Test Price
2,800 AED✅ Home Collection Available
CDC20 Gene Cell Cycle Disorder Genetic Test in UAE | 2800 AED | DHA Licensed Lab
Executive Summary & Core Metrics
Clinical Precision & UAE Regulatory Assurance
- Accuracy Guarantee: 99.9% Diagnostic Sensitivity via ISO 9001:2015 Accredited Processing (Cert: INT/EGQ/2509DA/3139).
- Premium Logistics: VIP Mobile Phlebotomy & Temperature-Controlled Cold-Chain Home Collection, available daily from 8 AM to 11 PM.
- Clinical Guidance: Telephonic Post-Test Clinical Guidance in result interpretation with DHA-licensed genetics experts.
- Insurance Support: Direct Billing Verification via WhatsApp +971 54 548 8731.
Test Overview & Methodology
This next-generation sequencing (NGS) assay interrogates the entire coding region of the CDC20 gene, a pivotal mitotic checkpoint regulator, to detect single nucleotide variants, small indels, and copy number changes associated with oncogenesis and inherited cell cycle disorders.
Samples accepted: Peripheral whole blood, extracted DNA, or dried blood spot (FTA card). Turnaround time: 3–4 weeks.
| Feature | Our Test (DHA License #1143) | Closest Alternative |
|---|---|---|
| Precision | ≥30x depth, full gene NGS with CNV detection | Sanger sequencing of selected exons only |
| Methodology | NGS (Illumina NovaSeq) paired with bioinformatic pipeline | Capillary electrophoresis (Sanger) |
| Turnaround | 3–4 Weeks | 6–8 Weeks |
| UAE Compliance | DHA-licensed facility, ISO 9001:2015, PDPL compliant | Variable, often no local accreditation |
Physician Insight & Safety Protocols
“As a clinical geneticist, I view the CDC20 NGS result as one piece of a larger diagnostic puzzle. It should always be correlated with family history, histopathology, and other biomarkers. A negative result does not eliminate cancer risk, nor does a variant of uncertain significance warrant immediate intervention.” — Lina Osama Zaki Quteineh, Consultant Medical Genetics, DHA Registration ID: 9294403
⚠️ Medication Advisory
Do not discontinue any prescribed medication (e.g., chemotherapy, hormone therapy) or alter your treatment plan based solely on this genetic test outcome. Consult your oncologist or genetic counsellor for integrated clinical decision-making.
Pre-Test Exclusion Criteria
Do not proceed until resolved:
- Active febrile illness or systemic infection within 48 hours of sample collection.
- Recipient of allogeneic blood transfusion within the past 90 days (risk of DNA admixture).
- Inability to provide informed consent or absence of legal guardian for minors (per Federal Decree-Law No. 4 of 2016 on Medical Liability).
- Unwillingness to undergo mandatory pre‑test genetic counselling session to construct a pedigree chart.
Emergency Red Flags – seek immediate medical attention if you experience:
- Unexplained, rapid weight loss or persistent high fever during the testing window.
- Severe pain or bleeding at the venipuncture site that does not resolve within 20 minutes.
- Signs of anaphylaxis (swelling, difficulty breathing) after collection.
Patient FAQ & Clinical Guidance
1. What exactly does the CDC20 NGS test detect, and how does it influence cancer management?
The CDC20 NGS test detects pathogenic variants across the entire CDC20 gene, enabling oncologists to tailor surveillance protocols or select targeted therapies for cell cycle dysregulation cancers. It specifically identifies mutations linked to mitotic checkpoint failure, providing crucial data for hereditary cancer risk assessment in consenting adults under UAE Federal Decree-Law No. 4 of 2016 on Medical Liability.
2. Is home sample collection safe, and how is my genetic data protected under UAE law?
Our ISO-certified home collection uses a tamper-proof cold chain and is performed by DHA-licensed phlebotomists, while all genetic data is encrypted and stored within UAE borders in compliance with Federal Decree-Law No. 45 of 2021 on Personal Data Protection (PDPL) and Federal Law No. 2 of 2019 Concerning the Use of Information and Communication Technology in Health Fields. Your sample is de‑identified and handled solely for diagnostic purposes, never shared without explicit consent.
3. What if my CDC20 reveals a variant of uncertain significance (VUS)?
A VUS result means the laboratory identified a genetic change whose impact on protein function is not yet understood, and clinical correlation with your family pedigree and oncologist follow-up is essential to avoid overtreatment. We provide a complimentary telephonic consultation with a medical geneticist to explain the finding and recommend evidence‑based next steps.
UAE Regulatory & Data Privacy Adherence
Your Data Privacy and Health Information Protection
DNA Labs UAE operates under DHA Facility License 1143 and strictly adheres to Federal Decree-Law No. 45 of 2021 on Personal Data Protection (PDPL). All genetic and health data are encrypted, stored on secure UAE-based servers, and accessed only for diagnostic purposes. We also comply with Federal Law No. 2 of 2019 on the Use of Information and Communication Technology in Health Fields, ensuring that electronic health records remain confidential and are not shared without your written consent. Clinical safety and patient consent are governed by Federal Decree-Law No. 4 of 2016 on Medical Liability.
Clinical & Logistical Metadata
| Test Name | CDC20 Gene Cell Cycle Disorder Genetic Test |
| Price (AED) | 2800 |
| Turnaround Time | 3–4 Weeks |
| Sample Type / Matrix | Peripheral whole blood, extracted DNA, or dried blood spot (FTA card) |
| Methodology Used | Next-Generation Sequencing (NGS) on Illumina NovaSeq platform with bioinformatic analysis |
| ICD-10-CM Code | Z13.79 |
| LOINC Code | 21636-6 |
| DHA Facility License & Laboratory Address | DHA License #1143, Premises 105, Floor 1, Building 33, Dubai Healthcare City, Dubai, UAE – DNA Labs UAE |
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