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MPN Panel

Also referred as
Myeloproliferative Neoplasm Panel
For men & women
Earliest reports in
432 hours
Contains
3 tests
Test price:
₹19950
₹21000
5% off
Know more about this test
<font color='#864291'>Know more about this test</font>

The MPN Panel is a combination of genetic tests that detects mutations and gene fusions associated with myeloproliferative neoplasms (MPNs), a type of blood cancer. It helps doctors diagnose and classify MPNs, plan treatment, and monitor disease progression.

Samples required
Blood
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Why is this test booked?
Preparation for this test
Sample Collection
Who will collect your samples?
Test conducted by
Core Diagnostics Private Limited
ISO, CAP, NABL certified
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Know more about lab
Core Diagnostics Private Limited
ISO 9001:2015
ISO, CAP, NABL certified
About this lab
We at CORE Diagnostics are a renowned pathology testing laboratory & a premier institute in the country capable of providing varied diagnostic tests & facilities in the field of laboratory medicine and have established state-of-art testing facilities in Gurgaon. We are a Clinical laboratory focused on Next Generation Diagnostics for disease stratification and therapy selection. We are focused on bringing the most advanced testing techniques and expertise to India and aim to become the destination for all your high-end diagnostic needs.
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Understanding MPN Panel

Chronic myeloproliferative neoplasms (MPNs) are blood disorders in which the bone marrow produces too many red blood cells, white blood cells, or platelets. The MPN Panel is a comprehensive blood test test used to evaluate genetic changes in blood cells that are characteristic of myeloproliferative neoplasms.

The MPN Panel examines hotspot genes (specific regions of a gene that are frequently mutated), full genes (entire genes sequenced to detect rare or uncommon mutations), and gene fusions (abnormal joining of two genes that can drive disease). This comprehensive analysis is crucial for identifying specific types of myeloproliferative neoplasms (MPNs), including polycythemia vera (PV), essential thrombocythemia (ET), primary myelofibrosis (PMF), and for providing a broader genetic profile that helps in diagnosis and treatment planning.

Doctors may recommend the thi panel if you are experiencing symptoms such as fatigue, weakness, an enlarged spleen, or abnormal blood counts, or if you have a previously diagnosed MPN and need to monitor disease progression or treatment response. It is also advised for individuals with a family history of MPNs or known genetic risk factors. This test helps diagnose specific myeloproliferative neoplasms (MPNs), including chronic myeloid leukemia (CML), polycythemia vera (PV), essential thrombocythemia (ET), and primary myelofibrosis (PMF), differentiate between types of MPN for appropriate treatment, monitor response to therapy, and assess the risk of developing complications.

For this test, it is important to submit the clinical history, histopathology report, previous test results, and a doctor’s prescription at the time of sample collection. The Tata 1mg consolidated Test Requisition Form (TRF) must also be duly filled and submitted.

Lab test results may vary across different laboratories. Abnormal test results require an expert interpretation. Therefore, never try to self-medicate at home based solely on these results, and always consult a doctor for proper understanding of the test results.

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What does MPN Panel measure?

Contains 3 tests

The MPN Panel detects genetic mutations and gene fusions that are important in diagnosing and classifying myeloproliferative neoplasms (MPNs). The test is divided into the following categories:

Hotspot Genes: These genes are frequently mutated in MPNs and related blood disorders, and their analysis helps identify abnormal blood cell production:-

ABL1, CBL, FLT3, IDH1, IDH2, JAK2, KIT, MPL, NPM1, NRAS, SF3B1, SRSF2, U2AF1, DNMT3A

Full Genes: These genes are fully sequenced to detect a broader range of mutations, which can aid in disease classification, prognosis, and monitoring:

ASXL1, CALR, EZH2, IKZF1, NF1, RUNX1, SH2B3, STAG2, TET2, TP53, ZRSR2

Gene Fusions: Certain gene rearrangements (fusions) are analyzed because they can drive abnormal blood cell growth and impact disease behavior:-

ETV6, JAK2, KMT2A, RUNX1

By examining these hotspot genes, full genes, and gene fusions, the test provides a comprehensive molecular profile, helping doctors accurately diagnose, classify, and manage MPNs.

Hotspot genes: ABL1, CBL, FLT3, IDH1, IDH2, JAK2, KIT, MPL, NPM1, NRAS,SF3B1, SRSF2, U2AF1,DNMT3A
Full genes: ASXL1, CALR, EZH2, IKZF1, NF1, RUNX1, SH2B3, STAG2, TET2, TP53, ZRSR2
Gene Fusions: ETV6, JAK2, KMT2A ,RUNX1
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MPN Panel test price for other cities

Price inChennaiRs. 19950
Price inKolkataRs. 19950
Price inAllahabadRs. 19950
Price inBangaloreRs. 19950
Price inBhopalRs. 19950
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Easy online booking
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Live tracking of phlebotomist
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Safe Sample Collection
Safe Sample Collection
Our phlebotomists follow strict safety protocols to collect samples safely at home and on time.
Sample received at lab
Sample received at lab
Samples are transported securely to our accredited labs with world-class machines for testing by qualified experts.
Quick, Doctor-Verified Reports
Quick, Doctor-Verified Reports
Get doctor-approved reports via email and WhatsApp, with options for doctor follow-ups and AI insights.

FAQs related to MPN Panel

It is a genetic test that examines hotspot genes, full genes, and gene fusions associated with myeloproliferative neoplasms (MPNs), helping doctors diagnose, classify, and manage these blood disorders.
Individuals with persistently high blood counts; People suspected to have MPNs such as polycythemia vera (PV), essential thrombocythemia (ET), or primary myelofibrosis (PMF); Patients with a family history of MPNs or known genetic risk factors
A phlebotomist will clean your skin using an antiseptic alcohol cotton swab or wipe and take blood samples from your vein using a needle. The blood sample will be stored safely and transported to the laboratory for analysis.
No fasting is required for this test. You can schedule it at your convenience without avoiding food or water beforehand.
The test is generally safe. You may experience slight discomfort or bruising at the blood collection site, but serious complications are extremely rare.
Abnormal results indicate the presence of specific gene mutations or fusions associated with MPNs. Your doctor may use this information to diagnose the type of MPN, plan treatment, and monitor disease progression.
Symptoms may include fatigue, weakness, night sweats, headaches, weight loss, enlarged spleen, or blood clotting problems. Early stages may be asymptomatic and detected during routine blood tests.
There is currently no complete cure for most MPNs. Early diagnosis and treatment can control symptoms, prevent complications, and improve quality of life. Targeted therapies or bone marrow transplantation may be options depending on disease type and stage.
Recommended for everyone
This package is designed with everyone’s overall health considerations in mind, offering assessments to address a wide range of wellness needs.
Package can be booked by :
Men
Women
Contains 3 tests
Hotspot genes: ABL1, CBL, FLT3, IDH1, IDH2, JAK2, KIT, MPL, NPM1, NRAS,SF3B1, SRSF2, U2AF1,DNMT3A
Full genes: ASXL1, CALR, EZH2, IKZF1, NF1, RUNX1, SH2B3, STAG2, TET2, TP53, ZRSR2
Gene Fusions: ETV6, JAK2, KMT2A ,RUNX1
Report delivery
Standard time
432 hrs
For slots after 11 AM, report will be delivered in 432 hours.
Samples required
Blood
Our phlebotomist will draw a blood sample, typically from a vein in your inner elbow.
Preparations
1
Provide your clinical history, previous test reports, and a valid prescription. Tata 1mg consolidated TRF to be filled.
Why is this test booked?
1
If you have symptoms of MPN, such as fatigue, weakness, night sweats, or an enlarged spleen.
2
If your blood counts are abnormal or routine tests suggest a myeloproliferative disorder.
3
To monitor disease progression or response to treatment in previously diagnosed MPN patients.
4
If you have a family history of MPNs or known genetic risk factors.
5
To diagnose specific types of MPNs, such as polycythemia vera (PV), essential thrombocythemia (ET), or primary myelofibrosis (PMF).
6
To differentiate between MPN subtypes for appropriate treatment planning.
7
To assess the risk of developing complications associated with MPNs.
Who's behind your sample collection?
About Phlebotomist
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Certified Professionals
Certified & experienced professionals
Tata 1mg phlebotomists are DMLT / B.Sc MLT certified and have 1+ years of experience
Best collections
Best in-class collections
Tata 1mg phlebotomists are trained for painless, single-prick hygienic sample collection
Expertise
Comprehensive expertise
Other than sample collection, our phlebos are also skilled in first aid, ECG & BP monitoring
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