"name": "Variant Allele Frequency", "reference_range": "Down to 5%"}] Preparation ["No fasting required", "No special preparation needed"] Indications ["Confirmation of clinical diagnosis of SCA21", "Presymptomatic testing for at-risk individuals", "Family planning and genetic counseling"] Measurement technique Confirm with laboratory Codes LOINC: 55233-1 ICD-10: G11.2 Clinical summary This test identifies pathogenic variants in the TMEM240 gene, the cause of autosomal dominant spinocerebellar ataxia type 21.
TEST-4435 TMEM43 Gene Arrhythmogenic Right Ventricular Cardiomyopathy Type 5 Genetic Test This test identifies genetic variants in the TMEM43 gene associated with Arrhythmogenic Right Ventricular Cardiomyopathy Type 5 (ARVC5).	Peripheral whole blood (3–5 mL collected in EDTA tube)	3–4 weeks (21–28 calendar days) from sample receipt	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic and likely pathogenic variants in the TMEM43 gene", "Full coding region coverage of TMEM43"] Parameters [] Preparation [] Indications ["Personal or family history suggestive of ARVC", "Pre-participation cardiac screening for athletes", "Asymptomatic relatives of individuals with identified TMEM43 mutations"] Measurement technique Confirm with laboratory Codes LOINC: 90553-2 ICD-10: I42.80 Clinical summary This test identifies genetic variants in the TMEM43 gene associated with Arrhythmogenic Right Ventricular Cardiomyopathy Type 5 (ARVC5).
TEST-3646 TMEM67 Gene (Meckel Syndrome Type 3) Genetic Test This genetic test identifies pathogenic variants in the TMEM67 gene associated with Meckel syndrome type 3.	Whole Blood (EDTA), Extracted DNA, or FTA Card Spot	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 TMEM67 gene"] Parameters [] Preparation ["No fasting required", "Avoid strenuous exercise 2 hours prior to draw"] Indications ["Suspected Meckel syndrome type 3", "Carrier screening in families with a history of MKS3", "Prenatal diagnosis", "Informed reproductive planning"] Measurement technique Confirm with laboratory Codes LOINC: 81316-6 ICD-10: Q61.9 Clinical summary This genetic test identifies pathogenic variants in the TMEM67 gene associated with Meckel syndrome type 3.
TEST-5077 TMEM70 Gene Analysis (Mitochondrial Complex V Deficiency, Nuclear Type 2) Test This genetic test analyzes the TMEM70 gene to detect pathogenic variants associated with Mitochondrial Complex V (ATP Synthase) Deficiency, Nuclear Type 2.	Whole Blood (EDTA), Extracted DNA, or FTA Card (blood spot)	3 to 4 weeks from sample receipt	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["TMEM70 gene sequence", "Pathogenic variants in TMEM70"] Parameters [] Preparation ["Inform phlebotomist of all current medications, supplements, and herbal preparations.", "No fasting required."] Indications ["Suspected Mitochondrial Complex V Deficiency, Nuclear Type 2", "Infants with unexplained metabolic crises", "Neonates with hypotonia and lactic acidosis"] Measurement technique Confirm with laboratory Codes LOINC: 81337-8 ICD-10: E88.49 Clinical summary This genetic test analyzes the TMEM70 gene to detect pathogenic variants associated with Mitochondrial Complex V (ATP Synthase) Deficiency, Nuclear Type 2.
TEST-5614 TMIE Gene Deafness, Autosomal Recessive Type 6 Genetic Test This diagnostic test evaluates the TMIE gene for pathogenic variants associated with autosomal recessive deafness type 6 (DFNB6). It identifies mutations causing congenital or earl...	Whole Blood (EDTA), Extracted DNA, or FTA card sample	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 TMIE gene", "Single nucleotide variants", "Small indels", "Copy number variants"] Parameters [] Preparation ["No specific fasting required", "Inform phlebotomist of bleeding disorders or severe anaemia"] Indications ["Diagnosis of autosomal recessive deafness type 6 (DFNB6)", "Genetic counselling for families with hearing loss", "Informing family planning and early intervention strategies"] Measurement technique Confirm with laboratory Codes LOINC: 58122-8 ICD-10: H90.3 Clinical summary This diagnostic test evaluates the TMIE gene for pathogenic variants associated with autosomal recessive deafness type 6 (DFNB6). It identifies mutations causing congenital or early-onset sensorineural hearing loss.

Category overview

Genetics: overview

Understanding your unique biological blueprint offers a profound sense of clarity and empowers proactive health planning for you and your family. At DNA Labs UAE, our specialized Genetics division employs state-of-the-art molecular technologies to provide deep insights into hereditary markers and cellular mutations. This comprehensive genetics testing in the UAE equips your healthcare provider with the precise data needed to tailor your medical guidance effectively. Recognized among top diagnostic labs in Dubai and the UAE, we prioritize your peace of mind through strict confidentiality protocols and exceptionally fast, accurate reporting. Take the next step in your health journey. View our genetics diagnostic services, book a private home collection, or consult our specialized team today.

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Genetics tests in Dubai & UAE

Genetics test prices

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