Erbil's Leading Genetics Lab

Precision Genetics for a Healthier Tomorrow

ImmunoGene Center delivers cutting-edge molecular diagnostics, next-generation sequencing, and personalized genetic testing from the heart of Erbil.

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A Specialized Genetics Laboratory in Erbil

ImmunoGene Center (IGC) is a premier medical genetics laboratory based in Erbil, Kurdistan Region, Iraq. We provide cutting-edge molecular diagnostics services — from next-generation sequencing and prenatal diagnosis to HLA typing and specialized PCR testing.

Our team of skilled geneticists and lab professionals is dedicated to delivering accurate and affordable results. Through collaborations with leading European institutions, we bring world-class diagnostics to the region.

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How It Works

Your journey from sample to results — simple and transparent

1📝

Test Request

Your physician orders the appropriate genetic test based on clinical need.

2🧪

Sample Collection

We collect the required sample (blood, tissue, or urine) at our lab.

3🔬

Lab Analysis

Advanced molecular testing using NGS, PCR, FISH, and Sanger sequencing.

4📋

Results Delivery

Receive a detailed, internationally formatted diagnostic report.

Our Services

Comprehensive molecular diagnostics powered by advanced technology

Next Generation Sequencing (NGS)

Whole exome, whole genome, and targeted panel sequencing for clinical and research applications.

Prenatal Diagnosis (PND)

Non-invasive and invasive prenatal testing to identify genetic conditions early during pregnancy.

DNA Sequencing

Sanger sequencing for targeted gene analysis, variant confirmation, and mutation detection.

PCR Testing

Real-time and conventional PCR for detecting pathogens, genetic markers, and DNA amplification.

MLPA Testing

Multiplex Ligation-dependent Probe Amplification for copy number variations, deletions, and duplications.

HLA Typing

High-resolution HLA typing for transplantation compatibility and disease association studies.

Molecular Infection Testing

Quantitative PCR for HBV, HCV, CMV, and BK virus detection and viral load monitoring.

Solid Organ Tumor Profiling

Somatic mutation panels for EGFR, ALK, ROS1, KRAS, BRAF, Her2, TP53, MSI, and more from FFPE tissue.

Molecular Hematology

Gene mutation analysis for AML, CLL, MDS, and MPN including FLT3, NPM1, IDH1/2, JAK2, and BCR-ABL.

FISH Testing

Fluorescence In Situ Hybridization for chromosomal deletions, translocations, and rearrangements.

Thrombophilia Screening

Factor V Leiden, MTHFR C677T, MTHFR A1298C, and B. Fibrinogen mutation testing.

Comprehensive Hematology Panels

Multi-gene panels for MPN, AML, ALL, CML, CLL, MDS, Eosinophilia, and Multiple Myeloma.

Test Menu & Pricing

Complete list of available tests with pricing in Iraqi Dinar (IQD)

Test Name	Sample Type	Price (IQD)
HBV	EDTA Tube	120,000
HCV	EDTA Tube	120,000
CMV	EDTA Tube	120,000
BK	Urine	120,000

Gene Name	Sample Type	Price (IQD)
MSI	FFPE (with histopathology report)	250,000
Kras-Braf-Nras	FFPE (with histopathology report)	250,000
PDGFRα	FFPE (with histopathology report)	250,000
RET Fusion	FFPE (with histopathology report)	250,000
TP53 Common Somatic Mutation	FFPE (with histopathology report)	250,000
EGFR Mutation (e18-21)	FFPE (with histopathology report)	220,000
Her2/NEU FISH	FFPE (with histopathology report)	300,000
MET Fusion	FFPE (with histopathology report)	250,000
ROS1 PCR	FFPE (with histopathology report)	250,000
ALK Common Somatic Mutation	FFPE (with histopathology report)	250,000
EML-ALK Fusion	FFPE (with histopathology report)	250,000
EGFR/ALK/ROS1 PCR	FFPE (with histopathology report)	250,000
GISTs Mutation Panel	FFPE (with histopathology report)	400,000
PDL-1	FFPE (with histopathology report)	250,000
MSI, Kras, Braf, Her2, MMR (MLH1, MLH2, MSH6, PMS2)	FFPE (with histopathology report)	950,000

Test Name	Sample Type	Price (IQD)
HLA Typing (A, B, DRB1)	EDTA Tube	175,000
HLA B27	EDTA Tube	100,000
HLA B51	EDTA Tube	100,000

Test Name	Sample Type	Price (IQD)
Factor V Leiden	EDTA Tube	100,000
MTHFR C677T	EDTA Tube	100,000
MTHFR A1298C	EDTA Tube	100,000
B. Fibrinogen	EDTA Tube	100,000

Test Name	Methodology	Price (IQD)
NPM1 Mutation Analysis	PCR & Sanger Sequencing	200,000
NPM1 mutations predict favorable prognosis in AML patients with normal karyotypes. This test examines exon 11 of the NPM1 gene, frequently co-occurring with FLT3 mutations.
FLT3 ITD/D835Y Mutation	PCR & Sanger Sequencing	200,000
FLT3 is the most commonly mutated gene in AML. ITD mutations (23% of AML) and D835 point mutations (8–12%) are assessed. ITD mutations are associated with poor prognosis.
IDH1/2 Mutation Analysis	PCR & Sanger Sequencing	250,000
IDH1/2 encode enzymes in glucose metabolism. Mutations at R132 (IDH1) and R140/R172 (IDH2) are biomarkers for glioma, AML, cholangiocarcinoma, and chondrosarcoma.
SRSF2 Mutation	PCR & Sanger Sequencing	250,000
SRSF2 mutations are observed in MDS, CLL, AML, and CMML. They cause abnormal expression patterns of genes involved in cancer pathogenesis.
GATA1 Mutation	PCR & Sanger Sequencing	250,000
GATA1 mutations are linked to Diamond-Blackfan anemia, acute megakaryoblastic leukemia, myeloproliferative disorders, and congenital dyserythropoietic anemias.
C.Kit Mutation	PCR & Sanger Sequencing	250,000
C-KIT mutations provide diagnostic, prognostic, and predictive information for systemic mastocytosis, GIST, melanoma, and AML.
ASXL1 Mutation	PCR & Sanger Sequencing	250,000
ASXL1 mutations are found in AML, MDS, MPN, and CMML. They are inversely associated with FLT3/NPM1 and confer higher chemotherapy resistance.
CEBPA Mutation	PCR & Sanger Sequencing	250,000
CEBPA mutations occur in 7–15% of AML patients and are associated with favorable prognosis in normal-karyotype AML without FLT3-ITD.
DNMT3A Mutation	PCR & Sanger Sequencing	250,000
DNMT3A mutations occur in ~20% of AML cases and are associated with altered DNA methylation patterns, rapid relapse, and poor survival.
U2AF1 Mutation	PCR & Sanger Sequencing	250,000
U2AF1 mutations are found in MDS, AML, and CMML. They are associated with poorer survival and occur at two mutational foci (S34 and Q157).
TP53 Mutation (Hematology)	PCR & Sanger Sequencing	250,000
TP53 mutations or 17p deletion indicate poor prognosis in CLL and other hematological malignancies, whether at initial diagnosis or during progression.
JAK2 V617F Mutation	RT-PCR	150,000
JAK2 Exon 12 Mutation	RT-PCR	150,000
CALR Mutation Analysis	RT-PCR	200,000
BCR-ABL1 p190 (Quantitative)	RT-PCR	150,000
BCR-ABL1 p210 (Quantitative)	RT-PCR	150,000
PML/RARA (Quantitative)	RT-PCR	250,000
ETV/RUNX1 Translocation (12;21)	RT-PCR	250,000
TCF3/PBX1 Translocation (1;19)	RT-PCR	250,000
t(8;21) Translocation	RT-PCR	250,000
CBFB/MYH11 inv(16) or t(16;16)	RT-PCR	250,000
Imatinib Resistance	PCR & Sanger Sequencing	250,000

Test Name	Methodology	Price (IQD)
Del 5q	FISH	250,000
Del 20q	FISH	250,000
Del 17q	FISH	250,000
IGH/CCND1 Translocation (11;14)	FISH	250,000
MYC Rearrangement	FISH	250,000
IGH/MYC t(8;14)	FISH	250,000
IGK Rearrangement	FISH	250,000
BCL Rearrangement	FISH	250,000
IGH/BCL2 t(14;18)	FISH	250,000

Panel Name	Includes	Price (IQD)
MPN Panel	JAK2 V617F, JAK2 Exon 12, CALR, MPL, C.Kit	250,000
AML Panel	Diagnostic: PML-RARA, AML1-ETO, Inv16 Prognostic: IDH1/2, FLT3 (ITD/D835Y), C.Kit	600,000
ALL Panel	BCR-ABL, t(12;21), t(1;19), t(4;11)	600,000
CML Panel	BCR-ABL p210 & p190	200,000
CLL Panel	11q del, Trisomy 12, 13q del, 17p del	450,000
MDS Panel	Chr Y loss, JAK2 V617F, Monosomy 7/7q del, Trisomy 8, 11q del/amp, 12p del, 17p del (TP53), 17q gain, Trisomy 19, 20q del, 3q del, 5q del	450,000
Eosinophilia Panel	PDGFRA, PDGFRB, PCM1-JAK2, FGFR1	450,000
Multiple Myeloma Panel	IGH/MYEOV t(11;14), IGH/MAF t(14;16), IGH/FGFR3 t(4;14), IGH/CCND3 t(6;14), IGH/MAFB t(14;20), 1p/12p/13q/14q/16q del, 1q/5q amp, Chr 9/15 gains, 17p del (TP53)	Contact for pricing

Why ImmunoGene?

What sets us apart as the region's trusted genetics partner

High Accuracy

NGS and PCR-based precision testing delivers highly accurate results, validated through rigorous quality control and international benchmarking standards.

Affordable Rates

Cost-effective pricing designed for the region, making advanced genetic diagnostics accessible to patients and healthcare providers alike.

Fast Turnaround

Rapid delivery of results, ensuring timely clinical decisions without compromising on depth or quality of analysis.

Dedicated Support

A responsive team available to assist physicians and patients with test selection, sample requirements, and report interpretation.

Local & International Collaboration

Partnered with top European institutions to bring world-class laboratory standards and expertise directly to the Kurdistan Region.

Frequently Asked Questions

Common questions about our genetic testing services

What samples do you need for testing?▼

Most tests require a simple blood draw (EDTA tube). Solid tumor tests need FFPE tissue blocks with a histopathology report. Some tests like BK virus accept urine samples. Our team will guide you on sample requirements when you place your order.

How do I prepare for a genetic test?▼

Most genetic tests require no special preparation — no fasting or diet changes needed. Simply visit our lab with a physician's referral or request during our working hours (2:30 PM – 7:30 PM).

Can I send samples from outside Erbil?▼

Yes, we accept samples from across Iraq and the region. Blood samples should be shipped in EDTA tubes at ambient temperature (stable for 3 days) or refrigerated (stable for 1 week). Contact us for shipping guidelines and courier arrangements.

Are your results accepted internationally?▼

Our laboratory follows international quality standards and collaborates with top European institutions. Our reports are detailed and follow standard formats recognized by clinicians and medical centers worldwide.

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Molecular Diagnostics

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NGS Certified

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EU Partnerships

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Quality Assured

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Clinical Grade

Get in Touch

We're here to answer your questions and help you get started

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Address

Erbil – Doctors Street – Talar Talaat Building – 2nd Floor, Apartment 19

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Phone

0751 140 4004
0783 207 4040

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Email

Immunogene2017@gmail.com

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Working Hours

Saturday – Thursday: 2:30 PM – 7:30 PM
Friday: Closed

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