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 46–60 of 332 matching tests.

Single Gene diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-3424 CATSPER2 Gene (Deafness & Male Infertility) NGS Test This diagnostic test evaluates the entire coding region and splice sites of the CATSPER2 gene for pathogenic variants linked to deafness and male infertility.	Whole Blood (EDTA) or Dried Blood Spot (FTA Card)	21–28 Business Days	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["CATSPER2 gene sequence", "Copy Number Variants (CNV) in CATSPER2 gene"] Parameters [] Preparation [] Indications ["Deafness work-up", "Infertility work-up", "Carrier screening", "Reproductive planning", "Familial variant confirmation"] Measurement technique Confirm with laboratory Codes LOINC: 94490-1 ICD-10: H90.5 / N46.0 Clinical summary This diagnostic test evaluates the entire coding region and splice sites of the CATSPER2 gene for pathogenic variants linked to deafness and male infertility.
TEST-2059 CBL Gene Juvenile Myelomonocytic Leukemia (JMML) Genetic Test This test identifies germline mutations in the CBL gene associated with an increased risk of developing Juvenile Myelomonocytic Leukemia (JMML).	Whole blood, extracted DNA, 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 ["Germline CBL gene mutations", "Pathogenic variants (SNVs, indels, CNVs)"] Parameters [] Preparation ["No specific fasting required", "Inform lab of any medications"] Indications ["Diagnosis of JMML", "Risk assessment for JMML", "Diagnosis of Noonan-like RASopathy"] Measurement technique Confirm with laboratory Codes LOINC: 60348-4 ICD-10: C93.1 Clinical summary This test identifies germline mutations in the CBL gene associated with an increased risk of developing Juvenile Myelomonocytic Leukemia (JMML).
TEST-5224 CDH3 Gene Ectodermal Dysplasia, Ectrodactyly, and Macular Dystrophy Genetic Test This genetic test analyzes the CDH3 gene to detect mutations associated with Ectodermal Dysplasia, Ectrodactyly, and Macular Dystrophy (EEM) 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 ["CDH3 gene coding regions", "CDH3 gene splice sites", "Copy number variants (CNVs) in CDH3"] Parameters [] Preparation ["No fasting required", "Avoid strenuous exercise 24 hours before collection"] Indications ["Suspected EEM syndrome based on clinical presentation", "Family history of EEM syndrome", "Need for definitive molecular diagnosis for genetic counseling"] Measurement technique Confirm with laboratory Codes LOINC: 21665-2 ICD-10: Q82.4, Q71.6, H35.38 Clinical summary This genetic test analyzes the CDH3 gene to detect mutations associated with Ectodermal Dysplasia, Ectrodactyly, and Macular Dystrophy (EEM) syndrome.
TEST-2562 CDK5RAP2 Gene Microcephaly, Autosomal Recessive Type 3 Genetic Test This test detects pathogenic variants in the CDK5RAP2 gene associated with autosomal recessive primary microcephaly type 3 (MCPH3).	Peripheral Blood or Buccal Swab	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 CDK5RAP2 gene"] Parameters [] Preparation ["Pre-test genetic counseling session is mandatory"] Indications ["Suspected autosomal recessive primary microcephaly type 3 (MCPH3)", "Family history of MCPH3"] Measurement technique Confirm with laboratory Codes LOINC: 94222-8 ICD-10: Q02 Clinical summary This test detects pathogenic variants in the CDK5RAP2 gene associated with autosomal recessive primary microcephaly type 3 (MCPH3).
TEST-2567 CDK6 Gene Microcephaly, Autosomal Recessive Type 12 Genetic Test This test identifies pathogenic mutations in the CDK6 gene associated with autosomal recessive primary microcephaly type 12.	Peripheral Whole Blood (EDTA), 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 ["Pathogenic mutations in the CDK6 gene", "Full gene coverage"] Parameters [] Preparation ["No fasting required unless combined with other bloodwork", "Bring prior medical records, neuroimaging reports, and family history documentation"] Indications ["Clinical suspicion of autosomal recessive primary microcephaly type 12", "Family history of CDK6-related disorders", "Carrier screening", "Prenatal diagnosis"] Measurement technique Confirm with laboratory Codes LOINC: 21636-5 ICD-10: Q02 Clinical summary This test identifies pathogenic mutations in the CDK6 gene associated with autosomal recessive primary microcephaly type 12.
TEST-2750 CDON Gene Holoprosencephaly Type 11 (HPE11) Genetic Test This genetic test evaluates the CDON gene for pathogenic variants associated with Holoprosencephaly type 11 (HPE11).	Whole Blood (EDTA), Dried Blood Spot (FTA Card), or Extracted DNA	3 to 4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["CDON gene pathogenic variants"] Parameters [] Preparation ["No specific fasting required", "Inform phlebotomist of anticoagulants or bleeding diathesis"] Indications ["Suspected Holoprosencephaly type 11", "Family history of HPE11", "Prenatal screening findings suggestive of HPE11"] Measurement technique Confirm with laboratory Codes LOINC: 94800-0 ICD-10: Q04.2 Clinical summary This genetic test evaluates the CDON gene for pathogenic variants associated with Holoprosencephaly type 11 (HPE11).
TEST-5010 CDSN Gene Hypotrichosis Type 2 Genetic Test This test detects pathogenic variants in the CDSN gene associated with autosomal recessive hypotrichosis type 2.	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 CDSN gene"] Parameters [] Preparation ["No special preparation required", "Provide detailed clinical history", "Pre-test genetic counseling recommended"] Indications ["Diagnosis of autosomal recessive hypotrichosis type 2", "Carrier screening", "Family planning guidance", "Differential diagnosis"] Measurement technique Confirm with laboratory Codes LOINC: 92039-4 ICD-10: Q84.0 Clinical summary This test detects pathogenic variants in the CDSN gene associated with autosomal recessive hypotrichosis type 2.
TEST-2781 CFC1 Gene Heterotaxy, Visceral Type 2 Genetic Test This test evaluates the CFC1 gene for pathogenic variants associated with Heterotaxy, visceral type 2 (HTX2).	Whole Blood 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 CFC1 gene"] Parameters [] Preparation ["No specific fasting required", "Inform lab of any relevant family history"] Indications ["Suspected Heterotaxy, visceral type 2", "Family history of HTX2", "Carrier testing", "Reproductive planning"] Measurement technique Confirm with laboratory Codes LOINC: 48000-4 ICD-10: Q89.8 Clinical summary This test evaluates the CFC1 gene for pathogenic variants associated with Heterotaxy, visceral type 2 (HTX2).
TEST-2973 CHD7 Gene CHARGE Syndrome Genetic Test This test evaluates the CHD7 gene for pathogenic variants associated with CHARGE syndrome.	Buccal Swab or Peripheral 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 the CHD7 gene", "Single nucleotide variants (SNVs)", "Small insertions and deletions (indels)"] Parameters [] Preparation ["No specific fasting required", "Inform lab of any recent blood transfusions (within 30 days)"] Indications ["Infants and children presenting with clinical features suggestive of CHARGE syndrome", "Carrier testing for parents of affected individuals"] Measurement technique Confirm with laboratory Codes LOINC: 96369-9 ICD-10: Q87.8 Clinical summary This test evaluates the CHD7 gene for pathogenic variants associated with CHARGE syndrome.
TEST-4606 CHRNG Gene Pterygium Syndrome Genetic Test This test analyzes the CHRNG gene to identify pathogenic variants associated with multiple pterygium syndrome.	Whole Blood, 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 ["Pathogenic variants in the CHRNG gene", "Single nucleotide variants", "Small insertions/deletions", "Copy number changes"] Parameters [] Preparation ["No fasting required", "Genetic counselling session required prior to sample collection"] Indications ["Individuals with suggestive clinical features", "Positive family history", "Carrier testing in at-risk relatives"] Measurement technique Confirm with laboratory Codes LOINC: 86214-6 ICD-10: Q87.89, Q79.8 Clinical summary This test analyzes the CHRNG gene to identify pathogenic variants associated with multiple pterygium syndrome.
TEST-4559 CIC Gene Intellectual Disability Nonsyndromic, CIC‑Related Genetic Test This test identifies pathogenic variants in the CIC gene, which are associated with nonsyndromic intellectual disability.	Whole blood (EDTA tube), 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 CIC gene", "Coding region of the CIC gene"] Parameters [] Preparation ["No fasting required", "Inform of any blood transfusions in the last three weeks", "Pre-test genetic counselling is mandatory"] Indications ["Suspected CIC-related nonsyndromic intellectual disability", "Unexplained developmental delay", "Family history of CIC-related disorders"] Measurement technique Confirm with laboratory Codes LOINC: 94048-7 ICD-10: F79 Clinical summary This test identifies pathogenic variants in the CIC gene, which are associated with nonsyndromic intellectual disability.
TEST-4360 CLCN2 Gene Epilepsy (Idiopathic Generalized Type 11) Test This genetic test evaluates the CLCN2 gene for pathogenic variants associated with Idiopathic Generalized Epilepsy Type 11 (IGE11).	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 the CLCN2 gene"] Parameters [] Preparation ["No specific fasting required", "Continue all prescribed anti-epileptic drugs"] Indications ["Diagnosis of Idiopathic Generalized Epilepsy Type 11 (IGE11)", "Family screening for IGE11"] Measurement technique Confirm with laboratory Codes LOINC: 81321-5 ICD-10: G40.3 Clinical summary This genetic test evaluates the CLCN2 gene for pathogenic variants associated with Idiopathic Generalized Epilepsy Type 11 (IGE11).
TEST-3748 CLCN5 Gene Hypophosphatemic Rickets Genetic Test This genetic test identifies pathogenic variants in the CLCN5 gene associated with Dent disease and X-linked hypophosphatemic rickets.	Whole Blood, Cheek Swab (Buccal), 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 CLCN5 gene", "Exons, splice junctions, and flanking intronic regions of CLCN5"] Parameters [] Preparation ["No specific fasting required", "Inform phlebotomist of all current medications"] Indications ["Children with vitamin-D-refractory rickets", "Individuals with hypercalciuria and low-molecular-weight proteinuria", "Patients with a family history suggestive of Dent disease", "Adults with unexplained kidney stones or early-onset chronic kidney disease"] Measurement technique Confirm with laboratory Codes LOINC: 94086-1 ICD-10: E83.31, N25.8 Clinical summary This genetic test identifies pathogenic variants in the CLCN5 gene associated with Dent disease and X-linked hypophosphatemic rickets.
TEST-4968 CLDN1 Gene (Ichthyosis, Leukocyte Vacuoles, Alopecia, Sclerosing Cholangitis) Genetic Test This genetic test detects pathogenic variants in the CLDN1 gene associated with the rare ILVASC syndrome.	Whole Blood, FTA Card, or Extracted DNA (Peripheral 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 the CLDN1 gene"] Parameters [] Preparation [] Indications ["Suspected ILVASC syndrome", "Familial variant screening", "Reproductive risk assessment"] Measurement technique Confirm with laboratory Codes LOINC: 48000-5 ICD-10: Q87.8 Clinical summary This genetic test detects pathogenic variants in the CLDN1 gene associated with the rare ILVASC syndrome.
TEST-4922 CLIC2 Gene X-Linked Intellectual Disability Type 32 Genetic Test (NGS) This genetic test identifies pathogenic variants in the CLIC2 gene associated with X-linked intellectual disability type 32.	Peripheral Whole Blood 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 CLIC2 gene", "Single-nucleotide variants", "Small insertion/deletion events"] Parameters [] Preparation [] Indications ["Suspected X-linked intellectual disability type 32", "Family history of CLIC2-related disorders"] Measurement technique Confirm with laboratory Codes LOINC: 51966-0 ICD-10: F78 Clinical summary This genetic test identifies pathogenic variants in the CLIC2 gene associated with X-linked intellectual disability type 32.

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.