Myeloid, unclear disease entity, NGS panel
Myeloische Erkrankung, Gesamtpanel NGSGensymbole
ALAS2 (Ex1-11), ANKRD26 (Ex1-34), ARID1A (Ex1-20), ASXL1 (Ex12), ASXL2 (Ex10-11), ATRX (Ex8-10 und 17-35), BCOR (Ex2-15), BCORL1 (Ex 1-12), BRAF (Ex 15), CALR (Ex9), CBL (Ex8-9), CBLB (Ex 9-10), CBLC (Ex7,8), CEBPA (Ex1), CSF3R (Ex14-17), CSMD1 (Ex 1-70), CSNK1A1 (Ex3-4), CUX1 (Ex1-24), DAXX (Ex1-8), DDX41 (Ex1-17), DHX15 (Ex3), DNMT3A (Ex2-23), ETNK1 (Ex1-8), ETV6 (Ex1-8), EZH2 (Ex2-17), FLT3 (Ex13-15 und 20), GATA1 (Ex2), GATA2 (Ex1-6), GNAS (Ex 8-9), HRAS (Ex2-5), IDH1 (Ex4), IDH2 (Ex4), IKZF1 (Ex2-8), JAK2 (12-15), JAK3 (Ex2-24), KDM6A (Ex1-29), KIT (Ex2,8-17), KRAS (Ex2-5), MPL(Ex4-12), NFE2 (Ex3-4), NPM1 (Ex11), NRAS (Ex2-5), PDGFRA (Ex12,14,18), PHF6 (Ex2-10), PIGA (Ex1-6), PPMD1 (Ex1-6), PTEN (Ex5,7), PTPN11 (Ex3,13), RAD21 (Ex2-14), RUNX1 (Ex2-9), SAMD9 (Ex3), SAMD9L (Ex5), SETBP1 (Ex4), SF1 (Ex1-13), SF3A1 (Ex1-16), SF3B1 (Ex13-15), SH2B3 (Ex2), SRP72 (Ex1-19), SRSF2 (Ex1), STAG1 (Ex2-34), STAG2 (Ex3-35), STAT3 Ex3,21), TET2 (Ex2-11), THPO (Ex1-6), TP53 (Ex2-11), U2AF1 (Ex2,6), U2AF2 (Ex1-12), UBA1 (Ex3), WT1 (Ex7, 9), ZBTB7A (Ex2,3), ZRSR2 (Ex1-11)
Siehe auch Tabelle Gen-Chromosom-Transkript-IDs des myeloischen Gesamtpanels.
Material
EDTA-Blut oder KM (EDTA bevorzugt): 1-2 ml
Methode
NGS
Kostenhinweis
EBM-Abrechnung möglich.
Indication
Markersuche bei V.a. noch unklare, myeloische Neoplasie. Sensitivität für MDS oder z.B. CMML > 90%.
Note
Literatur:
- Bejar et a., N Engl J Med 2011;364:2496-2506,
- Yoshida et al., Nature 2011 doi:10.1038/nature10496
- WHO Classification of Tumours of Haematopoietic and Lymphoid Tissues. WHO Classification of Tumours, Revised 4th Edition, Volume 2. Edited by Swerdlow SH, Campo E, Harris NL, Jaffe ES, Pileri SA, Stein H, Thiele J. 2017.
Contact person analyzes program
Dr. rer. nat. Thomas Haverkamp
Biologist Molecular Haemato-oncology, hereditary cancer syndromes- +49 231 9572-6617
- 0231 9572-86618