Universitätsklinikum Münster Institut für Genetik von Herzerkrankungen (IfGH)

85 capabilities Accredited since June 2026 Verified Oct 2026 One of 3,209 in Germany
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Albert-Schweitzer-Campus 1 Gebäude D3
Münster 48149 , Germany

Accreditation

Active DAkkS D-ML-13021-03-01
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Conducts molecular genetic testing for hereditary cardiac conditions, using PCR and Sanger sequencing on DNA extracted from EDTA blood samples to analyze genes such as ACTA2, ACTC1, and ANK2.

Accreditation Details

Accreditation Body

DAkkS

Number

D-ML-13021-03-01

Status

Active

Since

15 June 2026

Accreditation is granted under EU Regulation 765/2008 and assessed against ISO/IEC 17025. Data sourced from official DAkkS records.

Download Scope PDF

Additional scope documents

Download Scope PDF · D-ML-13021-03-00

Test Capabilities (85)
Standard Reference Description Category
10 mm vom Nennmaß des 10 mm vom Nennmaß des Dimensional / Geometric
ACTA2 ACTA2 Elemental Analysis
ACTC1 ACTC1 Elemental Analysis
ACTN2 ACTN2 Elemental Analysis
ANK2 ANK2 Elemental Analysis
C3 MYBPC3 Elemental Analysis
CACNA1C CACNA1C Elemental Analysis
CACNA1D CACNA1D Elemental Analysis
CACNA1S CACNA1S Elemental Analysis
CACNA2D1 CACNA2D1 Elemental Analysis
CACNB2 CACNB2 Elemental Analysis
CALM1 CALM1 Elemental Analysis
CALM2 CALM2 Elemental Analysis
CALM3 CALM3 Elemental Analysis
CASQ2 CASQ2 Elemental Analysis
CAV3 CAV3 Elemental Analysis
DCHS1 DCHS1 Elemental Analysis
DSC2 DSC2 Elemental Analysis
DSG2 DSG2 Elemental Analysis
GATA4 GATA4 Elemental Analysis
GPD1L GPD1L Elemental Analysis
HCN4 HCN4 Elemental Analysis
KCN12 KCN12 Elemental Analysis
KCNA5 KCNA5 Elemental Analysis
KCNE1 KCNE1 Elemental Analysis
KCNE2 KCNE2 Elemental Analysis
KCNE3 KCNE3 Elemental Analysis
KCNE5 KCNE5 Elemental Analysis
KCNH2 KCNH2 Elemental Analysis
KCNJ11 KCNJ11 Elemental Analysis
KCNJ5 KCNJ5 Elemental Analysis
KCNJ8 KCNJ8 Elemental Analysis
KCNQ1 KCNQ1 Elemental Analysis
LAMP2 LAMP2 Elemental Analysis
MYH6 MYH6 Elemental Analysis
MYH7 MYH7 Elemental Analysis
NKX2-5 NKX2-5 Elemental Analysis
PKP2 PKP2 Elemental Analysis
PRKAG2 PRKAG2 Elemental Analysis
PTPN11 PTPN11 Elemental Analysis
RBM20 RBM20 Elemental Analysis
RYR2 RYR2 Elemental Analysis
SCN1B SCN1B Elemental Analysis
SCN2B SCN2B Elemental Analysis
SCN3B SCN3B Elemental Analysis
SCN4B SCN4B Elemental Analysis
SCN5A SCN5A Elemental Analysis
SLC4A3 SLC4A3 Elemental Analysis
TGFBR1 TGFBR1 Elemental Analysis
TGFBR2 TGFBR2 Elemental Analysis
TMEM43 TMEM43 Elemental Analysis
TNNI3 TNNI3 Elemental Analysis
TNNT2 TNNT2 Elemental Analysis
TPM1 TPM1 Elemental Analysis
TRPM4 TRPM4 Elemental Analysis
Arrhythmogene Kardiomyopathie Arrhythmogene Kardiomyopathie Molecular Diagnostics / PCR
CYP2C19 OMIM*601130, CYP2C19 Molecular Diagnostics / PCR
DSP DSP Molecular Diagnostics / PCR
DTNA DTNA Molecular Diagnostics / PCR
Dilatative Kardiomyopathie (Panel- ID: DCM-V2): TTN, FLNC, LMNA, MYBPC3, MYH7, RBM20, SCN5A, TNNT2, TPM1, VCL, ACTC1, ACTN2, ANKRD1, BAG3, CDH2, CSRP3, DES, DSC2, DSG2, DSP, EMD, FHL1, JPH2, JUP, LAMP2, NEBL, NEXN, PLN, PSEN2, PTPN11, RAF1, RIT1, RYR2, SGCD, TMEM43, TMPO, TNNC1, TNNI3, ABCC9, CACNA1C, CTF1, DOLK, DTNA, EYA4, FKTN, GATA6, GLA, ILK, LAMA4, LDB3, MYH6, MYL2, NKX2-5, OBSCN, PLEKHM2, PRDM16, TBX20, TCAP, TNNI3K, RPL3L, KLF13, SLMAP, PPP1R13L, CRYAB, DMD, FKRP, MYPN, TAZ, TTR, DNAJB6 Dilatative Kardiomyopathie (Panel- ID: DCM-V2): TTN, FLNC, LMNA, MYBPC3, MYH7, RBM20, SCN5A, TNNT2, TPM1, VCL, ACTC1, ACTN2, ANKRD1, BAG3, CDH2, CSRP3, DES, DSC2, DSG2, DSP, EMD, FHL1, JPH2, JUP, LAMP2, NEBL, NEXN, PLN, PSEN2, PTPN11, RAF1, RIT1, RYR2, SGCD, TMEM43, TMPO, TNNC1, TNNI3, ABCC9, CACNA1C, CTF1, DOLK, DTNA, EYA4, FKTN, GATA6, GLA, ILK, LAMA4, LDB3, MYH6, MYL2, NKX2-5, OBSCN, PLEKHM2, PRDM16, TBX20, TCAP, TNNI3K, RPL3L, KLF13, SLMAP, PPP1R13L, CRYAB, DMD, FKRP, MYPN, TAZ, TTR, DNAJB6 Molecular Diagnostics / PCR
FLNA FLNA Molecular Diagnostics / PCR
FLNC FLNC Molecular Diagnostics / PCR
GLA GLA Molecular Diagnostics / PCR
Hypertrophe Kardiomyopathie- Panel (CMH/HCM, Panel ID: HCM- V2): ABCC9, ACTC1, ACTN2, ALPK3, ANKRD1, ATAD3A, BAG3, BRAF, CACNA1C, CALR3, CAV3, COX15, CRYAB, CSRP3, DES, FHL1, FHL2, FHOD3, FLNC, FXN, GAA, GLA, GYG1, HRAS, JPH2, KLHL24, KLF10, KRAS, LAMP2, LDB3, LZTR1, MAP2K1, MAP2K2, MYBPC3, MYH6, MYH7, MYL2, MYL3, MYLK2, MYOM1, MYOZ2, MYPN, NEXN, NRAS, OBSCN, PDLIM3, PLN, PRKAG2, PTPN11, RAF1, RASA2, RIT1, RRAS, RYR2, SHOC2, SLC25A4, SOS1, SOS2, TCAP, TNNC1, TNNI3, TNNT2, TPM1, TRIM63, TSFM, TTN, TTR, VCL, DNAJB6, MRAS, CBL, PPP1CB, SPRED1, NF1, RRAS2, VARS2, RIT1, AKT3, CCND2, EPHB4, PIK3CA, PIK3R2, RASA1, SASH1, SMARCB1, STAMBP, NNT, PLEKHM2 Hypertrophe Kardiomyopathie- Panel (CMH/HCM, Panel ID: HCM- V2): ABCC9, ACTC1, ACTN2, ALPK3, ANKRD1, ATAD3A, BAG3, BRAF, CACNA1C, CALR3, CAV3, COX15, CRYAB, CSRP3, DES, FHL1, FHL2, FHOD3, FLNC, FXN, GAA, GLA, GYG1, HRAS, JPH2, KLHL24, KLF10, KRAS, LAMP2, LDB3, LZTR1, MAP2K1, MAP2K2, MYBPC3, MYH6, MYH7, MYL2, MYL3, MYLK2, MYOM1, MYOZ2, MYPN, NEXN, NRAS, OBSCN, PDLIM3, PLN, PRKAG2, PTPN11, RAF1, RASA2, RIT1, RRAS, RYR2, SHOC2, SLC25A4, SOS1, SOS2, TCAP, TNNC1, TNNI3, TNNT2, TPM1, TRIM63, TSFM, TTN, TTR, VCL, DNAJB6, MRAS, CBL, PPP1CB, SPRED1, NF1, RRAS2, VARS2, RIT1, AKT3, CCND2, EPHB4, PIK3CA, PIK3R2, RASA1, SASH1, SMARCB1, STAMBP, NNT, PLEKHM2 Molecular Diagnostics / PCR
KCNJ2 KCNJ2 Molecular Diagnostics / PCR
Kammertachykardie (CPVT) (Panel- ID: CPVT-V2): RYR2, CASQ2, CALM1, CALM2, CALM3, TECRL, TRDN, KCNJ2, SCN5A Kammertachykardie (CPVT) (Panel- ID: CPVT-V2): RYR2, CASQ2, CALM1, CALM2, CALM3, TECRL, TRDN, KCNJ2, SCN5A Molecular Diagnostics / PCR
Katecholaminerge,polymorphe Katecholaminerge,polymorphe Molecular Diagnostics / PCR
LMNA LMNA Molecular Diagnostics / PCR
Langes QT Syndrom-Panel (LQTS; Panel-ID: LQTS-V2): CACNA1C, CALM1, CALM2, CALM3, CAV3, KCNE1, KCNH2, KCNJ2, KCNQ1, SCN5A, TECRL, TRDN Langes QT Syndrom-Panel (LQTS; Panel-ID: LQTS-V2): CACNA1C, CALM1, CALM2, CALM3, CAV3, KCNE1, KCNH2, KCNJ2, KCNQ1, SCN5A, TECRL, TRDN Molecular Diagnostics / PCR
Linksventrikuläre Non-Compaction Linksventrikuläre Noncompaction Molecular Diagnostics / PCR
PLN PLN Molecular Diagnostics / PCR
RRAD RRAD Molecular Diagnostics / PCR
Restriktive Kardiomyopathie (Panel- EDTA-Blut, DNA; DNA ID: RCM-V2): TAFAZZIN, MYBPC3, MYH7, MYL3, TNNI3, TTR, MYL2, TNNT2, TPM1, ACTN2, MYPN, TTN, FLNC, CRYAB, DES, BAG3, ACTC1, TNNC1, DCBLD2, LMNA, FHL1 Restriktive Kardiomyopathie (Panel- EDTA-Blut, DNA; DNA ID: RCM-V2): TAFAZZIN, MYBPC3, MYH7, MYL3, TNNI3, TTR, MYL2, TNNT2, TPM1, ACTN2, MYPN, TTN, FLNC, CRYAB, DES, BAG3, ACTC1, TNNC1, DCBLD2, LMNA, FHL1 Molecular Diagnostics / PCR
Sinusknotendysfunktion (SND), Vorhofflimmern (AFIB), progressive Sinusknotendysfunktion (SND), Vorhofflimmern (AFIB), progressive Molecular Diagnostics / PCR
TAZ TAZ Molecular Diagnostics / PCR
TECRL TECRL Molecular Diagnostics / PCR
TMEM168 TMEM168 Molecular Diagnostics / PCR
TRDN TRDN Molecular Diagnostics / PCR
TTR TTR Molecular Diagnostics / PCR
kardiale Reizleitungsstörung kardiale Reizleitungsstörung Molecular Diagnostics / PCR
(PCCD) (Panel-ID: SND_AFIB_PCCD- (PCCD) (Panel-ID: SND_AFIB_PCCD- Other
(Panel-ID: ACM-V2): PKP2, DSC2, (Panel-ID: ACM-V2): PKP2, DSC2, Other
Brugada-Syndrom (Panel-ID: BRU- Brugada-Syndrom (Panel-ID: BRU- Other
Kardiomyopathie (LVNC) (Panel-ID: Kardiomyopathie (LVNC) (Panel-ID: Other
Short QT Syndrom (Panel-ID: SQTS- Short QT Syndrom (Panel-ID: SQTS- Other

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