Microgen Precision Dx - The future of Targeted Treatment

Explore All Tests

MicroGen Arrhythmogenic Right Ventricular Cardiomyopathy gene Panel

MHL Testcode : GG1
Methodology : NGS
Disease Segment : Cardiology
TAT : 26
Key genes :

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ACTN2 ✓
AKAP9 ✓
ANK2 ✓
ANKRD1 ✓
CACNA1C ✓
CACNB2 ✓
CASQ2 ✓
CAV3 ✓
CTNNA3 ✓
DES ✓
DSC2 ✓
DSG2 ✓
DSP ✓
EMD ✓
FLNC ✓
GPD1L ✓
HCN4 ✓
JUP ✓
KCNE1 ✓
KCNE2 ✓
KCNE3 ✓
KCNH2 ✓
KCNJ2 ✓
KCNJ5 ✓
KCNJ8 ✓
KCNQ1 ✓
LDB3 ✓
LMNA ✓
NKX2-5 ✓
PDLIM3 ✓
PKP2 ✓
PLN ✓
PRKAG2 ✓
RANGRF ✓
RBM20 ✓
RYR2 ✓
SCN1B ✓
SCN3B ✓
SCN4B ✓
SCN5A ✓
SNTA1 ✓
TGFB3 ✓
TMEM43 ✓
TNNI3 ✓
TNNT2 ✓
TTN ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Aorta gene Panel

MHL Testcode : GG2
Methodology : NGS
Disease Segment : Cardiology
TAT : 26
Key genes :

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ABCC6 ✓
ABL1 ✓
ACTA2 ✓
ADAMTS10 ✓
ADAMTS17 ✓
ADAMTS2 ✓
ADAMTSL4 ✓
ALDH18A1 ✓
BGN ✓
CBS ✓
COL1A1 ✓
COL1A2 ✓
COL2A1 ✓
COL3A1 ✓
COL5A1 ✓
COL5A2 ✓
EFEMP2 ✓
ELN ENPP1 ✓
FBLN5 ✓
FBN1 ✓
FBN2 ✓
FKBP14 ✓
FLNA ✓
GATA5 ✓
MAT2A ✓
MFAP5 ✓
MYH11 ✓
NOTCH1 ✓
PLOD1 ✓
SKI ✓
SLC2A10 ✓
SLC39A13 ✓
SMAD2 ✓
SMAD3 ✓
SMAD6 ✓
TGFB2 ✓
TGFB3 ✓
TGFBR1 ✓
TGFBR2 ✓
ZNF469 ✓
✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Arrhythmia gene Panel

MHL Testcode : GG3
Methodology : NGS
Disease Segment : Cardiology
TAT : 26
Key genes :

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ABCC9 ✓
ACTN2 ✓
AKAP9 ✓
ANK2 ✓
ANKRD1 ✓
CACNA1C ✓
CACNA2D1 ✓
CACNB2 ✓
CALM1 ✓
CALM2 ✓
CALM3 ✓
CASQ2 ✓
CAV3 ✓
CPT1A ✓
CTNNA3 ✓
DEPDC5 ✓
DES ✓
DSC2 ✓
DSG2 ✓
DSP ✓
EMD ✓
FLNC ✓
GJA5 ✓
GLA ✓
GPD1L ✓
GYG1 ✓
HCN4 ✓
JUP ✓
KCNA5 ✓
KCND3 ✓
KCNE1 ✓
KCNE2 ✓
KCNE3 ✓
KCNE5 ✓
KCNH2 ✓
KCNJ2 ✓
KCNJ5 ✓
KCNJ8 ✓
KCNK3 ✓
KCNQ1 ✓
KCNQ2 ✓
KCNQ3 ✓
KCNT1 ✓
LDB3 ✓
LMNA ✓
NKX2-5 ✓
NPPA ✓
PCDH19 ✓
PDLIM3 ✓
PKP2 ✓
PLN ✓
PRKAG2 ✓
PRRT2 ✓
RANGRF ✓
RBM20 ✓
RYR2 ✓
SCN10A ✓
SCN1A ✓
SCN1B ✓
SCN2B ✓
SCN3B ✓
SCN4B ✓
SCN5A ✓
SCN8A ✓
SCN9A ✓
SLC25A20 ✓
SLC2A1 ✓
SLMAP ✓
SNTA1 ✓
TBX5 ✓
TGFB3 ✓
TMEM43 ✓
TNNI3 ✓
TNNT2 ✓
TRDN ✓
TRPM4 ✓
TTN ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Atrial Fibrillation gene Panel

MHL Testcode : GG4
Methodology : NGS
Disease Segment : Cardiology
TAT : 26
Key genes :

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ABCC9 ✓
GJA5 ✓
HCN4 ✓
KCNA5 ✓
KCND3 ✓
KCNE1 ✓
KCNE2 ✓
KCNE5 ✓
KCNH2 ✓
KCNJ2 ✓
KCNQ1 ✓
MYL4 ✓
NPPA ✓
NUP155 ✓
SCN1B ✓
SCN2B ✓
SCN3B ✓
SCN4B ✓
SCN5A ✓
TNNI3K ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Brugada Syndrome gene Panel

MHL Testcode : GG5
Methodology : NGS
Disease Segment : Cardiology
TAT : 26
Key genes :

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×

ABCC9 ✓
GJA5 ✓
HCN4 ✓
KCNA5 ✓
KCND3 ✓
KCNE1 ✓
KCNE2 ✓
KCNE5 ✓
KCNH2 ✓
KCNJ2 ✓
KCNQ1 ✓
MYL4 ✓
NPPA ✓
NUP155 ✓
SCN1B ✓
SCN2B ✓
SCN3B ✓
SCN4B ✓
SCN5A ✓
TNNI3K ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Cardiac channelopathy gene panel

MHL Testcode : GG6
Methodology : NGS
Disease Segment : Cardiology
TAT : 26
Key genes :

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×

ABCC9 ✓
AKAP9 ✓
ALG10 ✓
ANK2 ✓
CACNA1C ✓
CACNA1D ✓
CACNA2D1 ✓
CACNB2 ✓
CALM1 ✓
CALM2 ✓
CASQ2 ✓
CAV3 ✓
DPP6 ✓
DSP ✓
FGF12 ✓
GATA4 ✓
GJA5 ✓
GNAI2 ✓
GPD1L ✓
HCN4 ✓
KCNA5 ✓
KCND2 ✓
KCND3 ✓
KCNE1 ✓
KCNE1L ✓
KCNE2 ✓
KCNE3 ✓
KCNH2 ✓
KCNJ2 ✓
KCNJ5 ✓
KCNJ8 ✓
KCNQ1 ✓
LMNA ✓
MIA3 ✓
NPPA ✓
NUP155 ✓
PKP2 ✓
RANGRF ✓
RYR2 ✓
SCN10A ✓
SCN1B ✓
SCN2B ✓
SCN3B ✓
SCN4B ✓
SCN5A ✓
SEMA3A ✓
SLMAP ✓
SNTA1 ✓
TRDN ✓
TRPM4 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Cardiomyopathy gene panel

MHL Testcode : GG7
Methodology : NGS
Disease Segment : Cardiology
TAT : 26
Key genes :

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×

AARS2 ✓
ABCC9 ✓
ACAD9 ✓
ACADVL ✓
ACTA1 ✓
ACTC1 ✓
ACTN2 ✓
AGK ✓
AGL ✓
ALMS1 ✓
ANK2 ✓
ANKRD1 ✓
ANO5 ✓
BAG3 ✓
BIN1 ✓
BRAF ✓
CALR3 ✓
CASQ2 ✓
CAV3 ✓
CFL2 ✓
CHKB ✓
CHRM2 ✓
COX15 ✓
CPT1A ✓
CPT2 ✓
CRYAB ✓
CSRP3 ✓
CTNNA3 ✓
DES ✓
DMD ✓
DNAJC19 ✓
DNM2 ✓
DOLK ✓
DPP6 ✓
DSC2 ✓
DSG2 ✓
DSG3 ✓
DSP ✓
DTNA ✓
DYSF ✓
EMD ✓
EYA4 ✓
FHL1 ✓
FHL2 ✓
FHOD3 ✓
FKTN ✓
FLNC ✓
FOXRED1 ✓
FXN ✓
GAA ✓
GATA4 ✓
GATAD1 ✓
GJA1 ✓
GJA5 ✓
GLA ✓
GLB1 ✓
GNE ✓
GUSB ✓
HCN4 ✓
HFE ✓
HRAS ✓
ILK ✓
ISCU ✓
JPH2 ✓
JUP ✓
KBTBD13 ✓
KCNA5 ✓
KCND3 ✓
KCNJ8 ✓
KLHL9 ✓
KRAS ✓
LAMA4 ✓
LAMP2 ✓
LDB3 ✓
LMNA ✓
LZTR1 ✓
MAP2K1 ✓
MAP2K2 ✓
MEGF10 ✓
MIB1 ✓
MSTN ✓
MTM1 ✓
MTO1 ✓
MYBPC1 ✓
MYBPC3 ✓
MYF6 ✓
MYH2 ✓
MYH6 ✓
MYH7 ✓
MYL2 ✓
MYL3 ✓
MYLK2 ✓
MYOT ✓
MYOZ2 ✓
MYPN ✓
NEB ✓
NEBL ✓
NEXN ✓
NF1 ✓
NOS1AP ✓
NPPA ✓
NRAS ✓
OBSCN ✓
PABPN1 ✓
PDLIM3 ✓
PKP2 ✓
PLEC ✓
PLN ✓
PRDM16 ✓
PRKAG2 ✓
PSEN1 ✓
PSEN2 ✓
PTPN11 ✓
PTRF ✓
RAF1 ✓
RANGRF ✓
RBM20 ✓
RIT1 ✓
RRAGC ✓
RYR2 ✓
SCN10A ✓
SCN5A ✓
SCNN1B ✓
SCNN1G ✓
SCO2 ✓
SDHA ✓
SEPN1 ✓
SGCD ✓
SGCG ✓
SHOC2 ✓
SLC22A5 ✓
SLC25A20 ✓
SLC25A4 ✓
SOS1 ✓
SRL ✓
TAZ ✓
TBX20 ✓
TBX5 ✓
TCAP ✓
TGFB3 ✓
TMEM43 ✓
TMEM70 ✓
TMPO ✓
TNNC1 ✓
TNNI3 ✓
TNNI3K ✓
TNNT2 ✓
TPM1 ✓
TSFM ✓
TTN ✓
TTR ✓
VCL ✓
VCP ✓
XK ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Cardiomyopathy predisposition - MYBPC3

MHL Testcode : GG8
Methodology : PCR
Disease Segment : Cardiology
TAT : 26
Key genes :

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MYBC3 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Catecholaminergic Polymorphic Ventricular Tachycardia Panel

MHL Testcode : GG9
Methodology : NGS
Disease Segment : Cardiology
TAT : 26
Key genes :

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ANK2 ✓
CALM1 ✓
CALM2 ✓
CALM3 ✓
CASQ2 ✓
KCNJ2 ✓
KCNQ1 ✓
RYR2 ✓
SCN5A ✓
TECRL ✓
TRDN ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Comprehensive Cardiology gene Panel

MHL Testcode : GG10
Methodology : NGS
Disease Segment : Cardiology
TAT : 26
Key genes :

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AARS2 ✓
ABCC6 ✓
ABCC9 ✓
ACAD9 ✓
ACADVL ✓
ACTA1 ✓
ACTA2 ✓
ACTC1 ✓
ACTN2 ✓
AGK ✓
AGL ✓
AKAP9 ✓
ALMS1 ✓
ALPK3 ✓
ANK2 ✓
ANO5 ✓
APOA1 ✓
BAG3 ✓
BRAF ✓
CACNA1C ✓
CACNA2D1 ✓
CACNB2 ✓
CALM1 ✓
CALM2 ✓
CALM3 ✓
CALR3 ✓
CAPN3 ✓
CASQ2 ✓
CAV3 ✓
CBL ✓
CDH2 ✓
COX15 ✓
CPT2 ✓
CRPPA ✓
CRYAB ✓
CSRP3 ✓
CTNNA3 ✓
DBH ✓
DES ✓
DMD ✓
DNAJC19 ✓
DOLK ✓
DSC2 ✓
DSG2 ✓
DSP ✓
DTNA ✓
DYSF ✓
EEF1A2 ✓
ELAC2 ✓
EMD ✓
ENPP1 ✓
EPG5 ✓
ETFA ✓
ETFB ✓
ETFDH ✓
FBXO32 ✓
FHL1 ✓
FKRP ✓
FKTN ✓
FLNC ✓
FOXD4 ✓
FOXRED1 ✓
FXN ✓
GAA ✓
GATA5 ✓
GATA6 ✓
GATAD1 ✓
GBE1 ✓
GFM1 ✓
GLA ✓
GLB1 ✓
GMPPB ✓
GTPBP3 ✓
GUSB ✓
HADHA ✓
HAND1 ✓
HCN4 ✓
HFE ✓
HRAS ✓
JPH2 ✓
JUP ✓
KCNA5 ✓
KCNE1 ✓
KCNE2 ✓
KCNH2 ✓
KCNJ2 ✓
KCNJ5 ✓
KCNQ1 ✓
KRAS ✓
LAMA2 ✓
LAMP2 ✓
LARGE1 ✓
LDB3 ✓
LMNA ✓
LRRC10 ✓
LZTR1 ✓
MAP2K1 ✓
MAP2K2 ✓
MLYCD ✓
MTO1 ✓
MYBPC3 ✓
MYBPHL ✓
MYH6 ✓
MYH7 ✓
MYL2 ✓
MYL3 ✓
MYL4 ✓
MYOT ✓
MYPN ✓
NDUFAF2 ✓
NEXN ✓
NF1 ✓
NKX2-5 ✓
NOS1AP ✓
NRAS ✓
NUP155 ✓
PCCA ✓
PCCB ✓
PKP2 ✓
PLEC ✓
PLEKHM2 ✓
PLN ✓
PNPLA2 ✓
POMT1 ✓
PPA2 ✓
PPP1CB ✓
PRDM16 ✓
PRKAG2 ✓
PTPN11 ✓
RAF1 ✓
RASA2 ✓
RBCK1 ✓
RBM20 ✓
RIT1 ✓
RMND1 ✓
RRAS ✓
RYR2 ✓
SALL4 ✓
SCN10A ✓
SCN1B ✓
SCN3B ✓
SCN5A ✓
SCNN1B ✓
SCNN1G ✓
SCO2 ✓
SDHA ✓
SELENON ✓
SGCA ✓
SGCB ✓
SGCD ✓
SGCG ✓
SHOC2 ✓
SLC22A5 ✓
SLC25A20 ✓
SLC25A4 ✓
SMCHD1 ✓
SOS1 ✓
SOS2 ✓
SPEG ✓
SPRED1 ✓
TAB2 ✓
TAFAZZIN ✓
TBX20 ✓
TBX5 ✓
TCAP ✓
TECRL ✓
TGFB3 ✓
TMEM43 ✓
TMEM70 ✓
TNNC1 ✓
TNNI3 ✓
TNNI3K ✓
TNNT2 ✓
TOR1AIP1 ✓
TPM1 ✓
TRDN ✓
TRIM32 ✓
TRPM4 ✓
TSFM ✓
TTN ✓
TTR ✓
VCL ✓
VCP ✓
VPS13A ✓
XK ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Congenital Structural Heart Disease gene Panel

MHL Testcode : GG11
Methodology : NGS
Disease Segment : Cardiology
TAT : 26
Key genes :

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ACTC1 ✓
ACVR2B ✓
AKT3 ✓
ALMS1 ✓
ARL6 ✓
ARMC4 ✓
B9D1 ✓
B9D2 ✓
BBS1 ✓
BBS10 ✓
BBS12 ✓
BBS2 ✓
BBS4 ✓
BBS5 ✓
BBS7 ✓
BBS9 ✓
BCOR ✓
BRAF ✓
CBL ✓
CC2D2A ✓
CCDC103 ✓
CCDC114 ✓
CCDC151 ✓
CCDC28B ✓
CCDC39 ✓
CCDC40 ✓
CCDC65 ✓
CCNO ✓
CEP290 ✓
CFAP298 ✓
CFAP53 ✓
CHD7 ✓
CITED2 ✓
CPS1 ✓
CRELD1 ✓
CYR61 ✓
DNAAF1 ✓
DNAAF2 ✓
DNAAF3 ✓
DNAAF4 ✓
DNAAF5 ✓
DNAH11 ✓
DNAH5 ✓
DNAH8 ✓
DNAI1 ✓
DNAI2 ✓
DNAL1 ✓
DRC1 ✓
DTNA ✓
ELN ✓
FLNA ✓
FOXF1 ✓
FOXH1 ✓
GATA4 ✓
GATA6 ✓
GDF1 ✓
GJA1 ✓
GPC3 ✓
HAND1 ✓
HRAS ✓
INVS ✓
JAG1 ✓
KIF7 ✓
KRAS ✓
LEFTY2 ✓
MAP2K1 ✓
MAP2K2 ✓
MCIDAS ✓
MED13L ✓
MKKS ✓
MKS1 ✓
MMP21 ✓
MYH6 ✓
NEK8 ✓
NKX2-5 ✓
NKX2-6 ✓
NME8 ✓
NODAL ✓
NOTCH1 ✓
NPHP3 ✓
NR2F2 ✓
NRAS ✓
NSD1 ✓
NTRK3 ✓
OFD1 ✓
PIK3CA ✓
PIK3R2 ✓
PITX2 ✓
PKD1L1 ✓
PTPN11 ✓
RAF1 ✓
RAI1 ✓
RBM10 ✓
RIT1 ✓
RPGRIP1L ✓
SEMA3E ✓
SHOC2 ✓
SMAD6 ✓
SOS1 ✓
SPAG1 ✓
TAB2 ✓
TBX1 ✓
TBX20 ✓
TBX5 ✓
TCTN2 ✓
TLL1 ✓
TMEM216 ✓
TMEM231 ✓
TMEM67 ✓
TRIM32 ✓
TTC8 ✓
WDPCP ✓
ZFPM2 ✓
ZIC3 ✓
ZMYND10 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Connective tissue disorder gene panel

MHL Testcode : GG12
Methodology : NGS
Disease Segment : Cardiology
TAT : 26
Key genes :

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×

ABCC6 ✓
ACTA2 ✓
ACVR1 ✓
ADAMTS2 ✓
ADAMTSL2 ✓
AEBP1 ✓
ALDH18A1 ✓
ALPL ✓
ATP6AP1 ✓
ATP6V0A2 ✓
ATP6V1A ✓
ATP6V1E1 ✓
ATP7A ✓
B3GALT6 ✓
B3GAT3 ✓
B4GALT7 ✓
BGN ✓
BPNT2 ✓
C1R ✓
C1S ✓
CBS ✓
CHD4 ✓
CHST14 ✓
CHST3 ✓
COL11A1 ✓
COL11A2 ✓
COL12A1 ✓
COL1A1 ✓
COL1A2 ✓
COL2A1 ✓
COL3A1 ✓
COL5A1 ✓
COL5A2 ✓
COL6A2 ✓
COL6A3 ✓
COL9A1 ✓
COL9A2 ✓
COL9A3 ✓
CRTAP ✓
CSGALNACT1 ✓
DCHS1 ✓
DSE ✓
EFEMP2 ✓
ELN ✓
ERBIN ✓
FBLN5 ✓
FBN1 ✓
FBN2 ✓
FKBP14 ✓
FLCN ✓
FLNA ✓
FLNB ✓
FOXE3 ✓
GGCX ✓
GORAB ✓
KIF22 ✓
LOX ✓
LOXL3 ✓
LRP2 ✓
LTBP3 ✓
LTBP4 ✓
LZTS1 ✓
MAT2A ✓
MED12 ✓
MFAP5 ✓
MOCS1 ✓
MYH11 ✓
MYLK ✓
NEK9 ✓
NEPRO ✓
NOTCH1 ✓
NT5E ✓
P3H1 ✓
P4HA1 ✓
PLOD1 ✓
PLOD3 ✓
PLP1 ✓
PRDM5 ✓
PRKG1 ✓
PYCR1 ✓
RIN2 ✓
ROBO3 ✓
ROCK2 ✓
SERPING1 ✓
SHOC2 ✓
SKI ✓
SLC2A10 ✓
SLC39A13 ✓
SMAD2 ✓
SMAD3 ✓
SMAD4 ✓
SMS ✓
SPARC ✓
TGFB2 ✓
TGFB3 ✓
TGFBR1 ✓
TGFBR2 ✓
TNFRSF1A ✓
TNXB ✓
VCAN ✓
ZNF469 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Coronary artery disease Polygenic Risk Test

MHL Testcode : GG13
Methodology : Microarray
Disease Segment : Cardiology
TAT : 18
Key genes :

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NA ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Cutis-laxa gene panel

MHL Testcode : GG14
Methodology : NGS
Disease Segment : Cardiology
TAT : 26
Key genes :

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ALDH18A1 ✓
ATP6V0A2 ✓
ATP6V1A ✓
ATP6V1E1 ✓
ATP7A ✓
EFEMP2 ✓
ELN ✓
FBLN5 ✓
GORAB ✓
LTBP4 ✓
PYCR1 ✓
RIN2 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen CYP2C19 Clopidogrel resistance

MHL Testcode : GG15
Methodology : NGS
Disease Segment : Cardiology
TAT : 26
Key genes :

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×

CYP2C19 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Dilated Cardiomyopathy gene Panel

MHL Testcode : GG16
Methodology : NGS
Disease Segment : Cardiology
TAT : 26
Key genes :

+ Show Genes

×

ABCC6 ✓
ABCC9 ✓
ACTA1 ✓
ACTC1 ✓
ACTN2 ✓
ALMS1 ✓
ALPK3 ✓
APOA1 ✓
BAG3 ✓
DES ✓
DMD ✓
DOLK ✓
DSC2 ✓
DSG2 ✓
DSP ✓
DYSF ✓
EEF1A2 ✓
EMD ✓
EPG5 ✓
ETFA ✓
ETFB ✓
ETFDH ✓
FBXO32 ✓
FKTN ✓
FLNC ✓
FOXD4 ✓
GATA6 ✓
GATAD2A ✓
GBE1 ✓
GLB1 ✓
HAND1 ✓
HCN4 ✓
JPH2 ✓
JUP ✓
LAMP2 ✓
LMNA ✓
LRRC10 ✓
MLYCD ✓
MYBPC3 ✓
MYBPHL ✓
MYH6 ✓
MYH7 ✓
MYL4 ✓
PCCA ✓
PCCB ✓
PKP2 ✓
PLEKHM2 ✓
PLN ✓
PRDM16 ✓
RAF1 ✓
RBCK1 ✓
RBM20 ✓
RMND1 ✓
SCN5A ✓
SPEG ✓
TAB2 ✓
TAFAZZIN ✓
TBX20 ✓
TBX5 ✓
TCAP ✓
TNNC1 ✓
TNNI3 ✓
TNNI3K ✓
TNNT2 ✓
TOR1AIP1 ✓
TPM1 ✓
TTN ✓
TTR ✓
VCL ✓
VPS13A ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Ehler Danlos syndrome gene panel

MHL Testcode : GG17
Methodology : NGS
Disease Segment : Cardiology
TAT : 26
Key genes :

+ Show Genes

×

ABCC6 ✓
ACTA2 ✓
ADAMTS2 ✓
ADAMTSL2 ✓
AEBP1 ✓
ALDH18A1 ✓
ATP6AP1 ✓
ATP6V0A2 ✓
ATP6V1A ✓
ATP6V1E1 ✓
ATP7A ✓
B3GALT6 ✓
B3GAT3 ✓
B4GALT7 ✓
BGN ✓
C1R ✓
C1S ✓
CBS ✓
CHST14 ✓
CHST3 ✓
COL11A1 ✓
COL12A1 ✓
COL1A1 ✓
COL1A2 ✓
COL2A1 ✓
COL3A1 ✓
COL5A1 ✓
COL5A2 ✓
COL6A2 ✓
COL6A3 ✓
CRTAP ✓
DSE ✓
EFEMP2 ✓
ELN ✓
FBLN5 ✓
FBN1 ✓
FBN2 ✓
FKBP14 ✓
FLNA ✓
FLNB ✓
GGCX ✓
GORAB ✓
LOX ✓
LTBP4 ✓
LZTS1 ✓
MOCS1 ✓
P3H1 ✓
PLOD1 ✓
PLP1 ✓
PRDM5 ✓
PYCR1 ✓
RIN2 ✓
ROBO3 ✓
SKI ✓
SLC39A13 ✓
SMAD2 ✓
SMAD3 ✓
SPARC ✓
TGFB2 ✓
TGFB3 ✓
TGFBR1 ✓
TGFBR2 ✓
TNFRSF1A ✓
TNXB ✓
ZNF469 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Ehlers-Danlos syndrome type VI deletion/duplication analysis

MHL Testcode : GG18
Methodology : MLPA
Disease Segment : Cardiology
TAT : 26
Key genes :

+ Show Genes

×

PLOD1 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Fibrodysplasia ossificans progressive gene sequencing

MHL Testcode : GG19
Methodology : NGS
Disease Segment : Cardiology
TAT : 26
Key genes :

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×

ACVR1 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen GDF1 and PKD1L1 gene sequencing

MHL Testcode : GG20
Methodology : NGS
Disease Segment : Cardiology
TAT : 26
Key genes :

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×

GDF1 and PKD1L1 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Hereditary Hemorrhagic Telangiectasia gene Panel

MHL Testcode : GG21
Methodology : NGS
Disease Segment : Cardiology
TAT : 26
Key genes :

+ Show Genes

×

ACVRL1 ✓
ENG ✓
EPHB4 ✓
GDF2 ✓
RASA1 ✓
SMAD4 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Hereditary Transthyretin-mediated amyloidosis TTR gene analysis

MHL Testcode : GG22
Methodology : NGS
Disease Segment : Cardiology
TAT : 26
Key genes :

+ Show Genes

×

TTR ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Heterotaxy and Situs Inversus gene Panel

MHL Testcode : GG23
Methodology : NGS
Disease Segment : Cardiology
TAT : 26
Key genes :

+ Show Genes

×

ACVR2B ✓
AK7 ✓
ANKS6 ✓
CCDC103 ✓
CCDC39 ✓
CCDC40 ✓
CFAP298 ✓
CFAP300 ✓
CFAP53 ✓
DNAAF1 ✓
DNAAF11 ✓
DNAAF2 ✓
DNAAF3 ✓
DNAAF4 ✓
DNAAF5 ✓
DNAAF6 ✓
DNAH1 ✓
DNAH11 ✓
DNAH5 ✓
DNAH6 ✓
DNAH9 ✓
DNAI1 ✓
DNAI2 ✓
DNAL1 ✓
FOXH1 ✓
FOXJ1 ✓
GAS2L2 ✓
GAS8 ✓
GDF1 ✓
HYDIN ✓
INVS ✓
LEFTY2 ✓
LRRC56 ✓
MMP21 ✓
NKX2-5 ✓
NME8 ✓
NODAL ✓
ODAD1 ✓
ODAD2 ✓
ODAD3 ✓
ODAD4 ✓
OFD1 ✓
PKD1L1 ✓
SMAD2 ✓
SPAG1 ✓
TTC12 ✓
ZIC3 ✓
ZMYND10 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Hypercholesterolemia gene panel

MHL Testcode : GG24
Methodology : NGS
Disease Segment : Cardiology
TAT : 26
Key genes :

+ Show Genes

×

APOB ✓
LDLR ✓
LDLRAP1 ✓
PCSK9 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Hyperlipidemia gene Panel

MHL Testcode : GG25
Methodology : NGS
Disease Segment : Cardiology
TAT : 26
Key genes :

+ Show Genes

×

ABCA1 ✓
ABCG5 ✓
ABCG8 ✓
APOA1 ✓
APOB ✓
APOC3 ✓
APOE ✓
LDLR ✓
LDLRAP1 ✓
LPL ✓
PCSK9 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Hypertrophic Cardiomyopathy gene Panel

MHL Testcode : GG26
Methodology : NGS
Disease Segment : Cardiology
TAT : 26
Key genes :

+ Show Genes

×

ACADVL ✓
ACTC1 ✓
ACTN2 ✓
AGL ✓
ALPK3 ✓
BAG3 ✓
BRAF ✓
CACNA1C ✓
CAV3 ✓
CBL ✓
CPT2 ✓
CSRP3 ✓
DES ✓
ELAC2 ✓
FHL1 ✓
FHOD3 ✓
FLNC ✓
GAA ✓
GLA ✓
HRAS ✓
JPH2 ✓
KLHL24 ✓
KRAS ✓
LAMP2 ✓
LDB3 ✓
LZTR1 ✓
MAP2K1 ✓
MAP2K2 ✓
MRAS ✓
MTO1 ✓
MYBPC3 ✓
MYH6 ✓
MYH7 ✓
MYL2 ✓
MYL3 ✓
MYLK2 ✓
MYOZ2 ✓
MYPN ✓
NEXN ✓
NF1 ✓
NRAS ✓
PLN ✓
PPP1CB ✓
PRKAG2 ✓
PTPN11 ✓
RAF1 ✓
RASA2 ✓
RIT1 ✓
RRAS ✓
SHOC2 ✓
SOS1 ✓
SOS2 ✓
TANGO2 ✓
TCAP ✓
TNNC1 ✓
TNNI3 ✓
TNNT2 ✓
TPM1 ✓
TTR ✓
VCL ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Left Ventricular Non-Compaction Cardiomyopathy gene Panel

MHL Testcode : GG27
Methodology : NGS
Disease Segment : Cardiology
TAT : 26
Key genes :

+ Show Genes

×

ABCC9 ✓
BAG3 ✓
CTNNA3 ✓
DES ✓
DMD ✓
DSC2 ✓
DSG2 ✓
DSP ✓
DTNA ✓
EMD ✓
FBXO32 ✓
FLNC ✓
HCN4 ✓
JPH2 ✓
JUP ✓
LAMP2 ✓
LMNA ✓
MIPEP ✓
MYBPC3 ✓
MYH6 ✓
MYH7 ✓
PKP2 ✓
PLEKHM2 ✓
PLN ✓
RAF1 ✓
RBM20 ✓
RYR2 ✓
SCN5A ✓
TCAP ✓
TNNT2 ✓
TPM1 ✓
TTN* ✓
VCL ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Liddle Syndrome gene Panel

MHL Testcode : GG28
Methodology : NGS
Disease Segment : Cardiology
TAT : 26
Key genes :

+ Show Genes

×

SCNN1B ✓
SCNN1G ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Long QT Syndrome gene Panel

MHL Testcode : GG29
Methodology : NGS
Disease Segment : Cardiology
TAT : 26
Key genes :

+ Show Genes

×

AKAP9 ✓
ANK2 ✓
CACNA1C ✓
CALM1 ✓
CALM2 ✓
CALM3 ✓
CAV3 ✓
KCNE1 ✓
KCNE2 ✓
KCNH2 ✓
KCNJ2 ✓
KCNJ5 ✓
KCNQ1 ✓
SCN4B ✓
SCN5A ✓
SNTA1 ✓
TANGO2 ✓
TECRL ✓
TRDN ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Marfan syndrome gene analysis

MHL Testcode : GG30
Methodology : NGS
Disease Segment : Cardiology
TAT : 26
Key genes :

+ Show Genes

×

FBN1 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Marfan Syndrome gene Panel

MHL Testcode : GG31
Methodology : NGS
Disease Segment : Cardiology
TAT : 26
Key genes :

+ Show Genes

×

ABL1 ✓
ADAMTS10 ✓
ADAMTS17 ✓
ADAMTSL4 ✓
BGN ✓
CBS ✓
COL11A1 ✓
COL11A2 ✓
COL1A1 ✓
COL1A2 ✓
COL2A1 ✓
COL3A1 ✓
COL5A1 ✓
COL5A2 ✓
EFEMP2 ✓
FBN1 ✓
FBN2 ✓
MAT2A ✓
MED12 ✓
PLOD1 ✓
SKI ✓
SLC2A10 ✓
SMAD3 ✓
SMAD6 ✓
TGFB2 ✓
TGFB3 ✓
TGFBR1 ✓
TGFBR2 ✓
UPF3B ✓
VCAN ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Noonan and RASopathies gene panel

MHL Testcode : GG32
Methodology : NGS
Disease Segment : Cardiology
TAT : 26
Key genes :

+ Show Genes

×

A2ML1 ✓
ACTB ✓
ACTG1 ✓
BRAF ✓
CBL ✓
CCNK ✓
CDC42 ✓
EPHB4 ✓
FGD1 ✓
HRAS ✓
KAT6B ✓
KRAS ✓
LZTR1 ✓
MAP2K1 ✓
MAP2K2 ✓
MAP3K8 ✓
MRAS ✓
NF1 ✓
NRAS ✓
PPP1CB ✓
PTPN11 ✓
RAF1 ✓
RASA1 ✓
RASA2 ✓
RIT1 ✓
RRAS ✓
SASH1 ✓
SHOC2 ✓
SOS1 ✓
SOS2 ✓
SPRED1 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Pulmonary Artery Hypertension gene Panel

MHL Testcode : GG33
Methodology : NGS
Disease Segment : Cardiology
TAT : 26
Key genes :

+ Show Genes

×

ACVRL1 ✓
BMPR2 ✓
CAV1 ✓
EIF2AK4 ✓
ENG ✓
FOXF1 ✓
KCNA5 ✓
KCNK3 ✓
NFU1 ✓
RASA1 ✓
SMAD4 ✓
TBX4 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Short QT Syndrome gene Panel

MHL Testcode : GG34
Methodology : NGS
Disease Segment : Cardiology
TAT : 26
Key genes :

+ Show Genes

×

CACNA1C ✓
CACNA2D1 ✓
CACNB2 ✓
KCNH2 ✓
KCNJ2 ✓
KCNQ1 ✓
SLC4A3 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen SHOX deletion/duplication analysis

MHL Testcode : GG35
Methodology : MLPA
Disease Segment : Cardiology
TAT : 26
Key genes :

+ Show Genes

×

SHOX ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroPlex Clopidogrel dosage CYP2C192 & CYP2C193

MHL Testcode : GG36
Methodology : RTPCR
Disease Segment : Cardiology
TAT : 12
Key genes :

+ Show Genes

×

CYP2C19*2 ✓
CYP2C19*3 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroPlex Statin induced myopathy predisposition SLCO1B1 p.(Val174Ala)

MHL Testcode : GG37
Methodology : RTPCR
Disease Segment : Cardiology
TAT : 12
Key genes :

+ Show Genes

×

SLCO1B1 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroPlex Tangier Disease gene sequencing

MHL Testcode : GG38
Methodology : NGS
Disease Segment : Cardiology
TAT : 26
Key genes :

+ Show Genes

×

ABCA1 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroPlex Warfarin dosage-VKORC1 , CYP2C92,CYP2C93

MHL Testcode : GG39
Methodology : RTPCR
Disease Segment : Cardiology
TAT : 12
Key genes :

+ Show Genes

×

VKORC1 ✓
CYP2C9*2 ✓
CYP2C9*3 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Acute intermittent porphyria - HMBS gene analysis

MHL Testcode : GG195
Methodology : NGS
Disease Segment : Dermatology
TAT : 28
Key genes :

+ Show Genes

×

HMBS ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Adams-Oliver Syndrome gene panel

MHL Testcode : GG196
Methodology : NGS
Disease Segment : Dermatology
TAT : 28
Key genes :

+ Show Genes

×

ARHGAP31 ✓
DLL4 ✓
DOCK6 ✓
EOGT ✓
KCTD1 ✓
MYH9 ✓
NOTCH1 ✓
RBPJ ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Albinism gene panel

MHL Testcode : GG197
Methodology : NGS
Disease Segment : Dermatology
TAT : 28
Key genes :

+ Show Genes

×

AP3B1 ✓
AP3D1 ✓
BLOC1S3 ✓
BLOC1S6 ✓
DTNBP1 ✓
EDN3 ✓
EDNRB ✓
GPR143 ✓
HPS1 ✓
HPS3 ✓
HPS4 ✓
HPS5 ✓
HPS6 ✓
KIT ✓
LRMDA ✓
LYST ✓
MC1R ✓
MITF ✓
MLPH ✓
MYO5A ✓
OCA2 ✓
PAX3 ✓
RAB27A ✓
SLC24A5 ✓
SLC45A2 ✓
SNAI2 ✓
SOX10 ✓
TYR ✓
TYRP1 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen ATP2A2 gene sequencing

MHL Testcode : GG198
Methodology : NGS
Disease Segment : Dermatology
TAT : 28
Key genes :

+ Show Genes

×

ATP2A2 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Cutis Laxa gene panel

MHL Testcode : GG199
Methodology : NGS
Disease Segment : Dermatology
TAT : 28
Key genes :

+ Show Genes

×

ALDH18A1 ✓
ATP6V0A2 ✓
ATP7A ✓
EFEMP2 ✓
ELN ✓
FBLN5 ✓
GORAB ✓
LTBP4 ✓
PYCR1 ✓
SLC2A10 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Dyskeratosis Congenita gene panel

MHL Testcode : GG200
Methodology : NGS
Disease Segment : Dermatology
TAT : 28
Key genes :

+ Show Genes

×

ACD ✓
AK2 ✓
CTC1 ✓
DKC1 ✓
NAF1 ✓
NHP2 ✓
NOP10 ✓
PARN ✓
POT1 ✓
RTEL1 ✓
TERC ✓
TERT ✓
TINF2 ✓
USB1 ✓
WRAP53 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Ectodermal dysplasia gene panel

MHL Testcode : GG201
Methodology : NGS
Disease Segment : Dermatology
TAT : 28
Key genes :

+ Show Genes

×

BCS1L ✓
CDH3 ✓
DSP ✓
EDA ✓
EDAR ✓
EDARADD ✓
ERCC2 ✓
EVC ✓
EVC2 ✓
GJB2 ✓
GJB6 ✓
HOXC13 ✓
HR ✓
IFT122* ✓
JUP ✓
LRP6 ✓
MPLKIP ✓
PAX9 ✓
PORCN ✓
PRKD1 ✓
PVRL4 ✓
RMRP ✓
TP63 ✓
WDR35 ✓
WNT10A ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen EDA, EDAR, EDARADD gene analysis

MHL Testcode : GG202
Methodology : MLPA
Disease Segment : Dermatology
TAT : 21
Key genes :

+ Show Genes

×

EDA ✓
EDAR ✓
EDARADD ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Ehlers-Danlos Syndrome gene panel

MHL Testcode : GG203
Methodology : NGS
Disease Segment : Dermatology
TAT : 28
Key genes :

+ Show Genes

×

ABCC6 ✓
ACTA2 ✓
ADAMTS2 ✓
ADAMTSL2 ✓
AEBP1 ✓
ALDH18A1 ✓
ATP6AP1 ✓
ATP6V0A2 ✓
ATP6V1A ✓
ATP6V1E1 ✓
ATP7A ✓
B3GALT6 ✓
B3GAT3 ✓
B4GALT7 ✓
BGN ✓
C1R ✓
C1S ✓
CBS ✓
CHST14 ✓
CHST3 ✓
COL11A1 ✓
COL12A1 ✓
COL1A1 ✓
COL1A2 ✓
COL2A1 ✓
COL3A1 ✓
COL5A1 ✓
COL5A2 ✓
COL6A2 ✓
COL6A3 ✓
CRTAP ✓
DSE ✓
EFEMP2 ✓
ELN ✓
FBLN5 ✓
FBN1 ✓
FBN2 ✓
FKBP14 ✓
FLNA ✓
FLNB ✓
GGCX ✓
GORAB ✓
LOX ✓
LTBP4 ✓
LZTS1 ✓
MOCS1 ✓
P3H1 ✓
PLOD1 ✓
PLP1 ✓
PRDM5 ✓
PYCR1 ✓
RIN2 ✓
ROBO3 ✓
SKI ✓
SLC39A13 ✓
SMAD2 ✓
SMAD3 ✓
SPARC ✓
TGFB2 ✓
TGFB3 ✓
TGFBR1 ✓
TGFBR2 ✓
TNFRSF1A ✓
TNXB ✓
ZNF469 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Epidermolysis bullosa gene panel

MHL Testcode : GG204
Methodology : NGS
Disease Segment : Dermatology
TAT : 28
Key genes :

+ Show Genes

×

CD151 ✓
COL17A1 ✓
COL7A1 ✓
DSP ✓
DST ✓
EXPH5 ✓
FERMT1 ✓
ITGA3 ✓
ITGA6 ✓
ITGB4 ✓
KRT14 ✓
KRT5 ✓
LAMA3 ✓
LAMB3 ✓
LAMC2 ✓
MMP1 ✓
PKP1 ✓
PLEC ✓
TGM5 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Erythropoietic protoporphyria-1 (FECH) gene sequencing

MHL Testcode : GG205
Methodology : NGS
Disease Segment : Dermatology
TAT : 28
Key genes :

+ Show Genes

×

FECH ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Harlequin ichthyosis (ABCA12) gene analysis

MHL Testcode : GG206
Methodology : NGS
Disease Segment : Dermatology
TAT : 28
Key genes :

+ Show Genes

×

ABCA12 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Hereditary Acrodermatitis Enteropathica gene panel

MHL Testcode : GG207
Methodology : NGS
Disease Segment : Dermatology
TAT : 28
Key genes :

+ Show Genes

×

SLC30A2 ✓
SLC39A4 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Hereditary Melanoma and Skin Cancer gene panel

MHL Testcode : GG208
Methodology : NGS
Disease Segment : Dermatology
TAT : 28
Key genes :

+ Show Genes

×

BAP1 ✓
BRCA1 ✓
BRCA2 ✓
CDK4 ✓
CDKN2A ✓
DDB2 ✓
ERCC2 ✓
ERCC3 ✓
ERCC4 ✓
ERCC5 ✓
MITF ✓
POT1 ✓
PTCH1 ✓
PTEN ✓
SUFU ✓
TP53 ✓
WRN ✓
XPA ✓
XPC ✓
✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Hermansky-Pudlak Syndrome gene panel

MHL Testcode : GG209
Methodology : NGS
Disease Segment : Dermatology
TAT : 28
Key genes :

+ Show Genes

×

ABCA3 ✓
AP3B1 ✓
AP3D1 ✓
BLOC1S3 ✓
BLOC1S6 ✓
DKC1 ✓
DTNBP1 ✓
GPR143 ✓
HPS1 ✓
HPS3 ✓
HPS4 ✓
HPS5 ✓
HPS6 ✓
LYST ✓
OCA2 ✓
SFTPB ✓
SFTPC ✓
SLC45A2 ✓
TERC ✓
TERT ✓
TINF2 ✓
TYR ✓
TYRP1 ✓
✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Ichthyosis gene panel

MHL Testcode : GG210
Methodology : NGS
Disease Segment : Dermatology
TAT : 28
Key genes :

+ Show Genes

×

ABCA12 ✓
ABHD5 ✓
ALDH3A2 ✓
ALOX12B ✓
ALOXE3 ✓
AP1S1 ✓
CASP14 ✓
CDSN ✓
CERS3 ✓
CLDN1 ✓
CSTA ✓
CYP4F22 ✓
DSG1 ✓
DSP ✓
EBP ✓
FLG ✓
GJB2 ✓
GJB3 ✓
GJB4 ✓
KRT1 ✓
KRT10 ✓
KRT2 ✓
LIPN ✓
LOR ✓
NIPAL4 ✓
PHGDH ✓
PHYH ✓
PNPLA1 ✓
POMP ✓
PSAT1 ✓
SLC27A4 ✓
SLURP1 ✓
SNAP29 ✓
SPINK5 ✓
ST14 ✓
STS ✓
TGM1 ✓
TGM5 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Kindler syndrome (FERMT1) gene sequencing

MHL Testcode : GG211
Methodology : NGS
Disease Segment : Dermatology
TAT : 28
Key genes :

+ Show Genes

×

FERMT1 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen KRT5 gene sequencing

MHL Testcode : GG212
Methodology : NGS
Disease Segment : Dermatology
TAT : 28
Key genes :

+ Show Genes

×

KRT5 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Neurofibromatosis gene panel

MHL Testcode : GG213
Methodology : NGS
Disease Segment : Dermatology
TAT : 28
Key genes :

+ Show Genes

×

KIT ✓
KITLG ✓
LZTR1 ✓
NF1* ✓
NF2 ✓
PTPN11 ✓
RAF1 ✓
SMARCB1 ✓
SPRED1 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Pachyonychia Congenita gene panel

MHL Testcode : GG214
Methodology : NGS
Disease Segment : Dermatology
TAT : 28
Key genes :

+ Show Genes

×

AAGAB ✓
CRYL1 ✓
GJB6 ✓
KRT16 ✓
KRT17 ✓
KRT6A ✓
KRT6B ✓
KRT6C ✓
TRPV3 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Palmoplantar Keratoderma gene panel

MHL Testcode : GG215
Methodology : NGS
Disease Segment : Dermatology
TAT : 28
Key genes :

+ Show Genes

×

AAGAB ✓
AQP5 ✓
CAST ✓
COL14A1 ✓
CRYL1 ✓
CTSC ✓
DSG1 ✓
DSP ✓
ENPP1 ✓
FAM83G ✓
GJB2 ✓
GJB4 ✓
GJB6 ✓
JUP ✓
KRT1 ✓
KRT14 ✓
KRT16 ✓
KRT17 ✓
KRT6A ✓
KRT6B ✓
KRT6C ✓
KRT9 ✓
LOR ✓
MBTPS2 ✓
PKP1 ✓
POMP ✓
RHBDF2 ✓
RSPO1 ✓
SERPINB7 ✓
SLURP1 ✓
SMARCAD1 ✓
SNAP29 ✓
TAT ✓
TRPV3 ✓
VPS33B ✓
WNT10A ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen PLEC gene sequencing

MHL Testcode : GG216
Methodology : NGS
Disease Segment : Dermatology
TAT : 28
Key genes :

+ Show Genes

×

PLEC ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Progeria and Progeroid Syndromes gene panel

MHL Testcode : GG217
Methodology : NGS
Disease Segment : Dermatology
TAT : 28
Key genes :

+ Show Genes

×

AGPAT2 ✓
ALDH18A1 ✓
B4GALT7 ✓
BLM ✓
BSCL2 ✓
COL3A1 ✓
ERCC2 ✓
ERCC4 ✓
ERCC5 ✓
ERCC6 ✓
ERCC8 ✓
GORAB ✓
LMNA ✓
PYCR1 ✓
RECQL4 ✓
WRN ✓
ZMPSTE24 ✓
✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Sjogren-Larsson syndrome (ALDH3A2) gene analysis

MHL Testcode : GG218
Methodology : NGS
Disease Segment : Dermatology
TAT : 28
Key genes :

+ Show Genes

×

ALDH3A2 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Tuberous Sclerosis gene panel

MHL Testcode : GG219
Methodology : NGS
Disease Segment : Dermatology
TAT : 28
Key genes :

+ Show Genes

×

TSC1 ✓
TSC2 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen TYR deletion/duplication analysis

MHL Testcode : GG220
Methodology : NGS
Disease Segment : Dermatology
TAT : 28
Key genes :

+ Show Genes

×

TYR ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Waardenburg Syndrome gene panel

MHL Testcode : GG221
Methodology : NGS
Disease Segment : Dermatology
TAT : 28
Key genes :

+ Show Genes

×

EDN3 ✓
EDNRB ✓
MITF ✓
KIT ✓
PAX3 ✓
SNAI2 ✓
SOX10 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Xeroderma pigmentosum gene panel

MHL Testcode : GG222
Methodology : NGS
Disease Segment : Dermatology
TAT : 28
Key genes :

+ Show Genes

×

DDB2 ✓
ERCC2 ✓
ERCC3 ✓
ERCC4 ✓
ERCC5 ✓
POLH ✓
XPA ✓
XPC ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen ZMPSTE24 gene sequencing

MHL Testcode : GG223
Methodology : NGS
Disease Segment : Dermatology
TAT : 28
Key genes :

+ Show Genes

×

ZMPSTE24 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen 4H syndrome gene panel

MHL Testcode : GG40
Methodology : NGS
Disease Segment : Neurology
TAT : 28
Key genes :

+ Show Genes

×

POLR3A ✓
POLR3B ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen ABCD1 gene analysis

MHL Testcode : GG41
Methodology : NGS
Disease Segment : Neurology
TAT : 28
Key genes :

+ Show Genes

×

ABCD1 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen ADGRG1 gene sequencing

MHL Testcode : GG42
Methodology : NGS
Disease Segment : Neurology
TAT : 28
Key genes :

+ Show Genes

×

ADGRG1 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Adrenoleukodystrophy , gene analysis

MHL Testcode : GG43
Methodology : NGS
Disease Segment : Neurology
TAT : 28
Key genes :

+ Show Genes

×

ABCD1 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen ADSSL1 gene analysis

MHL Testcode : GG44
Methodology : NGS
Disease Segment : Neurology
TAT : 28
Key genes :

+ Show Genes

×

ADSSL1 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Aicardi-Goutieres syndrome gene panel

MHL Testcode : GG45
Methodology : NGS
Disease Segment : Neurology
TAT : 28
Key genes :

+ Show Genes

×

ADAR ✓
IFIH1 ✓
RNASEH2A ✓
RNASEH2B ✓
RNASEH2C ✓
SAMHD1 ✓
TREX1 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Alexander disease , gene analysis

MHL Testcode : GG46
Methodology : NGS
Disease Segment : Neurology
TAT : 28
Key genes :

+ Show Genes

×

GFAP ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Alkaptonuria , gene analysis

MHL Testcode : GG47
Methodology : NGS
Disease Segment : Neurology
TAT : 28
Key genes :

+ Show Genes

×

HGD ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Amyotrophic Lateral Sclerosis gene panel

MHL Testcode : GG48
Methodology : NGS
Disease Segment : Neurology
TAT : 28
Key genes :

+ Show Genes

×

ANG ✓
ANXA11 ✓
APOE ✓
ARHGEF28 ✓
ATXN2 ✓
C9orf72 ✓
CFAP410 ✓
CHCHD10 ✓
CHMP2B ✓
DCTN1 ✓
ERBB4 ✓
FIG4 ✓
FUS ✓
HNRNPA1 ✓
HNRNPA2B1 ✓
KIF5A ✓
MATR3 ✓
MOBP ✓
NEFH ✓
NEK1 ✓
OPTN ✓
PFN1 ✓
SETX ✓
SOD1 ✓
SQSTM1 ✓
TAF15 ✓
TARDBP ✓
TBK1 ✓
TUBA4A ✓
UBQLN2 ✓
UNC13A ✓
VAPB ✓
VCP ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Arthrogryposis and congenital myasthenic syndrome gene panel

MHL Testcode : GG49
Methodology : NGS
Disease Segment : Neurology
TAT : 28
Key genes :

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ADCY6 ✓
ADGRG6 ✓
AGRN ✓
ALG14 ✓
ALG2 ✓
CHAT ✓
CHRNA1 ✓
CHRNB1 ✓
CHRND ✓
CHRNE ✓
CHRNG ✓
CHST14 ✓
CNTNAP1 ✓
COL13A1 ✓
COLQ ✓
DNM2 ✓
DOK7 ✓
DPAGT1 ✓
ECEL1 ✓
ERBB3 ✓
FBN2 ✓
GFPT1 ✓
GLE1 ✓
LAMB2 ✓
LRP4 ✓
MUSK ✓
MYBPC1 ✓
MYH3 ✓
MYH8 ✓
NALCN ✓
PI4KA ✓
PIEZO2 ✓
PIP5K1C ✓
RAPSN ✓
SCN4A ✓
SLC18A3 ✓
SLC35A3 ✓
SNAP25 ✓
SYT2 ✓
TNNI2 ✓
TNNT3 ✓
TPM2 ✓
UBA1 ✓
VIPAS39 ✓
VPS33B ✓
ZBTB42 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Ataxia-telangiectasia , deletion and duplication analysis

MHL Testcode : GG50
Methodology : MLPA
Disease Segment : Neurology
TAT : 21
Key genes :

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×

ATM ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Ataxia-telangiectasia , gene analysis

MHL Testcode : GG51
Methodology : NGS
Disease Segment : Neurology
TAT : 28
Key genes :

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×

ATM ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen ATP1A2 and ATP1A3 gene sequencing

MHL Testcode : GG52
Methodology : NGS
Disease Segment : Neurology
TAT : 28
Key genes :

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×

ATP1A2 and ATP1A3 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen ATRX gene analysis

MHL Testcode : GG53
Methodology : NGS
Disease Segment : Neurology
TAT : 28
Key genes :

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×

ATRX ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Autism Spectrum Disorders gene panel ,

MHL Testcode : GG54
Methodology : NGS
Disease Segment : Neurology
TAT : 28
Key genes :

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×

ACTB ✓
ADNP ✓
ADSL ✓
AHDC1 ✓
ALDH5A1 ✓
ANK2 ✓
ANK3 ✓
ANKRD11 ✓
ARHGEF9 ✓
ARID1B ✓
ARX ✓
ASH1L ✓
ASXL3 ✓
AUTS2 ✓
BAZ2B ✓
BCKDK ✓
BCL11A ✓
BRAF ✓
BRSK2 ✓
C12orf57 ✓
CACNA1C ✓
CACNA2D3 ✓
CASK ✓
CC2D1A ✓
CDC42BPB ✓
CDKL5 ✓
CHAMP1 ✓
CHD2 ✓
CHD3 ✓
CHD7 ✓
CHD8 ✓
CIC ✓
CNOT3 ✓
CNTN6 ✓
CNTNAP2 ✓
CREBBP ✓
CSDE1 ✓
CTCF ✓
CTNND2 ✓
CTTNBP2 ✓
CUL3 ✓
DDX3X ✓
DEAF1 ✓
DHCR7 ✓
DISC1 ✓
DLG4 ✓
DNMT3A ✓
DSCAM ✓
DYRK1A ✓
EBF3 ✓
EFR3A ✓
EHMT1 ✓
EP300 ✓
FMR1 ✓
FOXG1 ✓
FOXP1 ✓
FOXP2 ✓
GABRB3 ✓
GAMT ✓
GATM ✓
GIGYF1 ✓
GRIN2B ✓
GRIP1 ✓
HCN1 ✓
HIVEP2 ✓
HNRNPH2 ✓
HNRNPU ✓
HRAS ✓
IQSEC2 ✓
IRF2BPL ✓
KANSL1 ✓
KATNAL2 ✓
KCNB1 ✓
KCNQ3 ✓
KDM3B ✓
KDM5B ✓
KDM6B ✓
KMT2A ✓
KMT2C ✓
KMT2E ✓
KMT5B ✓
KRAS ✓
MAGEL2 ✓
MAOA ✓
MBD5 ✓
MBOAT7 ✓
MECP2 ✓
MED13 ✓
MED13L ✓
MEIS2 ✓
MYT1L ✓
NAA15 ✓
NACC1 ✓
NBEA ✓
NDP ✓
NEXMIF ✓
NFIX ✓
NLGN3 ✓
NLGN4X ✓
NR4A2 ✓
NRXN1 ✓
NRXN3 ✓
NSD1 ✓
PACS1 ✓
PCDH19 ✓
PHF21A ✓
PHF3 ✓
POGZ ✓
POMGNT1 ✓
PPP1CB ✓
PPP2R5D ✓
PQBP1 ✓
PRR12 ✓
PSMD12 ✓
PTCHD1 ✓
PTEN ✓
PTPN11 ✓
RAB39B ✓
RAD21 ✓
RAF1 ✓
RAI1 ✓
RELN ✓
RERE ✓
RFX3 ✓
SCN1A ✓
SCN2A ✓
SCN8A ✓
SETBP1 ✓
SETD2 ✓
SETD5 ✓
SGSH ✓
SHANK2 ✓
SHANK3 ✓
SIN3A ✓
SLC6A1 ✓
SLC9A6 ✓
SMAD4 ✓
SMARCC2 ✓
SON ✓
SOX5 ✓
SPAST ✓
STXBP1 ✓
STXBP5 ✓
SYNGAP1 ✓
TANC2 ✓
TAOK1 ✓
TBC1D20 ✓
TBCK ✓
TBL1XR1 ✓
TBR1 ✓
TCF20 ✓
TCF4 ✓
TLK2 ✓
TNRC6B ✓
TRAF7 ✓
TRIO ✓
TRIP12 ✓
TSC1 ✓
TSC2 ✓
TSHZ3 ✓
UBE3A ✓
UPF3B ✓
VPS13B ✓
WAC ✓
WDFY3 ✓
ZBTB20 ✓
ZMYND11 ✓
ZNF292 ✓
ZNF407 ✓
ZNF462 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Autosomal dominant adult-onset demyelinating leukodystrophy , deletion and duplication analysis

MHL Testcode : GG55
Methodology : MLPA
Disease Segment : Neurology
TAT : 21
Key genes :

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×

LMNB1 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Benign infantile epilepsy gene panel

MHL Testcode : GG56
Methodology : NGS
Disease Segment : Neurology
TAT : 28
Key genes :

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×

CHRNA2 ✓
KCNQ2 ✓
KCNQ3 ✓
PRRT2 ✓
SCN2A ✓
SCN8A ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Comprehensive Epilepsy gene Panel

MHL Testcode : GG57
Methodology : NGS
Disease Segment : Neurology
TAT : 28
Key genes :

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×

AARS ✓
AARS2 ✓
ABAT ✓
ABCC8 ✓
ABHD16A ✓
ACOX1 ✓
ACTB ✓
ACTG1 ✓
ACTL6B ✓
ACY1 ✓
ADAM22 ✓
ADAR ✓
ADARB1 ✓
ADAT3 ✓
ADCY5 ✓
ADGRG1 ✓
ADGRL1 ✓
ADGRV1 ✓
ADNP ✓
ADPRHL2 ✓
ADRA2B ✓
ADSL ✓
AFDN ✓
AFF3 ✓
AFG3L2 ✓
AGA ✓
AGMO ✓
AGO1 ✓
AHDC1 ✓
AHI1 ✓
AIMP1 ✓
AKT1 ✓
AKT3 ✓
ALDH3A2 ✓
ALDH4A1 ✓
ALDH5A1 ✓
ALDH7A1 ✓
ALG1 ✓
ALG11 ✓
ALG12 ✓
ALG13 ✓
ALG14 ✓
ALG2 ✓
ALG3 ✓
ALG6 ✓
ALG8 ✓
ALG9 ✓
ALKBH8 ✓
ALPL ✓
AMACR ✓
AMPD2 ✓
AMT ✓
ANK3 ✓
ANKRD11 ✓
ANKRD17 ✓
AP1G1 ✓
AP2M1 ✓
AP3B2 ✓
AP3D1 ✓
AP4B1 ✓
AP4M1 ✓
APC2 ✓
ARF1 ✓
ARFGEF1 ✓
ARFGEF2 ✓
ARG1 ✓
ARHGEF15 ✓
ARHGEF9 ✓
ARID1A ✓
ARID1B ✓
ARL13B ✓
ARSA ✓
ARSB ✓
ARV1 ✓
ARX ✓
ASAH1 ✓
ASH1L ✓
ASNS ✓
ASPA ✓
ASPM ✓
ASTN1 ✓
ASXL2 ✓
ASXL3 ✓
ATAD1 ✓
ATIC ✓
ATN1 ✓
ATP13A2 ✓
ATP1A1 ✓
ATP1A2 ✓
ATP1A3 ✓
ATP2A2 ✓
ATP2B1 ✓
ATP5F1A ✓
ATP5F1E ✓
ATP5MC3 ✓
ATP5PO ✓
ATP6AP2 ✓
ATP6V0A1 ✓
ATP6V0A2 ✓
ATP6V0C ✓
ATP6V1A ✓
ATP6V1B2 ✓
ATP7A ✓
ATPAF2 ✓
ATRX ✓
AUH ✓
AUTS2 ✓
B3GALNT2 ✓
B4GALT1 ✓
B4GAT1 ✓
BAP1 ✓
BCAS3 ✓
BCKDHA ✓
BCKDHB ✓
BCKDK ✓
BCL11A ✓
BCS1L ✓
BICD2 ✓
BOLA3 ✓
BPTF ✓
BRAF ✓
BRAT1 ✓
BRD2 ✓
BSCL2 ✓
BTD ✓
BUB1B ✓
C12orf57 ✓
C19orf12 ✓
C2orf69 ✓
CACNA1A ✓
CACNA1B ✓
CACNA1C ✓
CACNA1D ✓
CACNA1E ✓
CACNA1G ✓
CACNA1H ✓
CACNA1I ✓
CACNA2D1 ✓
CACNA2D2 ✓
CACNB4 ✓
CAD ✓
CAMK2A ✓
CAMK2B ✓
CAMSAP1 ✓
CAMTA1 ✓
CAPRIN1 ✓
CARS2 ✓
CASK ✓
CASR ✓
CBL ✓
CC2D2A ✓
CCDC186 ✓
CCDC22 ✓
CCDC88A ✓
CCDC88C ✓
CCL2 ✓
CCM2 ✓
CCND2 ✓
CDC42BPB ✓
CDK13 ✓
CDK19 ✓
CDK5 ✓
CDKL5 ✓
CELF2 ✓
CENPF ✓
CENPJ ✓
CEP290 ✓
CEP85L ✓
CERS1 ✓
CHD1 ✓
CHD2 ✓
CHD3 ✓
CHD4 ✓
CHD5 ✓
CHKA ✓
CHRNA2 ✓
CHRNA4 ✓
CHRNB2 ✓
CLCN2 ✓
CLCN3 ✓
CLCN4 ✓
CLDN5 ✓
CLN3 ✓
CLN5 ✓
CLN6 ✓
CLN8 ✓
CLPB ✓
CLTC ✓
CNKSR2 ✓
CNNM2 ✓
CNOT9 ✓
CNPY3 ✓
CNTN2 ✓
CNTNAP1 ✓
CNTNAP2 ✓
COG4 ✓
COG6 ✓
COG7 ✓
COG8 ✓
COL18A1 ✓
COL3A1 ✓
COL4A1 ✓
COL4A2 ✓
COL4A3BP ✓
COQ2 ✓
COQ4 ✓
COQ6 ✓
COQ8A ✓
COQ9 ✓
COX10 ✓
COX15 ✓
CP ✓
CPA6 ✓
CPLX1 ✓
CPSF3 ✓
CPT2 ✓
CRADD ✓
CREBBP ✓
CRH ✓
CSF1R ✓
CSNK1E ✓
CSNK2A1 ✓
CSNK2B ✓
CSTA ✓
CSTB ✓
CTNNA2 ✓
CTSA ✓
CTSD ✓
CTSF ✓
CTU2 ✓
CUL3 ✓
CUL4B ✓
CUX2 ✓
CWF19L1 ✓
CXorf56 ✓
CYFIP2 ✓
CYP27A1 ✓
D2HGDH ✓
DAG1 ✓
DBT ✓
DCHS1 ✓
DCX ✓
DDC ✓
DDX3X ✓
DEAF1 ✓
DEGS1 ✓
DENND5A ✓
DEPDC5 ✓
DHCR24 ✓
DHCR7 ✓
DHDDS ✓
DHFR ✓
DHPS ✓
DHX16 ✓
DHX30 ✓
DHX9 ✓
DIAPH1 ✓
DLD ✓
DLG4 ✓
DLL1 ✓
DMRTA2 ✓
DMXL2 ✓
DNAH14 ✓
DNAJC5 ✓
DNAJC6 ✓
DNM1 ✓
DNM1L ✓
DOCK7 ✓
DOHH ✓
DOLK ✓
DPAGT1 ✓
DPM1 ✓
DPM2 ✓
DPM3 ✓
DPYD ✓
DROSHA ✓
DYNC1H1 ✓
DYNC2H1 ✓
DYRK1A ✓
EARS2 ✓
ECHS1 ✓
ECM1 ✓
EED ✓
EEF1A2 ✓
EEF1B2 ✓
EFHC1 ✓
EFTUD2 ✓
EHMT1 ✓
EIF2AK2 ✓
EIF2B1 ✓
EIF2B2 ✓
EIF2B3 ✓
EIF2B4 ✓
EIF2B5 ✓
EIF2S3 ✓
EIF3F ✓
EIF4A2 ✓
ELOVL4 ✓
EMC1 ✓
EMC10 ✓
EML1 ✓
EMX2 ✓
EOMES ✓
EPG5 ✓
EPM2A ✓
ERMARD ✓
ESAM ✓
ETFDH ✓
ETHE1 ✓
EXOC7 ✓
EXOSC3 ✓
EXT2 ✓
FA2H ✓
FAR1 ✓
FARS2 ✓
FASN ✓
FASTKD2 ✓
FBXL4 ✓
FBXO11 ✓
FBXO28 ✓
FDFT1 ✓
FGD1 ✓
FGF12 ✓
FGF13 ✓
FGFR3 ✓
FH ✓
FIG4 ✓
FKRP ✓
FKTN ✓
FLNA ✓
FOLR1 ✓
FOXG1 ✓
FOXP1 ✓
FOXRED1 ✓
FRA10AC1 ✓
FRMD5 ✓
FRRS1L ✓
FUCA1 ✓
FUK ✓
FUT8 ✓
FZR1 ✓
GABBR2 ✓
GABRA1 ✓
GABRA2 ✓
GABRA3 ✓
GABRA4 ✓
GABRA5 ✓
GABRB1 ✓
GABRB2 ✓
GABRB3 ✓
GABRD ✓
GABRG2 ✓
GAD1 ✓
GALC ✓
GALNT2 ✓
GAMT ✓
GATAD2B ✓
GATM ✓
GBA ✓
GCDH ✓
GCH1 ✓
GCSH ✓
GFAP ✓
GFM1 ✓
GLB1 ✓
GLDC ✓
GLI2 ✓
GLI3 ✓
GLRA1 ✓
GLRB ✓
GLS ✓
GLUD1 ✓
GLUL ✓
GLYCTK ✓
GM2A ✓
GMPPA ✓
GMPPB ✓
GNAI1 ✓
GNAO1 ✓
GNB1 ✓
GNB5 ✓
GNE ✓
GNS ✓
GOSR2 ✓
GOT2 ✓
GPAA1 ✓
GPC3 ✓
GPHN ✓
GPSM2 ✓
GPT2 ✓
GRIA1 ✓
GRIA2 ✓
GRIA3 ✓
GRIA4 ✓
GRIK2 ✓
GRIN1 ✓
GRIN2A ✓
GRIN2B ✓
GRIN2D ✓
GRM7 ✓
GRN ✓
GSS ✓
GTPBP2 ✓
GTPBP3 ✓
H3F3A ✓
H3F3B ✓
HACE1 ✓
HAX1 ✓
HCCS ✓
HCFC1 ✓
HCN1 ✓
HCN2 ✓
HCN4 ✓
HDAC4 ✓
HDAC8 ✓
HECW2 ✓
HEPACAM ✓
HEXA ✓
HEXB ✓
HGSNAT ✓
HID1 ✓
HIVEP2 ✓
HLCS ✓
HMGCL ✓
HNRNPH2 ✓
HNRNPK ✓
HNRNPR ✓
HNRNPU ✓
HOXA1 ✓
HPD ✓
HPDL ✓
HPRT1 ✓
HRAS ✓
HSD17B10 ✓
HSD17B4 ✓
HSPD1 ✓
HTRA2 ✓
HTT ✓
IARS2 ✓
IBA57 ✓
IDH2 ✓
IDS ✓
IER3IP1 ✓
IFIH1 ✓
INTS8 ✓
IQSEC2 ✓
IRF2BPL ✓
ISPD ✓
ITGB4 ✓
ITPA ✓
JARID2 ✓
JMJD1C ✓
KANSL1 ✓
KARS ✓
KAT5 ✓
KAT6A ✓
KAT8 ✓
KATNB1 ✓
KCNA1 ✓
KCNA2 ✓
KCNA6 ✓
KCNAB2 ✓
KCNB1 ✓
KCNC1 ✓
KCNC2 ✓
KCND2 ✓
KCND3 ✓
KCNH1 ✓
KCNH2 ✓
KCNH5 ✓
KCNJ10 ✓
KCNJ11 ✓
KCNK4 ✓
KCNMA1 ✓
KCNN2 ✓
KCNQ2 ✓
KCNQ3 ✓
KCNQ5 ✓
KCNT1 ✓
KCNT2 ✓
KCNV2 ✓
KCTD3 ✓
KCTD7 ✓
KDM2B ✓
KDM4B ✓
KDM5A ✓
KDM5C ✓
KDM6A ✓
KIAA1109 ✓
KIF1A ✓
KIF1BP ✓
KIF2A ✓
KIF5A ✓
KIF5B ✓
KIF5C ✓
KLHL20 ✓
KMT2A ✓
KMT2B ✓
KMT2D ✓
KMT2E ✓
KMT5B ✓
KPNA7 ✓
KPTN ✓
KRAS ✓
KRIT1 ✓
L2HGDH ✓
LAMA2 ✓
LAMC3 ✓
LARGE1 ✓
LARS ✓
LBR ✓
LGI1 ✓
LIAS ✓
LIG3 ✓
LIPT2 ✓
LMBRD2 ✓
LMNB2 ✓
LMX1B ✓
LNPK ✓
LRBA ✓
LRPPRC ✓
LSS ✓
LYST ✓
MACF1 ✓
MADD ✓
MAF ✓
MANBA ✓
MAP1B ✓
MAP2K1 ✓
MAP2K2 ✓
MAPK10 ✓
MARCH6 ✓
MAST1 ✓
MAST3 ✓
MAST4 ✓
MBD5 ✓
MBOAT7 ✓
MCM3AP ✓
MCOLN1 ✓
MCPH1 ✓
MDH1 ✓
MDH2 ✓
ME2 ✓
MECP2 ✓
MED11 ✓
MED12 ✓
MED13L ✓
MED17 ✓
MED23 ✓
MED27 ✓
MEF2C ✓
MFF ✓
MFSD8 ✓
MGAT2 ✓
MINPP1 ✓
MLC1 ✓
MMACHC ✓
MMADHC ✓
MOCS1 ✓
MOCS2 ✓
MOGS ✓
MPDU1 ✓
MTHFR ✓
MTHFS ✓
MTOR ✓
MTR ✓
MYCBP2 ✓
MYT1L ✓
NAA10 ✓
NAA15 ✓
NACC1 ✓
NAGLU ✓
NALCN ✓
NAPB ✓
NARS ✓
NARS2 ✓
NAXE ✓
NBEA ✓
NCDN ✓
NDE1 ✓
NDP ✓
NDST1 ✓
NDUFA1 ✓
NDUFA10 ✓
NDUFA11 ✓
NDUFA2 ✓
NDUFA6 ✓
NDUFAF2 ✓
NDUFAF3 ✓
NDUFAF4 ✓
NDUFAF5 ✓
NDUFS1 ✓
NDUFS2 ✓
NDUFS3 ✓
NDUFS4 ✓
NDUFS6 ✓
NDUFS7 ✓
NDUFS8 ✓
NDUFV1 ✓
NECAP1 ✓
NEDD4L ✓
NEU1 ✓
NEUROD2 ✓
NEXMIF ✓
NF1 ✓
NGLY1 ✓
NHLRC1 ✓
NHLRC2 ✓
NIPBL ✓
NOTCH3 ✓
NOVA2 ✓
NPC1 ✓
NPC2 ✓
NPHP1 ✓
NPRL2 ✓
NPRL3 ✓
NR2F1 ✓
NR4A2 ✓
NRAS ✓
NRROS ✓
NRXN1 ✓
NSD1 ✓
NSDHL ✓
NSRP1 ✓
NTNG1 ✓
NTRK2 ✓
NUBPL ✓
NUP214 ✓
NUS1 ✓
OCLN ✓
OCRL ✓
OFD1 ✓
OGDHL ✓
OPHN1 ✓
OSGEP ✓
OTUD5 ✓
OTUD6B ✓
OTX2 ✓
OXR1 ✓
P4HTM ✓
PACS1 ✓
PACS2 ✓
PAFAH1B1 ✓
PAH ✓
PAK1 ✓
PAK2 ✓
PAK3 ✓
PANK2 ✓
PARP6 ✓
PARS2 ✓
PAX6 ✓
PC ✓
PCCA ✓
PCCB ✓
PCDH12 ✓
PCDH19 ✓
PCDHGC4 ✓
PCLO ✓
PCNT ✓
PCYT2 ✓
PDCD10 ✓
PDE2A ✓
PDHA1 ✓
PDHX ✓
PDSS2 ✓
PET100 ✓
PEX1 ✓
PEX10 ✓
PEX12 ✓
PEX13 ✓
PEX14 ✓
PEX19 ✓
PEX2 ✓
PEX26 ✓
PEX3 ✓
PEX5 ✓
PEX6 ✓
PEX7 ✓
PGAP2 ✓
PGAP3 ✓
PGK1 ✓
PHACTR1 ✓
PHF21A ✓
PHF6 ✓
PHGDH ✓
PI4K2A ✓
PIDD1 ✓
PIGA ✓
PIGB ✓
PIGC ✓
PIGF ✓
PIGG ✓
PIGH ✓
PIGK ✓
PIGL ✓
PIGM ✓
PIGN ✓
PIGO ✓
PIGP ✓
PIGQ ✓
PIGS ✓
PIGT ✓
PIGU ✓
PIGV ✓
PIGW ✓
PIK3C2B ✓
PIK3CA ✓
PIK3R2 ✓
PINK1 ✓
PIP5K1C ✓
PLA2G6 ✓
PLAA ✓
PLCB1 ✓
PLK1 ✓
PLP1 ✓
PLPBP ✓
PLXNA1 ✓
PLXNC1 ✓
PMM2 ✓
PMPCB ✓
PNKP ✓
PNPLA8 ✓
PNPO ✓
PNPT1 ✓
POGZ ✓
POLG ✓
POLG2 ✓
POLR1A ✓
POLR3B ✓
POMGNT1 ✓
POMGNT2 ✓
POMK ✓
POMT1 ✓
POMT2 ✓
POU3F3 ✓
PPFIBP1 ✓
PPIL1 ✓
PPP2CA ✓
PPP2R1A ✓
PPP2R5D ✓
PPP3CA ✓
PPT1 ✓
PQBP1 ✓
PRDM8 ✓
PRICKLE1 ✓
PRICKLE2 ✓
PRIMA1 ✓
PRMT7 ✓
PRNP ✓
PRODH ✓
PRPF8 ✓
PRRT2 ✓
PRUNE1 ✓
PSAP ✓
PSAT1 ✓
PSPH ✓
PTBP1 ✓
PTCH1 ✓
PTEN ✓
PTF1A ✓
PTPN11 ✓
PTPN23 ✓
PTS ✓
PUF60 ✓
PUM1 ✓
PURA ✓
PUS3 ✓
QARS ✓
QDPR ✓
RAB11A ✓
RAB11B ✓
RAB18 ✓
RAB39B ✓
RAB3GAP1 ✓
RAB3GAP2 ✓
RAB5C ✓
RABGAP1 ✓
RAC3 ✓
RAI1 ✓
RALA ✓
RALGAPA1 ✓
RAPGEF2 ✓
RARS2 ✓
RBFOX1 ✓
RBFOX3 ✓
RELN ✓
RERE ✓
RFT1 ✓
RHOBTB2 ✓
RMND1 ✓
RNASEH2A ✓
RNASEH2B ✓
RNASEH2C ✓
RNASET2 ✓
RNF113A ✓
RNF13 ✓
RNU4ATAC ✓
ROGDI ✓
RORA ✓
RORB ✓
RPGRIP1L ✓
RPH3A ✓
RPIA ✓
RPS6KA3 ✓
RRM2B ✓
RTN4IP1 ✓
RTTN ✓
RUSC2 ✓
RXYLT1 ✓
RYR3 ✓
SACS ✓
SAMD12 ✓
SAMHD1 ✓
SATB1 ✓
SATB2 ✓
SCAF4 ✓
SCAMP5 ✓
SCARB2 ✓
SCN10A ✓
SCN1A ✓
SCN1B ✓
SCN2A ✓
SCN3A ✓
SCN4A ✓
SCN5A ✓
SCN8A ✓
SCN9A ✓
SCO1 ✓
SCO2 ✓
SDHA ✓
SEMA6B ✓
SEPSECS ✓
SERAC1 ✓
SERPINI1 ✓
SETBP1 ✓
SETD1A ✓
SETD1B ✓
SETD5 ✓
SGSH ✓
SHANK3 ✓
SHH ✓
SHOC2 ✓
SIK1 ✓
SIX3 ✓
SLC12A5 ✓
SLC13A5 ✓
SLC16A2 ✓
SLC17A5 ✓
SLC19A3 ✓
SLC1A2 ✓
SLC1A3 ✓
SLC1A4 ✓
SLC22A5 ✓
SLC25A1 ✓
SLC25A12 ✓
SLC25A15 ✓
SLC25A19 ✓
SLC25A22 ✓
SLC2A1 ✓
SLC32A1 ✓
SLC35A1 ✓
SLC35A2 ✓
SLC35A3 ✓
SLC35C1 ✓
SLC38A3 ✓
SLC39A8 ✓
SLC45A1 ✓
SLC46A1 ✓
SLC4A10 ✓
SLC5A6 ✓
SLC6A1 ✓
SLC6A8 ✓
SLC7A6OS ✓
SLC9A6 ✓
SMARCA2 ✓
SMARCA4 ✓
SMARCB1 ✓
SMARCC2 ✓
SMARCE1 ✓
SMC1A ✓
SMC3 ✓
SMS ✓
SNAP25 ✓
SNAP29 ✓
SNIP1 ✓
SNX27 ✓
SON ✓
SOX11 ✓
SOX2 ✓
SPATA5 ✓
SPATA5L1 ✓
SPR ✓
SPRED1 ✓
SPTAN1 ✓
SPTBN1 ✓
SPTBN4 ✓
SRCAP ✓
SRGAP2 ✓
ST3GAL3 ✓
ST3GAL5 ✓
STAG1 ✓
STAMBP ✓
STARD7 ✓
STIL ✓
STRADA ✓
STX1A ✓
STX1B ✓
STXBP1 ✓
SUCLA2 ✓
SUCLG1 ✓
SUMF1 ✓
SUOX ✓
SURF1 ✓
SYN1 ✓
SYNE1 ✓
SYNGAP1 ✓
SYNJ1 ✓
SYP ✓
SZT2 ✓
TACO1 ✓
TAF1C ✓
TAF8 ✓
TANC2 ✓
TANGO2 ✓
TAOK1 ✓
TARS2 ✓
TBC1D20 ✓
TBC1D24 ✓
TBC1D2B ✓
TBC1D7 ✓
TBCD ✓
TBCK ✓
TBL1XR1 ✓
TBX1 ✓
TBX19 ✓
TCEAL1 ✓
TCF4 ✓
TDP2 ✓
TELO2 ✓
TET3 ✓
TFE3 ✓
TGIF1 ✓
THG1L ✓
THOC2 ✓
TIAM1 ✓
TIMM50 ✓
TK2 ✓
TLK2 ✓
TMEM106B ✓
TMEM222 ✓
TMEM63B ✓
TMEM67 ✓
TMEM70 ✓
TMTC3 ✓
TMX2 ✓
TNK2 ✓
TNPO2 ✓
TNRC6A ✓
TPK1 ✓
TPP1 ✓
TRA2B ✓
TRAF7 ✓
TRAK1 ✓
TRAPPC10 ✓
TRAPPC11 ✓
TRAPPC12 ✓
TRAPPC4 ✓
TRAPPC6B ✓
TREM2 ✓
TREX1 ✓
TRIM8 ✓
TRIO ✓
TRIP12 ✓
TRIT1 ✓
TRMT1 ✓
TRMT10A ✓
TRPM3 ✓
TRPM6 ✓
TRRAP ✓
TSC1 ✓
TSC2 ✓
TSEN15 ✓
TSEN2 ✓
TSEN34 ✓
TSEN54 ✓
TSFM ✓
TSPYL1 ✓
TTC5 ✓
TUBA1A ✓
TUBA8 ✓
TUBB ✓
TUBB2A ✓
TUBB2B ✓
TUBB3 ✓
TUBB4A ✓
TUBG1 ✓
TUBGCP2 ✓
TUBGCP6 ✓
TWNK ✓
U2AF2 ✓
UBA5 ✓
UBAP2L ✓
UBE2A ✓
UBE3A ✓
UBR7 ✓
UBTF ✓
UFM1 ✓
UFSP2 ✓
UGDH ✓
UGGT1 ✓
UGP2 ✓
UMPS ✓
UNC79 ✓
UNC80 ✓
USP18 ✓
VAMP2 ✓
VARS ✓
VARS2 ✓
VLDLR ✓
VPS11 ✓
VPS13A ✓
VPS13B ✓
VPS13D ✓
VPS4A ✓
WAC ✓
WARS2 ✓
WASF1 ✓
WASHC4 ✓
WDFY3 ✓
WDR26 ✓
WDR37 ✓
WDR45 ✓
WDR45B ✓
WDR5 ✓
WDR62 ✓
WDR73 ✓
WNK3 ✓
WWOX ✓
XPR1 ✓
YEATS2 ✓
YIF1B ✓
YIPF5 ✓
YWHAE ✓
YWHAG ✓
ZBTB18 ✓
ZDHHC9 ✓
ZEB2 ✓
ZIC2 ✓
ZMIZ1 ✓
ZMYND11 ✓
ZMYND8 ✓
ZNF142 ✓
ZNF148 ✓
ZNF335 ✓
ZNF526 ✓
ZNHIT3 ✓
ZSWIM6 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Brown Vialetto-Van Laere syndrome gene panel

MHL Testcode : GG58
Methodology : NGS
Disease Segment : Neurology
TAT : 28
Key genes :

+ Show Genes

×

SLC52A2 & SLC52A3 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Calpainopathy and LGMD2A , deletion and duplication analysis

MHL Testcode : GG59
Methodology : MLPA
Disease Segment : Neurology
TAT : 21
Key genes :

+ Show Genes

×

CAPN3 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Canavan disease , gene analysis

MHL Testcode : GG60
Methodology : NGS
Disease Segment : Neurology
TAT : 28
Key genes :

+ Show Genes

×

ASPA ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen CAPN3 gene sequencing

MHL Testcode : GG61
Methodology : NGS
Disease Segment : Neurology
TAT : 28
Key genes :

+ Show Genes

×

CAPN3 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Cerebral Cavernous Malformation gene Panel

MHL Testcode : GG62
Methodology : NGS
Disease Segment : Neurology
TAT : 28
Key genes :

+ Show Genes

×

CCM2 ✓
KRIT1 ✓
PDCD10 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Charcot-Marie-Tooth 1A and HNPP , deletion and duplication analysis

MHL Testcode : GG63
Methodology : MLPA
Disease Segment : Neurology
TAT : 21
Key genes :

+ Show Genes

×

PMP22 ✓
COX10 ✓
TEKT3 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Charcot-Marie-Tooth and sensory neuropathies gene panel

MHL Testcode : GG64
Methodology : NGS
Disease Segment : Neurology
TAT : 28
Key genes :

+ Show Genes

×

AARS ✓
AIFM1 ✓
ATL1 ✓
ATL3 ✓
CCT5 ✓
COX6A1 ✓
CTDP1 ✓
DHTKD1 ✓
DNAJB2 ✓
DNM2 ✓
DNMT1 ✓
DST ✓
DYNC1H1 ✓
EGR2 ✓
FAM134B ✓
FGD4 ✓
FIG4 ✓
GAN ✓
GARS ✓
GDAP1 ✓
GJB1 ✓
GNB4 ✓
HARS ✓
HINT1 ✓
HK1 ✓
HOXD10 ✓
HSPB1 ✓
HSPB8 ✓
IGHMBP2 ✓
INF2 ✓
JPH1 ✓
KARS ✓
KIF1A ✓
KIF1B ✓
KIF5A ✓
LITAF ✓
LMNA ✓
LRSAM1 ✓
MARS ✓
MED25 ✓
MFN2 ✓
MME ✓
MORC2 ✓
MPZ ✓
MTMR2 ✓
NAGLU ✓
NDRG1 ✓
NEFH ✓
NEFL ✓
NGF ✓
NTRK1 ✓
PDK3 ✓
PLEKHG5 ✓
PMP22 ✓
PRDM12 ✓
PRPS1 ✓
PRX ✓
RAB7A ✓
REEP1 ✓
SBF1 ✓
SBF2 ✓
SCN11A ✓
SCN9A ✓
SH3TC2 ✓
SLC12A6 ✓
SLC25A46 ✓
SOX10 ✓
SPG11 ✓
SPTLC1 ✓
SPTLC2 ✓
SURF1 ✓
TFG ✓
TRIM2 ✓
TRPV4 ✓
TTR ✓
VCP ✓
WNK1 ✓
YARS ✓
✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Charcot-Marie-Tooth type 4 , deletion and duplication analysis

MHL Testcode : GG65
Methodology : MLPA
Disease Segment : Neurology
TAT : 21
Key genes :

+ Show Genes

×

EGR2 ✓
GDAP1 ✓
NEFL ✓
PRX ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Charcot-Marie-Tooth type 4C , deletion and duplication analysis

MHL Testcode : GG66
Methodology : MLPA
Disease Segment : Neurology
TAT : 21
Key genes :

+ Show Genes

×

SH3TC2 ✓
✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen CLP1 gene sequencing

MHL Testcode : GG67
Methodology : NGS
Disease Segment : Neurology
TAT : 28
Key genes :

+ Show Genes

×

CLP1 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Coenzyme q10 Deficiency gene panel

MHL Testcode : GG68
Methodology : NGS
Disease Segment : Neurology
TAT : 28
Key genes :

+ Show Genes

×

APTX ✓
COQ2 ✓
COQ4 ✓
COQ6 ✓
COQ8A ✓
COQ8B ✓
COQ9 ✓
ETFA ✓
ETFB ✓
ETFDH ✓
PDSS1 ✓
PDSS2 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Collagen Type VI-Related Disorders gene panel

MHL Testcode : GG69
Methodology : NGS
Disease Segment : Neurology
TAT : 28
Key genes :

+ Show Genes

×

COL12A1 ✓
COL4A1 ✓
COL4A2 ✓
COL6A1 ✓
COL6A2 ✓
COL6A3 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Congenital Muscular Dystrophy , deletion and duplication analysis

MHL Testcode : GG70
Methodology : MLPA
Disease Segment : Neurology
TAT : 21
Key genes :

+ Show Genes

×

LAMA2 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Comprehensive neurology gene panel

MHL Testcode : GG71
Methodology : NGS
Disease Segment : Neurology
TAT : 28
Key genes :

+ Show Genes

×

1476 Genes ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Congenital Myasthenic Syndromes gene Panel

MHL Testcode : GG72
Methodology : NGS
Disease Segment : Neurology
TAT : 28
Key genes :

+ Show Genes

×

CSTB ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Creatine Metabolism Deficiency gene Panel

MHL Testcode : GG73
Methodology : NGS
Disease Segment : Neurology
TAT : 28
Key genes :

+ Show Genes

×

GATM ✓
GAMT ✓
SLC6A8 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen CSTB gene sequencing

MHL Testcode : GG74
Methodology : NGS
Disease Segment : Neurology
TAT : 28
Key genes :

+ Show Genes

×

CSTB ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Cystic megalencephaly , gene analysis

MHL Testcode : GG75
Methodology : NGS
Disease Segment : Neurology
TAT : 28
Key genes :

+ Show Genes

×

MLC1 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Dementia gene Panel

MHL Testcode : GG76
Methodology : NGS
Disease Segment : Neurology
TAT : 28
Key genes :

+ Show Genes

×

ABCA7 ✓
APOE ✓
APP ✓
CHMP2B ✓
CSF1R ✓
FUS ✓
GRN ✓
MAPT ✓
PRNP ✓
PSEN1 ✓
PSEN2 ✓
RNF216 ✓
SIGMAR1 ✓
SNCA ✓
SORL1 ✓
TARDBP ✓
TREM2 ✓
TUBA4A ✓
UBE3A ✓
UBQLN2 ✓
VCP ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Dravet syndrome , deletion and duplication analysis

MHL Testcode : GG77
Methodology : MLPA
Disease Segment : Neurology
TAT : 21
Key genes :

+ Show Genes

×

SCN1A ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Dravet syndrome , gene analysis

MHL Testcode : GG78
Methodology : NGS
Disease Segment : Neurology
TAT : 28
Key genes :

+ Show Genes

×

SCN1A ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Duchenne Muscular Dystrophy , deletion and duplication analysis

MHL Testcode : GG79
Methodology : MLPA
Disease Segment : Neurology
TAT : 21
Key genes :

+ Show Genes

×

DMD ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Duchenne Muscular Dystrophy , gene sequencing

MHL Testcode : GG80
Methodology : NGS
Disease Segment : Neurology
TAT : 28
Key genes :

+ Show Genes

×

DMD ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen DYSF gene sequencing

MHL Testcode : GG81
Methodology : NGS
Disease Segment : Neurology
TAT : 28
Key genes :

+ Show Genes

×

DYSF ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Dysferlinopathy and LGMD2B , deletion and duplication analysis

MHL Testcode : GG82
Methodology : MLPA
Disease Segment : Neurology
TAT : 21
Key genes :

+ Show Genes

×

DYSF ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Dystonia gene panel

MHL Testcode : GG83
Methodology : NGS
Disease Segment : Neurology
TAT : 28
Key genes :

+ Show Genes

×

ACTB ✓
ADAR ✓
ADCY5 ✓
AFG3L2 ✓
ALDH5A1 ✓
ANO3 ✓
ARSA ✓
ARX ✓
ATP1A3 ✓
ATP6AP2 ✓
ATP7B ✓
AUH ✓
BCAP31 ✓
BCS1L ✓
C10orf2 ✓
C19orf12 ✓
CACNA1A ✓
CACNA1B ✓
CACNA1G ✓
CCDC88C ✓
CDKL5 ✓
CIZ1 ✓
COASY ✓
COL6A3 ✓
COX10 ✓
COX15 ✓
COX20 ✓
CP ✓
DDC ✓
DLAT ✓
DLD ✓
DNAJC13 ✓
DNAJC6 ✓
DRD2 ✓
EEF2 ✓
ELOVL4 ✓
ELOVL5 ✓
FA2H ✓
FBXO7 ✓
FGF14 ✓
FOLR1 ✓
FOXG1 ✓
FTL ✓
FUS ✓
GCDH ✓
GCH1 ✓
GNAL ✓
HEXA ✓
HPCA ✓
HTRA2 ✓
IFIH1 ✓
ITPR1 ✓
KCNC3 ✓
KCND3 ✓
KCNMA1 ✓
KCTD17 ✓
KMT2B ✓
LRPPRC ✓
LRRK2 ✓
MAPT ✓
MECP2 ✓
MR1 ✓
MTTP ✓
NDUFA10 ✓
NDUFA12 ✓
NDUFA2 ✓
NDUFA9 ✓
NDUFAF2 ✓
NDUFAF5 ✓
NDUFAF6 ✓
NDUFS1 ✓
NDUFS3 ✓
NDUFS4 ✓
NDUFS7 ✓
NDUFS8 ✓
NKX2-1 ✓
NPC1 ✓
NPC2 ✓
NUP62 ✓
PAH ✓
PANK2 ✓
PARK2 ✓
PARK7 ✓
PCBD1 ✓
PDHA1 ✓
PDHB ✓
PDHX ✓
PDYN ✓
PINK1 ✓
PLA2G6 ✓
PLP1 ✓
PNKD ✓
POLG ✓
PPP2R2B ✓
PRKAG2 ✓
PRKCG ✓
PRKRA ✓
PRRT2 ✓
PTS ✓
QDPR ✓
RNASEH2A ✓
RNASEH2B ✓
RNASEH2C ✓
SAMHD1 ✓
SCO2 ✓
SERAC1 ✓
SGCE ✓
SLC16A2 ✓
SLC19A3 ✓
SLC2A1 ✓
SLC30A10 ✓
SLC6A19 ✓
SLC6A3 ✓
SMPD1 ✓
SNCA ✓
SPG11 ✓
SPG7 ✓
SPR ✓
SPTBN2 ✓
SUCLA2 ✓
SUCLG1 ✓
SURF1 ✓
SYNJ1 ✓
TACO1 ✓
TAF1 ✓
TGM6 ✓
TH ✓
THAP1 ✓
TIMM8A ✓
TMEM240 ✓
TOR1A ✓
TREX1 ✓
TRPC3 ✓
TTBK2 ✓
TUBB4A ✓
UCHL1 ✓
VPS13A ✓
VPS35 ✓
WDR45 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Dystonia 28 , gene sequencing

MHL Testcode : GG84
Methodology : NGS
Disease Segment : Neurology
TAT : 28
Key genes :

+ Show Genes

×

KMT2B ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Early infantile epileptic encephalopathy-4 , deletion and duplication analysis

MHL Testcode : GG85
Methodology : MLPA
Disease Segment : Neurology
TAT : 21
Key genes :

+ Show Genes

×

STXBP1 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Early-onset juvenile parkinsonism gene panel

MHL Testcode : GG86
Methodology : NGS
Disease Segment : Neurology
TAT : 28
Key genes :

+ Show Genes

×

ATP13A2 ✓
DNAJC6 ✓
FBXO7 ✓
LRRK2 ✓
PARK2 ✓
PARK7 ✓
PINK1 ✓
PLA2G6 ✓
RAB39B ✓
SLC6A3 ✓
SNCA ✓
SYNJ1 ✓
VAC14 ✓
VPS13C ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Emery-Dreifuss Muscular Dystrophy gene Panel

MHL Testcode : GG87
Methodology : NGS
Disease Segment : Neurology
TAT : 28
Key genes :

+ Show Genes

×

EMD ✓
LMNA ✓
SYNE1 ✓
SYNE2 ✓
FHL1 ✓
TMEM43 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Epileptic encephalopathy gene panel

MHL Testcode : GG88
Methodology : NGS
Disease Segment : Neurology
TAT : 28
Key genes :

+ Show Genes

×

AARS ✓
ABAT ✓
ABCC8 ✓
ALDH7A1 ✓
ALG13 ✓
AMT ✓
AP3B2 ✓
ARHGEF9 ✓
ARV1 ✓
ARX ✓
ATP13A2 ✓
ATP7A ✓
CACNA1A ✓
CACNA1H ✓
CACNB4 ✓
CAD ✓
CDKL5 ✓
CHD2 ✓
CHRNA2 ✓
CHRNA4 ✓
CHRNB2 ✓
CLCN2 ✓
CLN3 ✓
CLN5 ✓
CLN6 ✓
CLN8 ✓
CLTC ✓
CNPY3 ✓
CTSD ✓
CTSF ✓
D2HGDH ✓
DENND5A ✓
DHDDS ✓
DNAJC5 ✓
DNM1 ✓
DOCK7 ✓
EEF1A2 ✓
FGF12 ✓
FOXG1 ✓
FRRS1L ✓
GABBR2 ✓
GABRA1 ✓
GABRA2 ✓
GABRA3 ✓
GABRB2 ✓
GABRB3 ✓
GABRD ✓
GABRG2 ✓
GAMT ✓
GLDC ✓
GNAO1 ✓
GRIN2B ✓
GRIN2D ✓
GRN ✓
GUF1 ✓
HCN1 ✓
HNRNPU ✓
HSD17B4 ✓
IDH2 ✓
ITPA ✓
KCNA2 ✓
KCNB1 ✓
KCNJ11 ✓
KCNQ2 ✓
KCNQ3 ✓
KCNT1 ✓
KCTD7 ✓
MBD5 ✓
MDH2 ✓
MECP2 ✓
MFSD8 ✓
MICAL1 ✓
NECAP1 ✓
NTRK2 ✓
NUS1 ✓
PC ✓
PCDH19 ✓
PEX1 ✓
PEX10 ✓
PEX12 ✓
PEX26 ✓
PEX6 ✓
PIGA ✓
PLCB1 ✓
PNKP ✓
PNPO ✓
PPT1 ✓
PTPN23 ✓
RHOBTB2 ✓
SCN1A ✓
SCN1B ✓
SCN2A ✓
SCN3A ✓
SCN8A ✓
SCN9A ✓
SIK1 ✓
SLC12A5 ✓
SLC13A5 ✓
SLC1A2 ✓
SLC25A22 ✓
SLC2A1 ✓
SLC35A2 ✓
SNAP25 ✓
SPTAN1 ✓
ST3GAL3 ✓
STXBP1 ✓
SUOX ✓
SYNJ1 ✓
SZT2 ✓
TBC1D24 ✓
TCF4 ✓
TPP1 ✓
TSC1 ✓
TSC2 ✓
UBA5 ✓
UBE3A ✓
WDR45 ✓
WWOX ✓
ZEB2 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Episodic ataxia gene panel

MHL Testcode : GG89
Methodology : NGS
Disease Segment : Neurology
TAT : 28
Key genes :

+ Show Genes

×

CACNA1A ✓
CACNB4 ✓
KCNA1 ✓
SLC1A3 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Familial female mental retardation and epilepsy gene panel

MHL Testcode : GG90
Methodology : NGS
Disease Segment : Neurology
TAT : 28
Key genes :

+ Show Genes

×

ALDH7A1 ✓
ARX ✓
ATRX ✓
CASK ✓
CDKL5 ✓
CUL4B ✓
FOLR1 ✓
GRIA3 ✓
HSD17B10 ✓
IQSEC2 ✓
KCNQ2 ✓
KCNQ3 ✓
KDM5C ✓
MECP2 ✓
MED12 ✓
MEF2C ✓
OPHN1 ✓
PCDH19 ✓
PGK1 ✓
PHF6 ✓
PNPO ✓
POLG ✓
SCN1A ✓
SCN1B ✓
SCN2A ✓
SCN8A ✓
SLC2A1 ✓
SLC9A6 ✓
SPTAN1 ✓
STXBP1 ✓
UBE2A ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Familial hemiplegic migraine gene panel

MHL Testcode : GG91
Methodology : NGS
Disease Segment : Neurology
TAT : 28
Key genes :

+ Show Genes

×

ATP1A2 ✓
CACNA1A ✓
PRRT2 ✓
SCN1A ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Familial temporal lobe epilepsy-1 , gene sequencing

MHL Testcode : GG92
Methodology : NGS
Disease Segment : Neurology
TAT : 28
Key genes :

+ Show Genes

×

LGI1 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Friedreich ataxia , - Repeat expansion analysis

MHL Testcode : GG93
Methodology : Fragment Analysis
Disease Segment : Neurology
TAT : 28
Key genes :

+ Show Genes

×

FXN ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Fukuyama Congenital Muscular Dystrophy , gene sequencing ,

MHL Testcode : GG94
Methodology : NGS
Disease Segment : Neurology
TAT : 28
Key genes :

+ Show Genes

×

FKTN ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen GAN and DCAF8 gene sequencing

MHL Testcode : GG95
Methodology : NGS
Disease Segment : Neurology
TAT : 28
Key genes :

+ Show Genes

×

GAN and DCAF8 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen GBE1 gene sequencing

MHL Testcode : GG96
Methodology : NGS
Disease Segment : Neurology
TAT : 28
Key genes :

+ Show Genes

×

GBE1 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen GCH1 gene sequencing

MHL Testcode : GG97
Methodology : NGS
Disease Segment : Neurology
TAT : 28
Key genes :

+ Show Genes

×

GCH1 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Giant axonal neuropathy-1 , gene analysis

MHL Testcode : GG98
Methodology : NGS
Disease Segment : Neurology
TAT : 28
Key genes :

+ Show Genes

×

GAN ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Gordon Holmes syndrome , gene sequencing

MHL Testcode : GG99
Methodology : NGS
Disease Segment : Neurology
TAT : 28
Key genes :

+ Show Genes

×

RNF216 and OTUD4 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Hereditary essential tremor , gene sequencing

MHL Testcode : GG100
Methodology : NGS
Disease Segment : Neurology
TAT : 28
Key genes :

+ Show Genes

×

FUS and TENM4 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Hereditary spastic paraplegia gene panel

MHL Testcode : GG101
Methodology : NGS
Disease Segment : Neurology
TAT : 28
Key genes :

+ Show Genes

×

ABCD1 ✓
ALDH18A1 ✓
ALS2 ✓
AMPD2 ✓
AP4B1 ✓
AP4E1 ✓
AP4M1 ✓
AP4S1 ✓
AP5Z1 ✓
ARL6IP1 ✓
ATL1 ✓
ATP13A2 ✓
B4GALNT1 ✓
BICD2 ✓
BSCL2 ✓
C12orf65 ✓
C19orf12 ✓
CAPN1 ✓
CCT5 ✓
CPT1C ✓
CYP2U1 ✓
CYP7B1 ✓
DDHD1 ✓
DDHD2 ✓
ENTPD1 ✓
ERLIN1 ✓
ERLIN2 ✓
EXOSC3 ✓
FA2H ✓
FARS2 ✓
FLRT1 ✓
GAD1 ✓
GBA ✓
GBA2 ✓
GJC2 ✓
HSPD1 ✓
IBA57 ✓
KIAA0196 ✓
KIDINS220 ✓
KIF1A ✓
KIF1C ✓
KIF5A ✓
KLC2 ✓
L1CAM ✓
LYST ✓
MAG ✓
NIPA1 ✓
NT5C2 ✓
PLP1 ✓
PNPLA6 ✓
REEP1 ✓
REEP2 ✓
RTN2 ✓
SACS ✓
SLC16A2 ✓
SLC1A4 ✓
SLC2A1 ✓
SLC33A1 ✓
SPAST ✓
SPG11 ✓
SPG20 ✓
SPG21 ✓
SPG7 ✓
TECPR2 ✓
TFG ✓
USP8 ✓
VAMP1 ✓
VPS37A ✓
ZFYVE26 ✓
ZFYVE27 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen HINT1 gene sequencing

MHL Testcode : GG102
Methodology : NGS
Disease Segment : Neurology
TAT : 28
Key genes :

+ Show Genes

×

HINT1 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Holoprosencephaly gene Panel

MHL Testcode : GG103
Methodology : NGS
Disease Segment : Neurology
TAT : 28
Key genes :

+ Show Genes

×

CDON ✓
CRIPTO ✓
DISP1 ✓
DLL1 ✓
FGF8 ✓
FOXH1 ✓
GAS1 ✓
GLI2 ✓
NODAL ✓
PTCH1 ✓
SHH ✓
SIX3 ✓
TGIF1 ✓
ZIC2 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Huntington's disease , - Repeat expansion analysis

MHL Testcode : GG104
Methodology : Fragment Analysis
Disease Segment : Neurology
TAT : 28
Key genes :

+ Show Genes

×

HTT ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Hyperekplexia gene panel

MHL Testcode : GG105
Methodology : NGS
Disease Segment : Neurology
TAT : 28
Key genes :

+ Show Genes

×

ARHGEF9 ✓
GLRA1 ✓
GLRB ✓
SLC6A5 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Hypomyelination syndrome gene panel

MHL Testcode : GG106
Methodology : NGS
Disease Segment : Neurology
TAT : 28
Key genes :

+ Show Genes

×

AIMP1 ✓
BCAP31 ✓
C11ORF73 ✓
DARS ✓
EGR2 ✓
EIF2B1 ✓
EIF2B2 ✓
EIF2B3 ✓
EIF2B4 ✓
EIF2B5 ✓
ERCC4 ✓
ERCC5 ✓
ERCC6 ✓
ERCC8 ✓
EXOSC8 ✓
FAM126A ✓
GJC2 ✓
HSPD1 ✓
MLC1 ✓
MPZ ✓
PLP1 ✓
POLR1C ✓
POLR3A ✓
POLR3B ✓
PYCR2 ✓
RARS ✓
SLC25A12 ✓
SLC33A1 ✓
SPTAN1 ✓
STXBP1 ✓
TBCD ✓
TUBB4A ✓
VPS11 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Idiopathic Generalized and Focal Epilepsy gene Panel

MHL Testcode : GG107
Methodology : NGS
Disease Segment : Neurology
TAT : 28
Key genes :

+ Show Genes

×

ALDH7A1 ✓
AMACR ✓
CACNA1H ✓
CACNB4 ✓
CASR ✓
CHRNA2 ✓
CHRNA4 ✓
CHRNB2 ✓
CLCN2 ✓
DEPDC5 ✓
EFHC1 ✓
GABRA1 ✓
GABRB3 ✓
GABRG2 ✓
GRIN2A ✓
KCNA1 ✓
KCNC1 ✓
KCNQ2 ✓
KCNQ3 ✓
KCNT1 ✓
LGI1 ✓
MTOR ✓
POLG ✓
PRRT2 ✓
RELN ✓
SCN1A ✓
SCN1B ✓
SCN2A ✓
SCN8A ✓
SCN9A ✓
SLC2A1 ✓
SLC6A1 ✓
STX1B ✓
TBC1D24 ✓
✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen IGHMBP2 gene sequencing

MHL Testcode : GG108
Methodology : NGS
Disease Segment : Neurology
TAT : 28
Key genes :

+ Show Genes

×

IGHMBP2 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Joubert syndrome gene panel

MHL Testcode : GG109
Methodology : NGS
Disease Segment : Neurology
TAT : 28
Key genes :

+ Show Genes

×

AHI1 ✓
ARL13B ✓
B9D1 ✓
C2CD3 ✓
C5orf42 ✓
CC2D2A ✓
CEP104 ✓
CEP290 ✓
CEP41 ✓
CSPP1 ✓
DDX59 ✓
INPP5E ✓
KIAA0556 ✓
KIAA0586 ✓
KIAA0753 ✓
KIF7 ✓
LAMA1 ✓
MKS1 ✓
NPHP1 ✓
OFD1 ✓
PDE6D ✓
RPGRIP1L ✓
TCTN1 ✓
TCTN2 ✓
TCTN3 ✓
TMEM138 ✓
TMEM216 ✓
TMEM231 ✓
TMEM237 ✓
TMEM67 ✓
TTC21B ✓
ZNF423 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen KCNT1 gene sequencing

MHL Testcode : GG110
Methodology : NGS
Disease Segment : Neurology
TAT : 28
Key genes :

+ Show Genes

×

KCNT1 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Krabbe disease , deletion and duplication analysis

MHL Testcode : GG111
Methodology : MLPA
Disease Segment : Neurology
TAT : 28
Key genes :

+ Show Genes

×

GALC ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Krabbe disease , gene analysis

MHL Testcode : GG112
Methodology : NGS
Disease Segment : Neurology
TAT : 21
Key genes :

+ Show Genes

×

GALC ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Leukodystrophy and Leukoencephalopathy gene Panel

MHL Testcode : GG113
Methodology : NGS
Disease Segment : Neurology
TAT : 28
Key genes :

+ Show Genes

×

AARS2 ✓
ABCD1 ✓
ACOX1 ✓
ACP5 ✓
ADAR ✓
ADGRG1 ✓
ADSL ✓
AGA ✓
AIMP1 ✓
AIMP2 ✓
ALDH3A2 ✓
ALDH5A1 ✓
ARSA ✓
ASPA ✓
ATP7A ✓
ATP7B ✓
BCAP31 ✓
BOLA3 ✓
BPTF ✓
CBS ✓
CLCN2 ✓
CLDN11 ✓
CLPP ✓
CNP ✓
CNTNAP1 ✓
COA8 ✓
COL4A1 ✓
COL4A2 ✓
COLGALT1 ✓
COQ2 ✓
COQ9 ✓
COX10 ✓
COX15 ✓
CPS1 ✓
CSF1R ✓
CTC1 ✓
CTSA ✓
CYP27A1 ✓
CYP2U1 ✓
CYP7B1 ✓
D2HGDH ✓
DAG1 ✓
DARS1 ✓
DARS2 ✓
DCAF17 ✓
DDHD2 ✓
DEGS1 ✓
DGUOK ✓
DNM1L ✓
EARS2 ✓
EIF2B1 ✓
EIF2B2 ✓
EIF2B3 ✓
EIF2B4 ✓
EIF2B5 ✓
EPRS1 ✓
ERCC6 ✓
ERCC8 ✓
ETFA ✓
ETFB ✓
ETFDH ✓
FA2H ✓
FARS2 ✓
FBXL4 ✓
FDFT1 ✓
FDX2 ✓
FH ✓
FOLR1 ✓
FOXRED1 ✓
FUCA1 ✓
GALC ✓
GALT ✓
GAN ✓
GBE1 ✓
GCDH ✓
GFAP ✓
GFM1 ✓
GJA1 ✓
GJB1 ✓
GJC2 ✓
GLA ✓
GLB1 ✓
HEPACAM ✓
HEXA ✓
HIKESHI ✓
HMGCL ✓
HSD17B4 ✓
HSPD1 ✓
HTRA1 ✓
HYCC1 ✓
IBA57 ✓
IDH2 ✓
IDS ✓
IFIH1 ✓
ISCA2 ✓
JAM3 ✓
KARS1 ✓
L2HGDH ✓
LAMA2 ✓
LMNB1 ✓
LRPPRC ✓
LYRM7 ✓
MARS2 ✓
MCOLN1 ✓
MLC1 ✓
MOCS1 ✓
MRPS22 ✓
MTFMT ✓
MTHFR ✓
MTHFS ✓
MYRF ✓
NAXD ✓
NAXE ✓
NDUFA1 ✓
NDUFA10 ✓
NDUFA12 ✓
NDUFA2 ✓
NDUFA9 ✓
NDUFAF2 ✓
NDUFAF4 ✓
NDUFAF5 ✓
NDUFAF6 ✓
NDUFB8 ✓
NDUFS1 ✓
NDUFS2 ✓
NDUFS3 ✓
NDUFS4 ✓
NDUFS7 ✓
NDUFS8 ✓
NDUFV1 ✓
NFU1 ✓
NKX6-2 ✓
NOTCH3 ✓
NPC1 ✓
NPC2 ✓
NUBPL ✓
OCLN ✓
OCRL ✓
OSGEP ✓
OTC ✓
PAH ✓
PC ✓
PDHA1 ✓
PEX1 ✓
PEX10 ✓
PEX11B ✓
PEX12 ✓
PEX13 ✓
PEX14 ✓
PEX16 ✓
PEX19 ✓
PEX2 ✓
PEX26 ✓
PEX3 ✓
PEX5 ✓
PEX6 ✓
PLAA ✓
PLEKHG2 ✓
PLP1 ✓
POLG ✓
POLR1A ✓
POLR1C ✓
POLR3A ✓
POLR3B ✓
POLR3K ✓
PPT1 ✓
PSAP ✓
PYCR2 ✓
RARS1 ✓
REEP1 ✓
RNASEH2A ✓
RNASEH2B ✓
RNASEH2C ✓
RNASET2 ✓
RNF216 ✓
RNF220 ✓
RRM2B ✓
SAMHD1 ✓
SCP2 ✓
SDHAF1 ✓
SDHB ✓
SLC16A2 ✓
SLC17A5 ✓
SLC19A3 ✓
SLC25A1 ✓
SLC25A12 ✓
SLC25A4 ✓
SLC6A9 ✓
SNORD118 ✓
SOX10 ✓
SPART ✓
SPG11 ✓
SPG7 ✓
STN1 ✓
SUCLA2 ✓
SUMF1 ✓
SURF1 ✓
TMEM106B ✓
TMEM63A ✓
TREM2 ✓
TREX1 ✓
TUBB4A ✓
TUFM ✓
TWNK ✓
TYMP ✓
TYROBP ✓
UFM1 ✓
UPB1 ✓
VPS11 ✓
WARS2 ✓
YY1 ✓
ZFYVE26 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen LGMD and Congenital Muscular Dystrophy gene Panel

MHL Testcode : GG114
Methodology : NGS
Disease Segment : Neurology
TAT : 28
Key genes :

+ Show Genes

×

ANO5 ✓
B3GALNT2 ✓
CAPN3 ✓
CAV3 ✓
COL4A1 ✓
COL4A2 ✓
CRPPA ✓
CRYAB ✓
DES ✓
DMD ✓
DNAJB6 ✓
DYSF ✓
FKRP ✓
FKTN ✓
GMPPB ✓
ITGA7 ✓
LAMA2 ✓
LARGE1 ✓
LIMS2 ✓
LMNA ✓
MEGF10 ✓
MYH7 ✓
MYOT ✓
PNPLA2 ✓
POGLUT1 ✓
POMGNT2 ✓
POMT1 ✓
SELENON ✓
SGCA ✓
SGCB ✓
SGCD ✓
SGCG ✓
SMCHD1 ✓
SPEG ✓
SYNE1 ✓
TCAP ✓
TNPO3 ✓
TOR1AIP1 ✓
TRAPPC11 ✓
TRIM32 ✓
TTN ✓
VMA21 ✓
✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Lissencephaly gene panel

MHL Testcode : GG116
Methodology : NGS
Disease Segment : Neurology
TAT : 28
Key genes :

+ Show Genes

×

ACTB ✓
ACTG1 ✓
ADGRG1 ✓
ARX ✓
ATP6V0A2 ✓
B3GALNT2 ✓
B4GAT1 ✓
CDK5 ✓
DCX ✓
DYNC1H1 ✓
FKRP ✓
FKTN ✓
FTO ✓
ISPD ✓
KATNB1 ✓
KIAA1279 ✓
KIF2A ✓
KIF5C ✓
LAMA2 ✓
LAMB1 ✓
LAMC3 ✓
LARGE ✓
NDE1 ✓
OCLN ✓
PAFAH1B1 ✓
PHGDH ✓
POMGNT1 ✓
POMGNT2 ✓
POMK ✓
POMT1 ✓
POMT2 ✓
RAB18 ✓
RAB3GAP1 ✓
RAB3GAP2 ✓
RELN ✓
RTTN ✓
SNAP29 ✓
SRD5A3 ✓
TBC1D20 ✓
TMEM5 ✓
TMTC3 ✓
TUBA1A ✓
TUBA8 ✓
TUBB ✓
TUBB2A ✓
TUBB2B ✓
TUBB3 ✓
TUBB4A ✓
TUBG1 ✓
VIPAS39 ✓
VLDLR ✓
VPS33B ✓
WDR62 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Macrocephaly and Overgrowth Syndrome gene Panel

MHL Testcode : GG117
Methodology : NGS
Disease Segment : Neurology
TAT : 21
Key genes :

+ Show Genes

×

ABCC9 ✓
ADK ✓
AKT1 ✓
AKT2 ✓
AKT3 ✓
ANKH ✓
ASPA ✓
ASXL2 ✓
BLTP1 ✓
BRSK2 ✓
BRWD3 ✓
CCND2 ✓
CDKN1C ✓
CHD3 ✓
CHD4 ✓
CHD8 ✓
CUL4B ✓
D2HGDH ✓
DHCR24 ✓
DICER1 ✓
DIS3L2 ✓
DNMT3A ✓
DVL1 ✓
EED ✓
EIF2B5 ✓
ERF ✓
ETFA ✓
ETFB ✓
ETFDH ✓
EXT2 ✓
EZH2 ✓
FBLN5 ✓
FBN1 ✓
FGFR3 ✓
FOXP1 ✓
GATAD2B ✓
GCDH ✓
GFAP ✓
GLI3 ✓
GPC3 ✓
GPC4 ✓
GPSM2 ✓
GRIA3 ✓
H1-4 ✓
H19 ✓
HEPACAM ✓
HERC1 ✓
HRAS ✓
HUWE1 ✓
KCNH1 ✓
KDM1A ✓
KIF7 ✓
KMT2E ✓
KPTN ✓
KRAS ✓
L1CAM ✓
LAMB1 ✓
LBR ✓
MED12 ✓
MITF ✓
MLC1 ✓
MPDZ ✓
MTM1 ✓
MTOR ✓
NF1 ✓
NFIA ✓
NFIB ✓
NFIX ✓
NONO ✓
NPR2 ✓
NRAS ✓
NSD1 ✓
ODC1 ✓
OFD1 ✓
PDGFRB ✓
PHF21A ✓
PHF6 ✓
PIGA ✓
PIGM ✓
PIK3CA ✓
PIK3R2 ✓
PPP1CB ✓
PPP2R5D ✓
PTCH1 ✓
PTEN ✓
RAB39B ✓
RIN2 ✓
RNF125 ✓
RNF135 ✓
SETD2 ✓
SHANK3 ✓
SHOC2 ✓
SNX14 ✓
SOS1 ✓
SPRED1 ✓
STRADA ✓
SUFU ✓
SUZ12 ✓
SYN1 ✓
SZT2 ✓
TBC1D7 ✓
TCF20 ✓
TGFB3 ✓
TMEM94 ✓
TRIO ✓
TRIP12 ✓
TSC1 ✓
TSC2 ✓
UPF3B ✓
WNT5A ✓
ZBTB20 ✓
ZBTB7A ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen MECP2 gene sequencing

MHL Testcode : GG118
Methodology : NGS
Disease Segment : Neurology
TAT : 26
Key genes :

+ Show Genes

×

MECP2 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Metabolic Epilepsy gene Panel

MHL Testcode : GG119
Methodology : NGS
Disease Segment : Neurology
TAT : 28
Key genes :

+ Show Genes

×

ABAT ✓
ADSL ✓
AGA ✓
ALDH5A1 ✓
ALDH7A1 ✓
AMT ✓
ARG1 ✓
BTD ✓
D2HGDH ✓
DHFR ✓
DNM1L ✓
DPYD ✓
DPYS ✓
ETFA ✓
ETFB ✓
ETFDH ✓
ETHE1 ✓
FH ✓
GAMT ✓
GCDH ✓
GCH1 ✓
GLDC ✓
GNE ✓
GPHN ✓
HIBCH ✓
L2HGDH ✓
MOCS1 ✓
MTHFR ✓
PGK1 ✓
PNPO ✓
POLG ✓
PRODH ✓
PTS ✓
QDPR ✓
SERAC1 ✓
SLC25A1 ✓
SLC25A15 ✓
SLC2A1 ✓
SLC39A8 ✓
SLC46A1 ✓
SUOX ✓
✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Metabolic Myopathy and Rhabdomyolysis gene Panel

MHL Testcode : GG120
Methodology : NGS
Disease Segment : Neurology
TAT : 21
Key genes :

+ Show Genes

×

ABHD5 ✓
ACAD9 ✓
ACADM ✓
ACADVL ✓
AGK ✓
AGL ✓
AHCY ✓
ALDOA ✓
AMACR ✓
AMPD1 ✓
ANO5 ✓
ATP2A1 ✓
ATP7B ✓
B3GALNT2 ✓
B4GAT1 ✓
C1QBP ✓
CACNA1S ✓
CAPN3 ✓
CASQ1 ✓
CAV3 ✓
CHAT ✓
CHKB ✓
COQ2 ✓
COQ4 ✓
COQ7 ✓
COQ8A ✓
COQ9 ✓
COX15 ✓
COX20 ✓
COX6B1 ✓
CPT1A ✓
CPT2 ✓
CTDP1 ✓
DAG1 ✓
DGUOK ✓
DMD ✓
DNA2 ✓
DNAJB6 ✓
DPM1 ✓
DPM2 ✓
DPM3 ✓
DYSF ✓
EMD ✓
ENO3 ✓
ETFA ✓
ETFB ✓
ETFDH ✓
FBXL4 ✓
FDX2 ✓
FHL1 ✓
FKRP ✓
FKTN ✓
FLAD1 ✓
GAA ✓
GATM ✓
GBE1 ✓
GFER ✓
GMPPB ✓
GYG1 ✓
GYS1 ✓
HADH ✓
HADHA ✓
HADHB ✓
HMBS ✓
ISCU ✓
ITGA7 ✓
LAMA2 ✓
LAMP2 ✓
LARGE1 ✓
LDHA ✓
LPIN1 ✓
MAN2B1 ✓
MGME1 ✓
MICU1 ✓
MPV17 ✓
MYH3 ✓
OPA1 ✓
OPA3 ✓
PDSS1 ✓
PDSS2 ✓
PFKM ✓
PGAM2 ✓
PGK1 ✓
PGM1 ✓
PHKA1 ✓
PHKB ✓
PNPLA2 ✓
PNPLA8 ✓
POLG ✓
POLG2 ✓
POMGNT1 ✓
POMGNT2 ✓
POMK ✓
POMT1 ✓
POMT2 ✓
PUS1 ✓
PYGM ✓
RBCK1 ✓
RNASEH1 ✓
RRM2B ✓
RXYLT1 ✓
RYR1 ✓
SCN4A ✓
SDHA ✓
SGCA ✓
SGCB ✓
SGCD ✓
SGCG ✓
SIL1 ✓
SLC16A1 ✓
SLC22A5 ✓
SLC25A20 ✓
SLC25A3 ✓
SLC25A4 ✓
SLC25A42 ✓
STAC3 ✓
SUCLA2 ✓
SUCLG1 ✓
TANGO2 ✓
TCAP ✓
TK2 ✓
TNPO3 ✓
TRIM32 ✓
TRMT5 ✓
TSFM ✓
TWNK ✓
TYMP ✓
YARS2 ✓
✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Metachromatic leukodystrophy gene panel

MHL Testcode : GG121
Methodology : NGS
Disease Segment : Neurology
TAT : 28
Key genes :

+ Show Genes

×

ARSA ✓
PSAP ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen MFSD8 gene sequencing

MHL Testcode : GG122
Methodology : NGS
Disease Segment : Neurology
TAT : 21
Key genes :

+ Show Genes

×

MFSD8 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Microcephaly and Pontocerebellar Hypoplasia gene Panel

MHL Testcode : GG123
Methodology : NGS
Disease Segment : Neurology
TAT : 28
Key genes :

+ Show Genes

×

AKT3 ✓
AMPD2 ✓
ASPM ✓
ASXL1 ✓
ASXL3 ✓
ATR ✓
CASK ✓
CCDC47 ✓
CDK5RAP2 ✓
CENPF ✓
CENPJ ✓
CEP152 ✓
CEP63 ✓
CSNK2A1 ✓
DONSON ✓
DYNC1H1 ✓
DYRK1A ✓
EFTUD2 ✓
EXOSC3 ✓
GFM1 ✓
GPT2 ✓
KANSL1* ✓
KATNB1 ✓
KIF11 ✓
LIG4 ✓
MBD5 ✓
MCPH1# ✓
MED17 ✓
MFSD2A ✓
MIPEP* ✓
MRE11A ✓
MYCN ✓
MYO18B ✓
NCAPD3 ✓
NDE1 ✓
NHEJ1 ✓
OPHN1 ✓
PAFAH1B1 ✓
PCDH12 ✓
PCLO ✓
PCNT ✓
PHGDH ✓
PLK4 ✓
PNKP ✓
POMT1 ✓
PQBP1 ✓
QARS ✓
RARS2 ✓
RTTN ✓
SEPSECS ✓
SLC1A4 ✓
SMARCA2 ✓
SMARCE1 ✓
SOX11 ✓
STAG2 ✓
STAMBP ✓
STIL ✓
TBC1D20 ✓
TBC1D23 ✓
THOC6 ✓
TMTC3 ✓
TOE1 ✓
TOP3A ✓
TRMT10A ✓
TSEN2# ✓
TSEN54 ✓
TUBB* ✓
TUBB2B#* ✓
TUBGCP4 ✓
TUBGCP6 ✓
UBE3B ✓
VARS ✓
VRK1 ✓
WDR62 ✓
WDR73 ✓
XRCC4 ✓
ZNF148 ✓
ZNF335 ✓
✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Migraine gene Panel

MHL Testcode : GG124
Methodology : NGS
Disease Segment : Neurology
TAT : 28
Key genes :

+ Show Genes

×

ANKLE2 ✓
ARFGEF2 ✓
ASPM ✓
ASXL3 ✓
ATR ✓
ATRX ✓
CASC5 ✓
CASK ✓
CDC6 ✓
CDK5RAP2 ✓
CDK6 ✓
CDKL5 ✓
CDT1 ✓
CENPE ✓
CENPJ ✓
CEP135 ✓
CEP152 ✓
CEP63 ✓
CIT ✓
CRIPT ✓
DIAPH1 ✓
DYRK1A ✓
FOXG1 ✓
IER3IP1 ✓
KATNB1 ✓
KIF11 ✓
LIG4 ✓
MCPH1 ✓
MECP2 ✓
MED17 ✓
MFSD2A ✓
MSMO1 ✓
NBN ✓
NDE1 ✓
NHEJ1 ✓
NIN ✓
ORC1 ✓
ORC4 ✓
ORC6 ✓
PCNT ✓
PHC1 ✓
PLK4 ✓
PNKP ✓
PPP1R15B ✓
QARS ✓
RAB18 ✓
RAB3GAP1 ✓
RAB3GAP2 ✓
RAD50 ✓
RBBP8 ✓
RTTN ✓
SASS6 ✓
SLC25A19 ✓
SLC2A1 ✓
SLC9A6 ✓
STAMBP ✓
STIL ✓
TBC1D20 ✓
TCF4 ✓
TRAPPC9 ✓
TRMT10A ✓
TSEN2 ✓
TSEN34 ✓
TSEN54 ✓
TUBGCP4 ✓
TUBGCP6 ✓
UBE3A ✓
WDFY3 ✓
WDR62 ✓
XRCC4 ✓
ZEB2 ✓
ZNF335 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Muscular dystrophy and congenital myopathy gene panel

MHL Testcode : GG125
Methodology : NGS
Disease Segment : Neurology
TAT : 28
Key genes :

+ Show Genes

×

ACTA1 ✓
ANO5 ✓
B3GALNT2 ✓
B4GAT1 ✓
BAG3 ✓
BIN1 ✓
BVES ✓
CAPN3 ✓
CAV3 ✓
CCDC78 ✓
CFL2 ✓
CHKB ✓
CNTN1 ✓
COL12A1 ✓
COL6A1 ✓
COL6A2 ✓
COL6A3 ✓
CRYAB ✓
DAG1 ✓
DES ✓
DMD ✓
DNAJB6 ✓
DNM2 ✓
DYSF ✓
EMD ✓
FHL1 ✓
FKRP ✓
FKTN ✓
FLNC ✓
GMPPB ✓
GNE ✓
HNRNPA2B1 ✓
HNRNPDL ✓
ISCU ✓
ISPD ✓
ITGA7 ✓
KBTBD13 ✓
KLHL40 ✓
KLHL41 ✓
LAMA2 ✓
LAMP2 ✓
LARGE ✓
LDB3 ✓
LIMS2 ✓
LMNA ✓
LMOD3 ✓
MEGF10 ✓
MTM1 ✓
MYF6 ✓
MYH2 ✓
MYH7 ✓
MYOT ✓
NEB ✓
PABPN1 ✓
PLEC ✓
POGLUT1 ✓
POMGNT1 ✓
POMGNT2 ✓
POMK ✓
POMT1 ✓
POMT2 ✓
RYR1 ✓
SEPN1 ✓
SGCA ✓
SGCB ✓
SGCD ✓
SGCG ✓
SMCHD1 ✓
SPEG ✓
SYNE1 ✓
SYNE2 ✓
TCAP ✓
TMEM43 ✓
TMEM5 ✓
TNNT1 ✓
TNPO3 ✓
TOR1AIP1 ✓
TPM2 ✓
TPM3 ✓
TRAPPC11 ✓
TRIM32 ✓
TTN ✓
VCP ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen MYH3 gene sequencing

MHL Testcode : GG126
Methodology : NGS
Disease Segment : Neurology
TAT : 28
Key genes :

+ Show Genes

×

MYH3 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Myotonia congenita , deletion and duplication analysis

MHL Testcode : GG127
Methodology : MLPA
Disease Segment : Neurology
TAT : 21
Key genes :

+ Show Genes

×

CLCN1 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Myotonia congenita gene panel

MHL Testcode : GG128
Methodology : NGS
Disease Segment : Neurology
TAT : 28
Key genes :

+ Show Genes

×

CLCN1 ✓
SCN4A ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen NCL and Progressive Myoclonic Epilepsy Panel

MHL Testcode : GG129
Methodology : NGS
Disease Segment : Neurology
TAT : 28
Key genes :

+ Show Genes

×

AFG3L2 ✓
ASAH1 ✓
ATP13A2 ✓
BRAT1 ✓
CERS1 ✓
CLN3 ✓
CLN5 ✓
CLN6 ✓
CLN8 ✓
CSTB ✓
CTSD ✓
CTSF ✓
DNAJC5 ✓
EPM2A ✓
FARS2 ✓
FOLR1 ✓
GABRB2 ✓
GOSR2 ✓
GRN ✓
KCNC1 ✓
KCTD7 ✓
MFSD8 ✓
NEU1 ✓
NHLRC1 ✓
POLG ✓
PPT1 ✓
PRICKLE1 ✓
SCARB2 ✓
SERPINI1 ✓
TBC1D24 ✓
TPP1 ✓
✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen NDUFS7 gene sequencing

MHL Testcode : GG130
Methodology : NGS
Disease Segment : Neurology
TAT : 28
Key genes :

+ Show Genes

×

NDUFS7 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Nemaline Myopathy gene Panel

MHL Testcode : GG131
Methodology : NGS
Disease Segment : Neurology
TAT : 28
Key genes :

+ Show Genes

×

ACTA1 ✓
CFL2 ✓
KBTBD13 ✓
KLHL40 ✓
KLHL41 ✓
LMOD3 ✓
NEB ✓
TNNT1 ✓
TPM2 ✓
TPM3 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Neurodegeneration due to cerebral folate transport deficiency , gene sequencing

MHL Testcode : GG132
Methodology : NGS
Disease Segment : Neurology
TAT : 28
Key genes :

+ Show Genes

×

FOLR1 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Neurodegeneration with brain iron accumulation 2B , deletion and duplication analysis

MHL Testcode : GG133
Methodology : MLPA
Disease Segment : Neurology
TAT : 21
Key genes :

+ Show Genes

×

PLA2G6 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Neurodegeneration with brain iron accumulation gene panel

MHL Testcode : GG134
Methodology : NGS
Disease Segment : Neurology
TAT : 28
Key genes :

+ Show Genes

×

ATP13A2 ✓
COASY ✓
C19orf12 ✓
CP ✓
DCAF17 ✓
FA2H ✓
FTL ✓
PANK2 ✓
PLA2G6 ✓
WDR45 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Neurofibromatosis , gene analysis

MHL Testcode : GG135
Methodology : NGS
Disease Segment : Neurology
TAT : 28
Key genes :

+ Show Genes

×

NF1 ✓
NF2 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Neurofibromatosis type 1 , deletion and duplication analysis

MHL Testcode : GG136
Methodology : MLPA
Disease Segment : Neurology
TAT : 21
Key genes :

+ Show Genes

×

NF1 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Neurofibromatosis type 1 , gene analysis

MHL Testcode : GG137
Methodology : NGS
Disease Segment : Neurology
TAT : 28
Key genes :

+ Show Genes

×

NF1 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Neurofibromatosis type 2 , deletion and duplication analysis

MHL Testcode : GG138
Methodology : MLPA
Disease Segment : Neurology
TAT : 21
Key genes :

+ Show Genes

×

NF1 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Neurofibromatosis type 2 , gene analysis

MHL Testcode : GG139
Methodology : NGS
Disease Segment : Neurology
TAT : 28
Key genes :

+ Show Genes

×

NF2 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Neuronal ceroid lipofuscinosis gene panel

MHL Testcode : GG140
Methodology : NGS
Disease Segment : Neurology
TAT : 28
Key genes :

+ Show Genes

×

ATP13A2 ✓
CLN3 ✓
CLN5 ✓
CLN6 ✓
CLN8 ✓
CTSD ✓
CTSF ✓
DNAJC5 ✓
GRN ✓
KCTD7 ✓
MFSD8 ✓
PPT1 ✓
TPP1 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Neuronal migration disorder gene panel

MHL Testcode : GG141
Methodology : NGS
Disease Segment : Neurology
TAT : 28
Key genes :

+ Show Genes

×

ACTB ✓
ACTG1 ✓
ADGRG1 ✓
AKT3 ✓
ARFGEF2 ✓
ARX ✓
B3GALNT2 ✓
B4GAT1 ✓
CCND2 ✓
CDK5 ✓
COL4A1 ✓
COL4A2 ✓
DCX ✓
DEPDC5 ✓
DYNC1H1 ✓
EMX2 ✓
ERMARD ✓
FAT4 ✓
FIG4 ✓
FKRP ✓
FKTN ✓
FLNA ✓
GMPPB ✓
ISPD ✓
KATNB1 ✓
KIAA1279 ✓
KIF2A ✓
KIF5C ✓
L1CAM ✓
LAMB1 ✓
LARGE ✓
MCPH1 ✓
NDE1 ✓
NEDD4L ✓
OCLN ✓
PAFAH1B1 ✓
PI4KA ✓
PIK3CA ✓
PIK3R2 ✓
POMGNT1 ✓
POMGNT2 ✓
POMK ✓
POMT1 ✓
POMT2 ✓
RELN ✓
RTTN ✓
SHH ✓
SIX3 ✓
SRPX2 ✓
TMEM5 ✓
TUBA1A ✓
TUBA8 ✓
TUBB ✓
TUBB2A ✓
TUBB2B ✓
TUBB3 ✓
TUBG1 ✓
WDR62 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Neuro-Ophthalmology gene Panel

MHL Testcode : GG142
Methodology : NGS
Disease Segment : Neurology
TAT : 28
Key genes :

+ Show Genes

×

ACO2 ✓
ANTXR1 ✓
APTX ✓
CHN1 ✓
CISD2 ✓
FDXR ✓
FRMD7 ✓
GPR143 ✓
HESX1 ✓
KIF21A ✓
MFN2 ✓
MTRFR ✓
NDUFS1 ✓
NR2F1 ✓
OPA1 ✓
OPA3 ✓
OTX2 ✓
PAX6 ✓
PHOX2A ✓
POLG ✓
PRPS1 ✓
ROBO3 ✓
RRM2B ✓
RTN4IP1 ✓
SALL4 ✓
SETX ✓
SLC25A4 ✓
SLC25A46 ✓
SLC38A8 ✓
SOX2 ✓
SPG7 ✓
TIMM8A ✓
TK2 ✓
TMEM126A ✓
TUBB3 ✓
TWNK ✓
TYMP ✓
WFS1 ✓
✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Neurotransmitter disorders gene panel

MHL Testcode : GG143
Methodology : NGS
Disease Segment : Neurology
TAT : 28
Key genes :

+ Show Genes

×

ABAT ✓
ALDH5A1 ✓
ALDH7A1 ✓
AMT ✓
ARHGEF9 ✓
ATP13A2 ✓
C19orf12 ✓
CACNA1A ✓
CACNA1S ✓
CACNB2 ✓
CACNB4 ✓
COASY ✓
DBH ✓
DDC ✓
DNAJC6 ✓
FBXO7 ✓
FTL ✓
GAD1 ✓
GCH1 ✓
GCSH ✓
GLDC ✓
GLRA1 ✓
GLRB ✓
GPHN ✓
KCNA1 ✓
LRRK2 ✓
MAOA ✓
MAOB ✓
PANK2 ✓
PARK2 ✓
PARK7 ✓
PCBD1 ✓
PHGDH ✓
PINK1 ✓
PLA2G6 ✓
PNPO ✓
PSAT1 ✓
PSPH ✓
PTS ✓
QDPR ✓
RAB39B ✓
SCN4A ✓
SLC18A2 ✓
SLC1A3 ✓
SLC25A22 ✓
SLC6A3 ✓
SLC6A5 ✓
SNCA ✓
SPR ✓
SYNJ1 ✓
TH ✓
VPS13C ✓
WDR45 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen NKX2-1 gene sequencing

MHL Testcode : GG144
Methodology : NGS
Disease Segment : Neurology
TAT : 28
Key genes :

+ Show Genes

×

NKX2-1 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen NOTCH3 , gene analysis

MHL Testcode : GG145
Methodology : NGS
Disease Segment : Neurology
TAT : 28
Key genes :

+ Show Genes

×

CADASIL ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen PANK2 gene sequencing

MHL Testcode : GG146
Methodology : NGS
Disease Segment : Neurology
TAT : 28
Key genes :

+ Show Genes

×

PANK2 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Pantothenate kinase-associated neurodegeneration , deletion and duplication analysis

MHL Testcode : GG147
Methodology : MLPA
Disease Segment : Neurology
TAT : 21
Key genes :

+ Show Genes

×

PANK2 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Parkinson Disease gene Panel

MHL Testcode : GG148
Methodology : NGS
Disease Segment : Neurology
TAT : 28
Key genes :

+ Show Genes

×

ATP13A2 ✓
ATP1A3 ✓
ATP7B ✓
C19ORF12 ✓
CHCHD10 ✓
CHCHD2 ✓
CP* ✓
CSF1R ✓
DCTN1 ✓
DNAJC12 ✓
DNAJC5 ✓
DNAJC6 ✓
FBXO7 ✓
FTL ✓
GBA* ✓
GCH1 ✓
GRN ✓
LRRK2 ✓
MAPT ✓
MT-ATP6 ✓
MT-ATP8 ✓
MT-CO1 ✓
MT-CO2 ✓
MT-CO3 ✓
MT-CYB ✓
MT-ND1 ✓
MT-ND2 ✓
MT-ND3 ✓
MT-ND4 ✓
MT-ND4L ✓
MT-ND5 ✓
MT-ND6 ✓
MT-RNR1 ✓
MT-RNR2 ✓
MT-TA ✓
MT-TC ✓
MT-TD ✓
MT-TE ✓
MT-TF ✓
MT-TG ✓
MT-TH ✓
MT-TI ✓
MT-TK ✓
MT-TL1 ✓
MT-TL2 ✓
MT-TM ✓
MT-TN ✓
MT-TP ✓
MT-TQ ✓
MT-TR ✓
MT-TS1 ✓
MT-TS2 ✓
MT-TT ✓
MT-TV ✓
MT-TW ✓
MT-TY ✓
NUS1* ✓
PANK2 ✓
PARK2 ✓
PARK7 ✓
PDE10A ✓
PDE8B ✓
PDGFB ✓
PDGFRB ✓
PINK1 ✓
PLA2G6 ✓
POLG ✓
PRKRA ✓
PSEN1 ✓
RAB39B ✓
SLC20A2 ✓
SLC30A10 ✓
SLC39A14# ✓
SLC6A3 ✓
SNCA ✓
SPR ✓
SYNJ1 ✓
TH ✓
VPS13A ✓
VPS13C ✓
VPS35* ✓
XPR1 ✓
✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Periodic Paralysis gene Panel

MHL Testcode : GG149
Methodology : NGS
Disease Segment : Neurology
TAT : 28
Key genes :

+ Show Genes

×

ATP1A2 ✓
CACNA1S ✓
KCNJ2 ✓
MCM3AP ✓
RYR1 ✓
SCN4A ✓
✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen PIEZO2 gene sequencing

MHL Testcode : GG150
Methodology : NGS
Disease Segment : Neurology
TAT : 28
Key genes :

+ Show Genes

×

PIEZO2 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen PLP1 gene sequencing

MHL Testcode : GG151
Methodology : NGS
Disease Segment : Neurology
TAT : 28
Key genes :

+ Show Genes

×

PLP1 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen PMP22 deletion and duplication analysis

MHL Testcode : GG152
Methodology : MLPA
Disease Segment : Neurology
TAT : 21
Key genes :

+ Show Genes

×

PMP22 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen PMP22 gene analysis ,

MHL Testcode : GG153
Methodology : NGS
Disease Segment : Neurology
TAT : 28
Key genes :

+ Show Genes

×

PMP22 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Polymicrogyria gene Panel

MHL Testcode : GG154
Methodology : NGS
Disease Segment : Neurology
TAT : 28
Key genes :

+ Show Genes

×

ADGRG1 ✓
AKT3 ✓
FH ✓
GPSM2 ✓
KIFBP ✓
LAMC3 ✓
NDE1 ✓
NSDHL ✓
OCLN ✓
RAB18 ✓
SRPX2 ✓
TUBA1A ✓
TUBA8 ✓
TUBB2A ✓
TUBB2B ✓
TUBB3 ✓
WDR62 ✓
✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Pontocerebellar hypoplasia gene panel

MHL Testcode : GG155
Methodology : NGS
Disease Segment : Neurology
TAT : 28
Key genes :

+ Show Genes

×

AMPD2 ✓
CASK ✓
CHMP1A ✓
CLP1 ✓
EXOSC3 ✓
EXOSC8 ✓
PCLO ✓
RARS2 ✓
SEPSECS ✓
TBC1D23 ✓
TOE1 ✓
TSEN15 ✓
TSEN2 ✓
TSEN34 ✓
TSEN54 ✓
VPS53 ✓
VRK1 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Porphyria gene Panel

MHL Testcode : GG156
Methodology : NGS
Disease Segment : Neurology
TAT : 28
Key genes :

+ Show Genes

×

ALAD ✓
ALAS2 ✓
CLPX ✓
CPOX ✓
FECH ✓
GATA1 ✓
HMBS ✓
PPOX ✓
UROD ✓
UROS ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen PRKN gene deletion and duplication analysis

MHL Testcode : GG157
Methodology : MLPA
Disease Segment : Neurology
TAT : 21
Key genes :

+ Show Genes

×

PRKN ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen PRKRA gene sequencing

MHL Testcode : GG158
Methodology : NGS
Disease Segment : Neurology
TAT : 28
Key genes :

+ Show Genes

×

PRKRA ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Progressive myoclonic epilepsy gene panel

MHL Testcode : GG159
Methodology : NGS
Disease Segment : Neurology
TAT : 28
Key genes :

+ Show Genes

×

ADRA2B ✓
ASAH1 ✓
ATP13A2 ✓
CERS1 ✓
CLN3 ✓
CLN5 ✓
CLN6 ✓
CLN8 ✓
CSTB ✓
CTSD ✓
CTSF ✓
DNAJC5 ✓
EPM2A ✓
FOLR1 ✓
GOSR2 ✓
GRN ✓
KCNC1 ✓
KCTD7 ✓
LMNB2 ✓
MFSD8 ✓
NEU1 ✓
NHLRC1 ✓
PPT1 ✓
PRDM8 ✓
PRICKLE1 ✓
PRICKLE2 ✓
SCARB2 ✓
TPP1 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen PSEN1 gene sequencing

MHL Testcode : GG160
Methodology : NGS
Disease Segment : Neurology
TAT : 28
Key genes :

+ Show Genes

×

PSEN1 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Pyridoxine-dependent epilepsy , gene analysis

MHL Testcode : GG161
Methodology : NGS
Disease Segment : Neurology
TAT : 28
Key genes :

+ Show Genes

×

ALDH7A1 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen RANBP2 gene sequencing

MHL Testcode : GG162
Methodology : NGS
Disease Segment : Neurology
TAT : 28
Key genes :

+ Show Genes

×

RANBP2 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Rett Syndrome , deletion and duplication analysis

MHL Testcode : GG163
Methodology : MLPA
Disease Segment : Neurology
TAT : 21
Key genes :

+ Show Genes

×

MECP2 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Rett Syndrome gene panel

MHL Testcode : GG164
Methodology : NGS
Disease Segment : Neurology
TAT : 28
Key genes :

+ Show Genes

×

CDKL5 ✓
FOXG1 ✓
MECP2 ✓
MEF2C ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen RSRC1 gene sequencing

MHL Testcode : GG165
Methodology : NGS
Disease Segment : Neurology
TAT : 28
Key genes :

+ Show Genes

×

RSRC1 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen SACS gene sequencing

MHL Testcode : GG166
Methodology : NGS
Disease Segment : Neurology
TAT : 28
Key genes :

+ Show Genes

×

SACS ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Sandhoff disease , gene sequencing

MHL Testcode : GG167
Methodology : NGS
Disease Segment : Neurology
TAT : 28
Key genes :

+ Show Genes

×

HEXB ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Septo-Optic Dysplasia Panel

MHL Testcode : GG168
Methodology : NGS
Disease Segment : Neurology
TAT : 28
Key genes :

+ Show Genes

×

GLI2 ✓
HESX1 ✓
HK1 ✓
OTX2 ✓
PAX6 ✓
PROP1 ✓
SOX2 ✓
SOX3 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen SETX gene sequencing

MHL Testcode : GG169
Methodology : NGS
Disease Segment : Neurology
TAT : 28
Key genes :

+ Show Genes

×

SETX ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen SMN and NAIP deletion and duplication analysis

MHL Testcode : GG170
Methodology : MLPA
Disease Segment : Neurology
TAT : 21
Key genes :

+ Show Genes

×

SMN and NAIP ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Spastic Paraplegia gene Panel

MHL Testcode : GG171
Methodology : NGS
Disease Segment : Neurology
TAT : 28
Key genes :

+ Show Genes

×

ABCD1 ✓
ACO2 ✓
ADAR ✓
AFG3L2 ✓
ALDH18A1 ✓
ALS2 ✓
AMPD2 ✓
AP4B1 ✓
AP4E1 ✓
AP4M1 ✓
AP4S1 ✓
AP5Z1 ✓
ARG1 ✓
ARL6IP1 ✓
ARSI ✓
ATL1 ✓
ATL3 ✓
ATP13A2 ✓
ATP2B4 ✓
ATRX ✓
B4GALNT1 ✓
BICD2 ✓
BSCL2 ✓
C19orf12 ✓
CAPN1 ✓
CCT5 ✓
CPT1C ✓
CYP27A1 ✓
CYP2U1 ✓
CYP7B1 ✓
DARS1 ✓
DDHD1 ✓
DDHD2 ✓
DSTYK ✓
ENTPD1 ✓
ERLIN1 ✓
ERLIN2 ✓
EXOSC3 ✓
FA2H ✓
FARS2 ✓
FLRT1 ✓
GAD1 ✓
GBA2 ✓
GCH1 ✓
GJC2 ✓
GM2A ✓
HACE1 ✓
HEXA ✓
HEXB ✓
HSPD1 ✓
IBA57 ✓
IFIH1 ✓
ITPR1 ✓
KDM5C ✓
KIDINS220 ✓
KIF1A ✓
KIF1C ✓
KIF5A ✓
L1CAM ✓
LYST ✓
MAG ✓
MARS1 ✓
MFN2 ✓
MTRFR ✓
NARS2 ✓
NIPA1 ✓
NT5C2 ✓
PGAP1 ✓
PLA2G6 ✓
PLP1 ✓
PNPLA6 ✓
POLR3A ✓
RAB3GAP2 ✓
REEP1 ✓
REEP2 ✓
RNF170 ✓
RTN2 ✓
SACS ✓
SARS2 ✓
SERAC1 ✓
SETX ✓
SLC16A2 ✓
SLC25A15 ✓
SLC33A1 ✓
SPART ✓
SPAST ✓
SPG11 ✓
SPG21 ✓
SPG7 ✓
SPTAN1 ✓
TECPR2 ✓
TFG ✓
TRPV4 ✓
TUBB4A ✓
UBAP1 ✓
UCHL1 ✓
UNC80 ✓
USP8 ✓
VAMP1 ✓
VCP ✓
VPS37A ✓
WASHC5 ✓
WDR48 ✓
ZFR ✓
ZFYVE26 ✓
ZFYVE27 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Spinal Muscular Atrophy , gene analysis

MHL Testcode : GG172
Methodology : Sanger Sequencing
Disease Segment : Neurology
TAT :
Key genes :

+ Show Genes

×

SMN1 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Spinal Muscular Atrophy , deletion and duplication analysis

MHL Testcode : GG173
Methodology : MLPA
Disease Segment : Neurology
TAT : 21
Key genes :

+ Show Genes

×

SMN1 ✓
SMN2 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Spinal Muscular Atrophy gene Panel

MHL Testcode : GG174
Methodology : NGS
Disease Segment : Neurology
TAT : 28
Key genes :

+ Show Genes

×

ASAH1 ✓
ASCC1 ✓
ATP7A ✓
BICD2 ✓
BSCL2 ✓
CHCHD10 ✓
DNAJB2 ✓
DYNC1H1 ✓
FBXO38 ✓
GARS ✓
HSPB8 ✓
IGHMBP2 ✓
LAS1L ✓
PLEKHG5 ✓
SIGMAR1 ✓
SLC5A7 ✓
TRPV4 ✓
TRIP4 ✓
UBA1 ✓
VAPB ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Spinocerebellar ataxia 1 , repeat expansion analysis

MHL Testcode : GG175
Methodology : Fragment Analysis
Disease Segment : Neurology
TAT :
Key genes :

+ Show Genes

×

ATXN1 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Spinocerebellar ataxia 12 , repeat expansion analysis

MHL Testcode : GG176
Methodology : Fragment Analysis
Disease Segment : Neurology
TAT :
Key genes :

+ Show Genes

×

PPP2R2B ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Spinocerebellar ataxia 2 , repeat expansion analysis

MHL Testcode : GG177
Methodology : Fragment Analysis
Disease Segment : Neurology
TAT :
Key genes :

+ Show Genes

×

ATXN2 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Spinocerebellar ataxia 3 , repeat expansion analysis

MHL Testcode : GG178
Methodology : Fragment Analysis
Disease Segment : Neurology
TAT :
Key genes :

+ Show Genes

×

ATXN3 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Spinocerebellar ataxia 6 , repeat expansion analysis

MHL Testcode : GG179
Methodology : Fragment Analysis
Disease Segment : Neurology
TAT :
Key genes :

+ Show Genes

×

CACNA1A ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Spinocerebellar ataxia 7 , repeat expansion analysis

MHL Testcode : GG180
Methodology : Fragment Analysis
Disease Segment : Neurology
TAT :
Key genes :

+ Show Genes

×

ATXN7 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Spinocerebellar ataxia repeat expansion analysis: SCA1, SCA2, SCA3, SCA6, SCA7,SCA12

MHL Testcode : GG181
Methodology : Fragment Analysis
Disease Segment : Neurology
TAT :
Key genes :

+ Show Genes

×

ATXN1 ✓
ATXN2 ✓
ATXN3 ✓
CACNA1A ✓
ATXN7 ✓
PPP2R2B ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen SPTBN2 gene sequencing

MHL Testcode : GG182
Methodology : NGS
Disease Segment : Neurology
TAT : 28
Key genes :

+ Show Genes

×

SPTBN2 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Tay-Sachs disease , deletion and duplication analysis

MHL Testcode : GG183
Methodology : MLPA
Disease Segment : Neurology
TAT : 21
Key genes :

+ Show Genes

×

HEXA ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Tay-Sachs disease , gene analysis

MHL Testcode : GG184
Methodology : NGS
Disease Segment : Neurology
TAT : 28
Key genes :

+ Show Genes

×

HEXA ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen TBC1D24 gene analysis

MHL Testcode : GG185
Methodology : NGS
Disease Segment : Neurology
TAT : 28
Key genes :

+ Show Genes

×

TBC1D24 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen TCF4 gene sequencing

MHL Testcode : GG186
Methodology : NGS
Disease Segment : Neurology
TAT : 28
Key genes :

+ Show Genes

×

TCF4 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen TIA1 and DES genes sequencing

MHL Testcode : GG187
Methodology : NGS
Disease Segment : Neurology
TAT : 28
Key genes :

+ Show Genes

×

TIA1 and DES ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Tuberous Sclerosis (TSC1 and TSC2) gene Panel

MHL Testcode : GG188
Methodology : NGS
Disease Segment : Neurology
TAT : 28
Key genes :

+ Show Genes

×

TSC1 ✓
TSC2 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen TSC1 deletion and duplication analysis

MHL Testcode : GG189
Methodology : MLPA
Disease Segment : Neurology
TAT : 21
Key genes :

+ Show Genes

×

TSC1 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen TSC2 deletion and duplication analysis

MHL Testcode : GG190
Methodology : MLPA
Disease Segment : Neurology
TAT : 21
Key genes :

+ Show Genes

×

TSC2 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen X-linked adrenoleukodystrophy , deletion and duplication analysis

MHL Testcode : GG191
Methodology : MLPA
Disease Segment : Neurology
TAT : 21
Key genes :

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ABCD1 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen X-linked Intellectual Disability gene Panel

MHL Testcode : GG192
Methodology : NGS
Disease Segment : Neurology
TAT : 28
Key genes :

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ABCD1 ✓
ACSL4 ✓
AFF2 ✓
AGTR2 ✓
AIFM1 ✓
ALG13 ✓
AMMECR1 ✓
AP1S2 ✓
ARHGEF6 ✓
ARHGEF9 ✓
ARSL ✓
ARX ✓
ATP6AP2 ✓
ATP7A ✓
ATRX ✓
BCAP31 ✓
BCOR ✓
BCORL1 ✓
BRWD3 ✓
CASK ✓
CCDC22 ✓
CDK16 ✓
CDKL5 ✓
CLCN4 ✓
CNKSR2 ✓
CUL4B ✓
DCX ✓
DDX3X ✓
DKC1 ✓
DLG3 ✓
DMD ✓
EBP ✓
EIF2S3 ✓
FAAH2 ✓
FAM50A ✓
FANCB ✓
FGD1 ✓
FLNA ✓
FMR1 ✓
FRMPD4 ✓
FTSJ1 ✓
GDI1 ✓
GK ✓
GPC3 ✓
GPKOW ✓
GRIA3 ✓
GRIPAP1 ✓
HCCS ✓
HCFC1 ✓
HDAC6 ✓
HDAC8 ✓
HMGB3 ✓
HNRNPH2 ✓
HPRT1 ✓
HSD17B10 ✓
HUWE1 ✓
IDS ✓
IGBP1 ✓
IKBKG ✓
IL1RAPL1 ✓
IQSEC2 ✓
KDM5C ✓
KDM6A ✓
KIF4A ✓
KLF8 ✓
KLHL15 ✓
L1CAM ✓
LAMP2 ✓
LAS1L ✓
MAOA ✓
MBTPS2 ✓
MECP2 ✓
MED12 ✓
MID1 ✓
MID2 ✓
MSL3 ✓
MTM1 ✓
NAA10 ✓
NDP ✓
NDUFA1 ✓
NEXMIF ✓
NHS ✓
NLGN3 ✓
NLGN4X ✓
NONO ✓
NSDHL ✓
OCRL ✓
OFD1 ✓
OGT ✓
OPHN1 ✓
OTC ✓
PAK3 ✓
PCDH19 ✓
PDHA1 ✓
PGK1 ✓
PHF6 ✓
PHF8 ✓
PIGA ✓
PLP1 ✓
POLA1 ✓
PORCN ✓
PQBP1 ✓
PRPS1 ✓
PTCHD1 ✓
RAB39B ✓
RBM10 ✓
RLIM ✓
RNF113A ✓
RPL10 ✓
RPS6KA3 ✓
SHROOM4 ✓
SLC16A2 ✓
SLC35A2 ✓
SLC6A8 ✓
SLC9A6 ✓
SLC9A7 ✓
SMC1A ✓
SMS ✓
SOX3 ✓
SRPX2 ✓
SSR4 ✓
STAG2 ✓
STEEP1 ✓
SYN1 ✓
SYP ✓
TAF1 ✓
THOC2 ✓
TIMM8A ✓
TMLHE ✓
TSPAN7 ✓
UBE2A ✓
UPF3B ✓
USP27X ✓
USP9X ✓
WDR45 ✓
ZC4H2 ✓
ZDHHC9 ✓
ZFP92 ✓
ZMYM3 ✓
ZNF674 ✓
ZNF711 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen X-linked spastic paraplegia-2 , deletion and duplication analysis

MHL Testcode : GG193
Methodology : MLPA
Disease Segment : Neurology
TAT : 21
Key genes :

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PLP1 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Abnormal genitalia and disorders of sex development panel

MHL Testcode : GG224
Methodology : NGS
Disease Segment : Endocrinology
TAT : 28
Key genes :

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AKR1C4 ✓
AMH ✓
AMHR2 ✓
ANOS1 ✓
AR ✓
ARL6 ✓
ARX ✓
ATF3 ✓
ATRX ✓
B3GLCT ✓
BBS1 ✓
BBS10 ✓
BBS12 ✓
BBS2 ✓
BBS4 ✓
BBS5 ✓
BBS7 ✓
BBS9 ✓
BCOR ✓
BMP15 ✓
BMP4 ✓
BMP7 ✓
BNC2 ✓
CBX2 ✓
CCNQ ✓
CDKN1C ✓
CEP41 ✓
CHD4 ✓
CHD7 ✓
CILK1 ✓
CREBBP ✓
CUL7 ✓
CYB5A ✓
CYP11A1 ✓
CYP11B1 ✓
CYP17A1 ✓
CYP19A1 ✓
DHCR24 ✓
DHCR7 ✓
DHH ✓
DMRT1 ✓
DMRT2 ✓
DNMT3B ✓
DYNC2H1 ✓
DYNC2I1 ✓
EFNB1 ✓
EPG5 ✓
ESCO2 ✓
EVC ✓
EVC2 ✓
FAT4 ✓
FBXL4 ✓
FEZF1 ✓
FGF10 ✓
FGF8 ✓
FGFR1 ✓
FGFR2 ✓
FGFR3 ✓
FIG4 ✓
FLNA ✓
FOXL2 ✓
FRAS1 ✓
FREM2 ✓
FSHB ✓
FSHR ✓
GATA4 ✓
GLI3 ✓
GNRH1 ✓
GNRHR ✓
GPC3 ✓
GRIP1 ✓
HBA1 ✓
HCCS ✓
HESX1 ✓
HFE ✓
HHAT ✓
HNF1B ✓
HOXA13 ✓
HOXA4 ✓
HOXB6 ✓
HS6ST1 ✓
HSD17B3 ✓
HSD17B4 ✓
HSD3B2 ✓
IL17RD ✓
INSL3 ✓
IRF6 ✓
KISS1 ✓
KISS1R ✓
LEP ✓
LEPR ✓
LHB ✓
LHCGR ✓
LHX3 ✓
LHX4 ✓
LMNA ✓
MAMLD1 ✓
MAP3K1 ✓
MCM9 ✓
MED12 ✓
MID1 ✓
MKKS ✓
MKS1 ✓
NEK1 ✓
NR0B1 ✓
NR3C1 ✓
NR5A1 ✓
NSMF ✓
OPHN1 ✓
PCNT ✓
PCSK1 ✓
PDE4D ✓
PEX1 ✓
PITX2 ✓
POR ✓
PROK2 ✓
PROKR2 ✓
PROP1 ✓
PSMC3IP ✓
PTDSS1 ✓
PTPN11 ✓
RBBP8 ✓
RIPK4 ✓
ROR2 ✓
RSPO1 ✓
SALL1 ✓
SEMA3A ✓
SETBP1 ✓
SOS1 ✓
SOX10 ✓
SOX2 ✓
SOX3 ✓
SOX9 ✓
SPECC1L ✓
SRD5A2 ✓
SRY ✓
STAR ✓
TAC3 ✓
TACR3 ✓
TBX15 ✓
TMEM70 ✓
TOE1 ✓
TP63 ✓
TRAIP ✓
TRIM32 ✓
TSPYL1 ✓
TTC8 ✓
TWIST2 ✓
UBR1 ✓
WDR11 ✓
WDR35 ✓
WNT4 ✓
WNT5A ✓
WNT7A ✓
WT1 ✓
WWOX ✓
ZEB2 ✓
ZFPM2 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Alstrom syndrome (ALMS1) gene analysis

MHL Testcode : GG225
Methodology : NGS
Disease Segment : Endocrinology
TAT : 28
Key genes :

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ALMS1 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Androgen receptor (AR) deletion/duplication analysis

MHL Testcode : GG226
Methodology : MLPA
Disease Segment : Endocrinology
TAT : 21
Key genes :

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AR ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Androgen receptor (AR) gene analysis

MHL Testcode : GG227
Methodology : NGS
Disease Segment : Endocrinology
TAT : 28
Key genes :

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AR ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Comprehensive monogenic diabetes gene panel

MHL Testcode : GG228
Methodology : NGS
Disease Segment : Endocrinology
TAT : 28
Key genes :

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ABCC8 ✓
AIRE ✓
AKT2 ✓
ALMS1 ✓
APPL1 ✓
BLK ✓
CISD2 ✓
CNOT1 ✓
CP ✓
DCAF17 ✓
DNAJC3 ✓
DYRK1B ✓
EIF2AK3 ✓
EIF2B1 ✓
EIF2S3 ✓
FOXP3 ✓
GATA4 ✓
GATA6 ✓
GCK ✓
GLIS3 ✓
HNF1A ✓
HNF1B ✓
HNF4A ✓
IER3IP1 ✓
IL2RA ✓
INS ✓
INSR ✓
ITCH ✓
KCNJ11 ✓
KLF11 ✓
LRBA ✓
MAFA ✓
NEUROD1 ✓
NEUROG3 ✓
NKX2-2 ✓
PAX4 ✓
PAX6 ✓
PCBD1 ✓
PDX1 ✓
PIK3R1 ✓
POLD1 ✓
PPP1R15B ✓
PTF1A ✓
RFX6 ✓
SLC19A2 ✓
SLC29A3 ✓
SLC2A2 ✓
STAT1 ✓
STAT3 ✓
TRMT10A ✓
WFS1 ✓
ZBTB20 ✓
ZFP57 ✓
ZMPSTE24 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Congenital adrenal hyperplasia CYP21A2 (21-0H) deletion/duplication analysis

MHL Testcode : GG229
Methodology : MLPA
Disease Segment : Endocrinology
TAT : 21
Key genes :

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CYP21A2 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Congenital adrenal hyperplasia CYP21A2 (21-0H) gene analysis

MHL Testcode : GG230
Methodology : NGS
Disease Segment : Endocrinology
TAT : 28
Key genes :

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CYP21A2 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Congenital adrenal hyperplasia due to 3-beta-hydroxysteroid dehydrogenase 2 deficiency (HSD3B2) gene analysis

MHL Testcode : GG231
Methodology : NGS
Disease Segment : Endocrinology
TAT : 28
Key genes :

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HSD3B2 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Congenital adrenal hyperplasia gene panel

MHL Testcode : GG232
Methodology : NGS
Disease Segment : Endocrinology
TAT : 28
Key genes :

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ARMC5 ✓
CYP11A1 ✓
CYP11B1* ✓
CYP11B2* ✓
CYP17A1 ✓
CYP21A2* ✓
HSD3B2 ✓
PDE11A ✓
PDE8B ✓
POR ✓
PRKAR1A ✓
STAR ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Congenital hypopituitarism gene panel

MHL Testcode : GG233
Methodology : NGS
Disease Segment : Endocrinology
TAT : 28
Key genes :

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CDON ✓
GLI2 ✓
GLI3 ✓
GPR161 ✓
HESX1 ✓
LHX3 ✓
LHX4 ✓
OTX2 ✓
PAX6 ✓
POU1F1 ✓
PROKR2 ✓
PROP1 ✓
SHH ✓
SIX3 ✓
SOX3 ✓
TGIF1 ✓
WDR11 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen CYP11B1 gene sequencing

MHL Testcode : GG234
Methodology : NGS
Disease Segment : Endocrinology
TAT : 28
Key genes :

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×

CYP11B1 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen GATA3 gene sequencing

MHL Testcode : GG235
Methodology : NGS
Disease Segment : Endocrinology
TAT : 28
Key genes :

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GATA3 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Glucocorticoid deficiency gene panel

MHL Testcode : GG236
Methodology : NGS
Disease Segment : Endocrinology
TAT : 28
Key genes :

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MC2R ✓
MRAP ✓
NNT ✓
NR3C1 ✓
POMC ✓
STAR ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Hereditary pancreatitis gene panel

MHL Testcode : GG237
Methodology : NGS
Disease Segment : Endocrinology
TAT : 28
Key genes :

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CFTR ✓
CTRC ✓
PRSS1 ✓
SPINK1 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen HNF1B gene sequencing

MHL Testcode : GG238
Methodology : NGS
Disease Segment : Endocrinology
TAT : 28
Key genes :

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HNF1B ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Hypercholesterolemia gene panel

MHL Testcode : GG239
Methodology : NGS
Disease Segment : Endocrinology
TAT : 28
Key genes :

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ABCA1 ✓
ABCG5 ✓
ABCG8 ✓
APOA1 ✓
APOA2 ✓
APOA5 ✓
APOB ✓
APOC2 ✓
APOC3 ✓
APOE ✓
CETP ✓
EPHX2 ✓
GHR ✓
GPIHBP1 ✓
ITIH4 ✓
LDLR ✓
LDLRAP1 ✓
LIPC ✓
LPL ✓
PCSK9 ✓
PPP1R17 ✓
SLCO1B1 ✓
SREBF2 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Hyperlipidemia gene panel

MHL Testcode : GG240
Methodology : NGS
Disease Segment : Endocrinology
TAT : 28
Key genes :

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×

ABCA1 ✓
ABCG5 ✓
ABCG8 ✓
ANGPTL3 ✓
APOA1 ✓
APOA5 ✓
APOB ✓
APOC2 ✓
CETP ✓
CREB3L3 ✓
CYP27A1 ✓
GPD1 ✓
GPIHBP1 ✓
LCAT ✓
LDLR ✓
LDLRAP1 ✓
LIPA ✓
LIPG ✓
LMF1 ✓
LPL ✓
LRP6 ✓
MTTP ✓
PCSK9 ✓
PNPLA2 ✓
SAR1B ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Hyperparathyroidism gene panel

MHL Testcode : GG241
Methodology : NGS
Disease Segment : Endocrinology
TAT : 28
Key genes :

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AIRE ✓
AP2S1 ✓
CASR ✓
CDC73 ✓
CDKN1A ✓
CDKN1B ✓
CDKN2B ✓
CDKN2C ✓
GCM2 ✓
GNA11 ✓
MEN1 ✓
PTH ✓
RET ✓
TRPV6 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Hypoglycemia, hyperinsulinism and ketone metabolism gene panel

MHL Testcode : GG242
Methodology : NGS
Disease Segment : Endocrinology
TAT : 28
Key genes :

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ABCC8 ✓
ACAT1 ✓
ACSF3 ✓
AGL ✓
ALDOA ✓
ALDOB ✓
ENO3 ✓
EPM2A ✓
FBP1 ✓
G6PC1 ✓
GAA ✓
GBE1 ✓
GCK ✓
GLUD1 ✓
GYG1 ✓
GYS1 ✓
GYS2 ✓
HADH ✓
HMGCL ✓
HMGCS2 ✓
HNF1A ✓
HNF4A ✓
INSR ✓
KCNJ11 ✓
LAMP2 ✓
LDHA ✓
MPV17 ✓
NHLRC1 ✓
OXCT1 ✓
PC ✓
PCK1 ✓
PDX1 ✓
PFKM ✓
PGAM2 ✓
PGK1 ✓
PGM1 ✓
PHKA1 ✓
PHKA2 ✓
PHKB ✓
PHKG2 ✓
PRKAG2 ✓
PRKAG3 ✓
PTF1A ✓
PYGL ✓
PYGM ✓
RBCK1 ✓
SLC16A1 ✓
SLC2A2 ✓
SLC37A4 ✓
UCP2 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Hypomagnesemia gene panel

MHL Testcode : GG243
Methodology : NGS
Disease Segment : Endocrinology
TAT : 28
Key genes :

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BSND ✓
CASR ✓
CLDN16 ✓
CLDN19 ✓
CNNM2 ✓
CNNM4 ✓
EGF ✓
EGFR ✓
FAM111A ✓
FXYD2 ✓
HNF1B ✓
KCNA1 ✓
KCNJ10 ✓
MAGT1 ✓
NIPA2 ✓
PCBD1 ✓
SARS2 ✓
SLC12A3 ✓
TRPM6 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Hypothyroidism and resistance to thyroid hormone gene panel

MHL Testcode : GG244
Methodology : NGS
Disease Segment : Endocrinology
TAT : 28
Key genes :

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DUOX2 ✓
DUOXA2 ✓
FOXE1 ✓
GNAS ✓
HESX1 ✓
IGSF1 ✓
NKX2-1 ✓
NKX2-5 ✓
PAX8 ✓
POU1F1 ✓
PROP1 ✓
SECISBP2 ✓
SLC16A2 ✓
SLC26A4 ✓
SLC5A5 ✓
TBL1X ✓
TG ✓
THRA ✓
THRB ✓
TPO ✓
TSHB ✓
TSHR ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Kallmann syndrome gene panel

MHL Testcode : GG245
Methodology : NGS
Disease Segment : Endocrinology
TAT : 28
Key genes :

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×

FGFR1 ✓
KAL1 ✓
PROK2 ✓
PROKR2 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Leptin deficiency (LEP) gene analysis

MHL Testcode : GG246
Methodology : NGS
Disease Segment : Endocrinology
TAT : 28
Key genes :

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×

LEP ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Maturity-Onset Diabetes of the Young (MODY) & neonatal diabetes gene panel

MHL Testcode : GG247
Methodology : NGS
Disease Segment : Endocrinology
TAT : 28
Key genes :

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×

ABCC8 ✓
AKT2 ✓
APPL1 ✓
BLK ✓
CEL ✓
CISD2 ✓
EIF2AK3 ✓
FOXP3 ✓
GCK ✓
GLIS3 ✓
GLUD1 ✓
HADH ✓
HNF1A ✓
HNF1B ✓
HNF4A ✓
IER3IP1 ✓
INS ✓
INSR ✓
KCNJ11 ✓
KLF11 ✓
MNX1 ✓
NEUROD1 ✓
NKX2-2 ✓
NKX6-1 ✓
PAX4 ✓
PDX1 ✓
PTF1A ✓
RFX6 ✓
SLC2A2 ✓
WFS1 ✓
ZFP57 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen MC4R gene sequencing

MHL Testcode : GG248
Methodology : NGS
Disease Segment : Endocrinology
TAT : 28
Key genes :

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×

MC4R ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen MCM6 gene sequencing

MHL Testcode : GG249
Methodology : NGS
Disease Segment : Endocrinology
TAT : 28
Key genes :

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×

MCM6 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen MKRN3 gene sequencing

MHL Testcode : GG250
Methodology : NGS
Disease Segment : Endocrinology
TAT : 28
Key genes :

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×

MKRN3 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Monogenic and syndromic obesity gene panel

MHL Testcode : GG251
Methodology : NGS
Disease Segment : Endocrinology
TAT : 28
Key genes :

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×

ALMS1 ✓
ARL6 ✓
BBS1 ✓
BBS10 ✓
BBS12 ✓
BBS2 ✓
BBS4 ✓
BBS5 ✓
BBS7 ✓
BBS9 ✓
CEP290 ✓
CREBBP ✓
CUL4B ✓
DYRK1B ✓
EP300 ✓
GNAS ✓
INPP5E ✓
KSR2 ✓
LEP ✓
LEPR ✓
MAGEL2 ✓
MC3R ✓
MC4R ✓
MEGF8 ✓
MKKS ✓
MKS1 ✓
NR0B2 ✓
NTRK2 ✓
PCNT ✓
PCSK1 ✓
PHF6 ✓
POMC ✓
PPARG ✓
PYY ✓
RAB23 ✓
RPS6KA3 ✓
SDCCAG8 ✓
SIM1 ✓
TBX3 ✓
TMEM67 ✓
TRIM32 ✓
TTC8 ✓
VPS13B ✓
WDPCP ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen NR0B1, ABCD1, AIRE gene sequencing

MHL Testcode : GG252
Methodology : NGS
Disease Segment : Endocrinology
TAT : 28
Key genes :

+ Show Genes

×

NR0B1 ✓
ABCD1 ✓
AIRE ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Premature ovarian failure gene panel

MHL Testcode : GG253
Methodology : NGS
Disease Segment : Endocrinology
TAT : 28
Key genes :

+ Show Genes

×

AIRE ✓
BMP15 ✓
CLPP ✓
CYP17A1 ✓
CYP19A1 ✓
EIF2B2 ✓
EIF2B4 ✓
EIF2B5 ✓
FIGLA ✓
FOXL2 ✓
FSHR ✓
GALT ✓
HFM1 ✓
LMNA ✓
MCM8 ✓
MCM9 ✓
NOBOX ✓
NR5A1 ✓
PSMC3IP ✓
SOHLH1 ✓
STAG3 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen Pseudohypoparathyroidism Ia (GNAS) gene sequencing

MHL Testcode : GG254
Methodology : NGS
Disease Segment : Endocrinology
TAT : 28
Key genes :

+ Show Genes

×

GNAS ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

MicroGen SRD5A2 gene analysis

MHL Testcode : GG255
Methodology : NGS
Disease Segment : Endocrinology
TAT : 28
Key genes :

+ Show Genes

×

SRD5A2 ✓
Specimen : Blood - 4 ml, EDTA
Shipping Conditions : Blood - 20-25°C

Alagille syndrome 1 (JAG1) deletion/duplication analysis

MHL Testcode : GG256
Methodology : MLPA
Disease Segment : Gastroenterology
TAT : 21
Key genes :

+ Show Genes

×

JAG1 ✓
Specimen : EDTA Blood-4ml
Shipping Conditions : Blood - 20-25°C

Alagille syndrome gene panel

MHL Testcode : GG257
Methodology : NGS
Disease Segment : Gastroenterology
TAT : 28
Key genes :

+ Show Genes

×

JAG1 ✓
NOTCH2 ✓
Specimen : EDTA Blood-4ml
Shipping Conditions : Blood - 20-25°C

Cholestasis gene panel

MHL Testcode : GG258
Methodology : NGS
Disease Segment : Gastroenterology
TAT : 28
Key genes :

+ Show Genes

×

ABCB11 ✓
ABCB4 ✓
ABCC2 ✓
ABCG5 ✓
ABCG8 ✓
ACOX2 ✓
AKR1D1 ✓
ALDOB ✓
AMACR ✓
ATP8B1 ✓
BAAT ✓
CC2D2A ✓
CFTR ✓
CLDN1 ✓
CYP27A1 ✓
CYP7B1 ✓
DCDC2 ✓
DGUOK ✓
DHCR7 ✓
FAH ✓
GNAS ✓
HNF1B ✓
HSD17B4 ✓
HSD3B7 ✓
JAG1 ✓
KMT2D ✓
LIPA ✓
MKS1 ✓
MPV17 ✓
MYO5B ✓
NOTCH2 ✓
NPC1 ✓
NPC2 ✓
NPHP1 ✓
NPHP3 ✓
NPHP4 ✓
NR1H4 ✓
PEX1 ✓
PEX10 ✓
PEX11B ✓
PEX12 ✓
PEX13 ✓
PEX14 ✓
PEX16 ✓
PEX19 ✓
PEX2 ✓
PEX26 ✓
PEX3 ✓
PEX5 ✓
PEX6 ✓
PEX7 ✓
PKD1L1 ✓
PKHD1 ✓
POLG ✓
SCYL1 ✓
SERPINA1 ✓
SLC10A1 ✓
SLC10A2 ✓
SLC25A13 ✓
SLC27A5 ✓
SLC51B ✓
SLCO1B3 ✓
SMPD1 ✓
TALDO1 ✓
TJP2 ✓
TMEM216 ✓
TRMU ✓
UGT1A1 ✓
VIPAS39 ✓
VPS33B ✓
Specimen : EDTA Blood-4ml
Shipping Conditions : Blood - 20-25°C

Congenital Diarrhea gene panel

MHL Testcode : GG259
Methodology : NGS
Disease Segment : Gastroenterology
TAT : 28
Key genes :

+ Show Genes

×

ADA ✓
ADAM17 ✓
AICDA ✓
ALG6 ✓
ANKZF1 ✓
ARPC1B ✓
BACH2 ✓
BTK ✓
C17orf62 ✓
CARD8 ✓
CARMIL2 ✓
CD3G ✓
CD40 ✓
CD40LG ✓
CD55 ✓
CTLA4 ✓
CYBA ✓
CYBB ✓
CYP27A1 ✓
DCLRE1C ✓
DEF6 ✓
DGAT1 ✓
DKC1 ✓
DOCK8 ✓
DUOX2 ✓
FCHO1 ✓
FOXP3 ✓
G6PC3 ✓
GUCY2C ✓
ICOS ✓
IL10 ✓
IL10RA ✓
IL10RB ✓
IL21 ✓
IL2RA ✓
IL2RB ✓
IL2RG ✓
ITGB2 ✓
JAK1 ✓
LCT ✓
LIG4 ✓
LIPA ✓
LRBA ✓
MEFV ✓
MVK ✓
MYO5B ✓
NCF2 ✓
NCF4 ✓
NEUROG3 ✓
NFAT5 ✓
NLRC4 ✓
NOD2 ✓
PIK3CD ✓
PIK3R1 ✓
PLCG2 ✓
POLA1 ✓
RAG1 ✓
RAG2 ✓
RIPK1 ✓
RTEL1 ✓
SAR1B ✓
SH2D1A ✓
SI ✓
SKIV2L ✓
SLC26A3 ✓
SLC37A4 ✓
SLC5A1 ✓
SLC9A3 ✓
SPINT2 ✓
STAT1 ✓
STAT3 ✓
STIM1 ✓
STX3 ✓
STXBP2 ✓
TGFB1 ✓
TGFBR1 ✓
TGFBR2 ✓
TTC37 ✓
TTC7A ✓
UNC45A ✓
WAS ✓
XIAP ✓
ZAP70 ✓
ZNF341 ✓
✓
Specimen : EDTA Blood-4ml
Shipping Conditions : Blood - 20-25°C

Congenital hepatic fibrosis gene panel

MHL Testcode : GG260
Methodology : NGS
Disease Segment : Gastroenterology
TAT : 28
Key genes :

+ Show Genes

×

AHI1 ✓
ANKS6 ✓
ARL13B ✓
ARL6 ✓
B9D1 ✓
B9D2 ✓
BBS1 ✓
BBS10 ✓
BBS12 ✓
BBS2 ✓
BBS4 ✓
BBS5 ✓
BBS7 ✓
BBS9 ✓
C5orf42 ✓
CC2D2A ✓
CEP164 ✓
CEP290 ✓
CEP41 ✓
EVC ✓
EVC2 ✓
GLIS2 ✓
IFT122 ✓
IFT80 ✓
INPP5E ✓
INVS ✓
IQCB1 ✓
KIF7 ✓
MKKS ✓
MKS1 ✓
NEK8 ✓
NPHP1 ✓
NPHP3 ✓
NPHP4 ✓
OFD1 ✓
PKD1 ✓
PKD2 ✓
PKHD1 ✓
RPGRIP1L ✓
TCTN1 ✓
TCTN2 ✓
TCTN3 ✓
TMEM138 ✓
TMEM216 ✓
TMEM231 ✓
TMEM237 ✓
TMEM67 ✓
TRIM32 ✓
TTC21B ✓
TTC8 ✓
WDR19 ✓
ZNF423 ✓
✓
Specimen : EDTA Blood-4ml
Shipping Conditions : Blood - 20-25°C

Gastrointestinal Atresia gene panel

MHL Testcode : GG261
Methodology : NGS
Disease Segment : Gastroenterology
TAT : 28
Key genes :

+ Show Genes

×

CDK9 ✓
CHD7 ✓
CLMP ✓
DHCR7 ✓
EFTUD2 ✓
FANCB ✓
FANCC ✓
GLI3 ✓
MYCN ✓
PTF1A ✓
RFX6 ✓
TTC7A ✓
Specimen : EDTA Blood-4ml
Shipping Conditions : Blood - 20-25°C

Gilbert syndrome (UGT1A1) gene analysis (only point mutation analysis)

MHL Testcode : GG262
Methodology : NGS
Disease Segment : Gastroenterology
TAT : 28
Key genes :

+ Show Genes

×

UGT1A1 ✓
Specimen : EDTA Blood-4ml
Shipping Conditions : Blood - 20-25°C

Hemochromatosis gene panel

MHL Testcode : GG263
Methodology : NGS
Disease Segment : Gastroenterology
TAT : 28
Key genes :

+ Show Genes

×

BMP2 ✓
FTH1 ✓
HAMP ✓
HFE ✓
HFE2 ✓
SLC40A1 ✓
TFR2 ✓
Specimen : EDTA Blood-4ml
Shipping Conditions : Blood - 20-25°C

Hirschsprung Disease gene panel

MHL Testcode : GG264
Methodology : NGS
Disease Segment : Gastroenterology
TAT : 28
Key genes :

+ Show Genes

×

BDNF ✓
CELSR3 ✓
EDN3 ✓
EDNRB ✓
KIF1BP ✓
L1CAM ✓
MITF ✓
NRG1 ✓
NRTN ✓
PAX3 ✓
PHOX2B ✓
RET ✓
RMRP ✓
SOX10 ✓
Specimen : EDTA Blood-4ml
Shipping Conditions : Blood - 20-25°C

Pancreatitis gene panel

MHL Testcode : GG265
Methodology : NGS
Disease Segment : Gastroenterology
TAT : 28
Key genes :

+ Show Genes

×

CASR ✓
CFTR ✓
CPA1 ✓
CTRC ✓
PRSS1 ✓
SPINK1 ✓
TRPV6 ✓
Specimen : EDTA Blood-4ml
Shipping Conditions : Blood - 20-25°C

Polycystic liver disease gene panel

MHL Testcode : GG266
Methodology : NGS
Disease Segment : Gastroenterology
TAT : 28
Key genes :

+ Show Genes

×

ALG8 ✓
GANAB ✓
LRP5 ✓
PKHD1 ✓
PRKCSH ✓
SEC63 ✓
Specimen : EDTA Blood-4ml
Shipping Conditions : Blood - 20-25°C

Progressive familial intrahepatic cholestasis gene panel

MHL Testcode : GG267
Methodology : NGS
Disease Segment : Gastroenterology
TAT : 28
Key genes :

+ Show Genes

×

ABCB11 ✓
ABCB4 ✓
ATP8B1 ✓
JAG1 ✓
NOTCH2 ✓
TJP2 ✓
Specimen : EDTA Blood-4ml
Shipping Conditions : Blood - 20-25°C

Progressive familial intrahepatic cholestasis-3 (ABCB4) deletion/duplication analysis

MHL Testcode : GG268
Methodology : MLPA
Disease Segment : Gastroenterology
TAT : 21
Key genes :

+ Show Genes

×

ABCBA4 ✓
Specimen : EDTA Blood-4ml
Shipping Conditions : Blood - 20-25°C

Tyrosinemia gene analysis

MHL Testcode : GG269
Methodology : NGS
Disease Segment : Gastroenterology
TAT : 28
Key genes :

+ Show Genes

×

FAH ✓
HPD ✓
TAT ✓
Specimen : EDTA Blood-4ml
Shipping Conditions : Blood - 20-25°C

UGT1A1 repeat analysis

MHL Testcode : GG270
Methodology : STR
Disease Segment : Gastroenterology
TAT : 14
Key genes :

+ Show Genes

×

UGT1A1 ✓
Specimen : EDTA Blood-4ml
Shipping Conditions : Blood - 20-25°C

Wilson disease (ATP7B) gene analysis

MHL Testcode : GG271
Methodology : NGS
Disease Segment : Gastroenterology
TAT : 28
Key genes :

+ Show Genes

×

ATP7B ✓
Specimen : EDTA Blood-4ml
Shipping Conditions : Blood - 20-25°C

All Tests

MicroGen Arrhythmogenic Right Ventricular Cardiomyopathy gene Panel - GG1

MicroGen Aorta gene Panel - GG2

MicroGen Arrhythmia gene Panel - GG3

MicroGen Atrial Fibrillation gene Panel - GG4

MicroGen Brugada Syndrome gene Panel - GG5

MicroGen Cardiac channelopathy gene panel - GG6

MicroGen Cardiomyopathy gene panel - GG7

MicroGen Cardiomyopathy predisposition - MYBPC3 - GG8

MicroGen Catecholaminergic Polymorphic Ventricular Tachycardia Panel - GG9

MicroGen Comprehensive Cardiology gene Panel - GG10

MicroGen Congenital Structural Heart Disease gene Panel - GG11

MicroGen Connective tissue disorder gene panel - GG12

MicroGen Coronary artery disease Polygenic Risk Test - GG13

MicroGen Cutis-laxa gene panel - GG14

MicroGen CYP2C19 Clopidogrel resistance - GG15

MicroGen Dilated Cardiomyopathy gene Panel - GG16

MicroGen Ehler Danlos syndrome gene panel - GG17

MicroGen Ehlers-Danlos syndrome type VI deletion/duplication analysis - GG18

MicroGen Fibrodysplasia ossificans progressive gene sequencing - GG19

MicroGen GDF1 and PKD1L1 gene sequencing - GG20

MicroGen Hereditary Hemorrhagic Telangiectasia gene Panel - GG21

MicroGen Hereditary Transthyretin-mediated amyloidosis TTR gene analysis - GG22

MicroGen Heterotaxy and Situs Inversus gene Panel - GG23

MicroGen Hypercholesterolemia gene panel - GG24

MicroGen Hyperlipidemia gene Panel - GG25

MicroGen Hypertrophic Cardiomyopathy gene Panel - GG26

MicroGen Left Ventricular Non-Compaction Cardiomyopathy gene Panel - GG27

MicroGen Liddle Syndrome gene Panel - GG28

MicroGen Long QT Syndrome gene Panel - GG29

MicroGen Marfan syndrome gene analysis - GG30

MicroGen Marfan Syndrome gene Panel - GG31

MicroGen Noonan and RASopathies gene panel - GG32

MicroGen Pulmonary Artery Hypertension gene Panel - GG33

MicroGen Short QT Syndrome gene Panel - GG34

MicroGen SHOX deletion/duplication analysis - GG35

MicroPlex Clopidogrel dosage CYP2C19*2 & CYP2C19*3 - GG36

MicroPlex Statin induced myopathy predisposition SLCO1B1 p.(Val174Ala) - GG37

MicroPlex Tangier Disease gene sequencing - GG38

MicroPlex Warfarin dosage-VKORC1 , CYP2C9*2,CYP2C9*3 - GG39

MicroGen Acute intermittent porphyria - HMBS gene analysis - GG195

MicroGen Adams-Oliver Syndrome gene panel - GG196

MicroGen Albinism gene panel - GG197

MicroGen ATP2A2 gene sequencing - GG198

MicroGen Cutis Laxa gene panel - GG199

MicroGen Dyskeratosis Congenita gene panel - GG200

MicroGen Ectodermal dysplasia gene panel - GG201

MicroGen EDA, EDAR, EDARADD gene analysis - GG202

MicroGen Ehlers-Danlos Syndrome gene panel - GG203

MicroGen Epidermolysis bullosa gene panel - GG204

MicroGen Erythropoietic protoporphyria-1 (FECH) gene sequencing - GG205

MicroGen Harlequin ichthyosis (ABCA12) gene analysis - GG206

MicroGen Hereditary Acrodermatitis Enteropathica gene panel - GG207

MicroGen Hereditary Melanoma and Skin Cancer gene panel - GG208

MicroGen Hermansky-Pudlak Syndrome gene panel - GG209

MicroGen Ichthyosis gene panel - GG210

MicroGen Kindler syndrome (FERMT1) gene sequencing - GG211

MicroGen KRT5 gene sequencing - GG212

MicroGen Neurofibromatosis gene panel - GG213

MicroGen Pachyonychia Congenita gene panel - GG214

MicroGen Palmoplantar Keratoderma gene panel - GG215

MicroGen PLEC gene sequencing - GG216

MicroGen Progeria and Progeroid Syndromes gene panel - GG217

MicroGen Sjogren-Larsson syndrome (ALDH3A2) gene analysis - GG218

MicroGen Tuberous Sclerosis gene panel - GG219

MicroGen TYR deletion/duplication analysis - GG220

MicroGen Waardenburg Syndrome gene panel - GG221

MicroGen Xeroderma pigmentosum gene panel - GG222

MicroGen ZMPSTE24 gene sequencing - GG223

MicroGen 4H syndrome gene panel - GG40

MicroGen ABCD1 gene analysis - GG41

MicroGen ADGRG1 gene sequencing - GG42

MicroGen Adrenoleukodystrophy , gene analysis - GG43

MicroGen ADSSL1 gene analysis - GG44

MicroGen Aicardi-Goutieres syndrome gene panel - GG45

MicroGen Alexander disease , gene analysis - GG46

MicroGen Alkaptonuria , gene analysis - GG47

MicroGen Amyotrophic Lateral Sclerosis gene panel - GG48

MicroGen Arthrogryposis and congenital myasthenic syndrome gene panel - GG49

MicroGen Ataxia-telangiectasia , deletion and duplication analysis - GG50

MicroGen Ataxia-telangiectasia , gene analysis - GG51

MicroGen ATP1A2 and ATP1A3 gene sequencing - GG52

MicroGen ATRX gene analysis - GG53

MicroGen Autism Spectrum Disorders gene panel , - GG54

MicroGen Autosomal dominant adult-onset demyelinating leukodystrophy , deletion and duplication analysis - GG55

MicroGen Benign infantile epilepsy gene panel - GG56

MicroGen Comprehensive Epilepsy gene Panel - GG57

MicroGen Brown Vialetto-Van Laere syndrome gene panel - GG58

MicroGen Calpainopathy and LGMD2A , deletion and duplication analysis - GG59

MicroGen Canavan disease , gene analysis - GG60

MicroGen CAPN3 gene sequencing - GG61

MicroGen Cerebral Cavernous Malformation gene Panel - GG62

MicroGen Charcot-Marie-Tooth 1A and HNPP , deletion and duplication analysis - GG63

MicroGen Charcot-Marie-Tooth and sensory neuropathies gene panel - GG64

MicroGen Charcot-Marie-Tooth type 4 , deletion and duplication analysis - GG65

MicroGen Charcot-Marie-Tooth type 4C , deletion and duplication analysis - GG66

MicroGen CLP1 gene sequencing - GG67

MicroGen Coenzyme q10 Deficiency gene panel - GG68

MicroGen Collagen Type VI-Related Disorders gene panel - GG69

MicroGen Congenital Muscular Dystrophy , deletion and duplication analysis - GG70

MicroGen Comprehensive neurology gene panel - GG71

MicroGen Congenital Myasthenic Syndromes gene Panel - GG72

MicroGen Creatine Metabolism Deficiency gene Panel - GG73

MicroGen CSTB gene sequencing - GG74

MicroGen Cystic megalencephaly , gene analysis - GG75

MicroGen Dementia gene Panel - GG76

MicroGen Dravet syndrome , deletion and duplication analysis - GG77

MicroGen Dravet syndrome , gene analysis - GG78

MicroGen Duchenne Muscular Dystrophy , deletion and duplication analysis - GG79

MicroGen Duchenne Muscular Dystrophy , gene sequencing - GG80

MicroGen DYSF gene sequencing - GG81

MicroGen Dysferlinopathy and LGMD2B , deletion and duplication analysis - GG82

MicroGen Dystonia gene panel - GG83

MicroGen Dystonia 28 , gene sequencing - GG84

MicroGen Early infantile epileptic encephalopathy-4 , deletion and duplication analysis - GG85

MicroGen Early-onset juvenile parkinsonism gene panel - GG86

MicroGen Emery-Dreifuss Muscular Dystrophy gene Panel - GG87

MicroGen Epileptic encephalopathy gene panel - GG88

MicroGen Episodic ataxia gene panel - GG89

MicroGen Familial female mental retardation and epilepsy gene panel - GG90

MicroGen Familial hemiplegic migraine gene panel - GG91

MicroGen Familial temporal lobe epilepsy-1 , gene sequencing - GG92

MicroGen Friedreich ataxia , - Repeat expansion analysis - GG93

MicroGen Fukuyama Congenital Muscular Dystrophy , gene sequencing , - GG94

MicroGen GAN and DCAF8 gene sequencing - GG95

MicroGen GBE1 gene sequencing - GG96

MicroGen GCH1 gene sequencing - GG97

MicroGen Giant axonal neuropathy-1 , gene analysis - GG98

MicroGen Gordon Holmes syndrome , gene sequencing - GG99

MicroGen Hereditary essential tremor , gene sequencing - GG100

MicroGen Hereditary spastic paraplegia gene panel - GG101

MicroGen HINT1 gene sequencing - GG102

MicroGen Holoprosencephaly gene Panel - GG103

MicroGen Huntington's disease , - Repeat expansion analysis - GG104

MicroGen Hyperekplexia gene panel - GG105

MicroGen Hypomyelination syndrome gene panel - GG106

MicroGen Idiopathic Generalized and Focal Epilepsy gene Panel - GG107

MicroGen IGHMBP2 gene sequencing - GG108

MicroGen Joubert syndrome gene panel - GG109

MicroGen KCNT1 gene sequencing - GG110

MicroGen Krabbe disease , deletion and duplication analysis - GG111

MicroGen Krabbe disease , gene analysis - GG112

MicroGen Leukodystrophy and Leukoencephalopathy gene Panel - GG113

MicroGen LGMD and Congenital Muscular Dystrophy gene Panel - GG114

MicroGen Lissencephaly gene panel - GG116

MicroGen Macrocephaly and Overgrowth Syndrome gene Panel - GG117

MicroGen MECP2 gene sequencing - GG118

MicroGen Metabolic Epilepsy gene Panel - GG119

MicroGen Metabolic Myopathy and Rhabdomyolysis gene Panel - GG120

MicroGen Metachromatic leukodystrophy gene panel - GG121

MicroGen MFSD8 gene sequencing - GG122

MicroGen Microcephaly and Pontocerebellar Hypoplasia gene Panel - GG123

MicroGen Migraine gene Panel - GG124

MicroGen Muscular dystrophy and congenital myopathy gene panel - GG125

MicroGen MYH3 gene sequencing - GG126

MicroGen Myotonia congenita , deletion and duplication analysis - GG127

MicroGen Myotonia congenita gene panel - GG128

MicroGen NCL and Progressive Myoclonic Epilepsy Panel - GG129

MicroGen NDUFS7 gene sequencing - GG130

MicroGen Nemaline Myopathy gene Panel - GG131

MicroGen Neurodegeneration due to cerebral folate transport deficiency , gene sequencing - GG132

MicroGen Neurodegeneration with brain iron accumulation 2B , deletion and duplication analysis - GG133

MicroGen Neurodegeneration with brain iron accumulation gene panel - GG134

MicroGen Neurofibromatosis , gene analysis - GG135

MicroGen Neurofibromatosis type 1 , deletion and duplication analysis - GG136

MicroGen Neurofibromatosis type 1 , gene analysis - GG137

MicroGen Neurofibromatosis type 2 , deletion and duplication analysis - GG138

MicroGen Neurofibromatosis type 2 , gene analysis - GG139

MicroGen Neuronal ceroid lipofuscinosis gene panel - GG140

MicroGen Neuronal migration disorder gene panel - GG141

MicroGen Neuro-Ophthalmology gene Panel - GG142

MicroGen Neurotransmitter disorders gene panel - GG143

MicroGen NKX2-1 gene sequencing - GG144

MicroGen NOTCH3 , gene analysis - GG145

MicroGen PANK2 gene sequencing - GG146

MicroGen Pantothenate kinase-associated neurodegeneration , deletion and duplication analysis - GG147

MicroGen Parkinson Disease gene Panel - GG148

MicroGen Periodic Paralysis gene Panel - GG149

MicroGen PIEZO2 gene sequencing - GG150

MicroGen PLP1 gene sequencing - GG151

MicroGen PMP22 deletion and duplication analysis - GG152

MicroGen PMP22 gene analysis , - GG153

MicroGen Polymicrogyria gene Panel - GG154

MicroGen Pontocerebellar hypoplasia gene panel - GG155

MicroGen Porphyria gene Panel - GG156

MicroGen PRKN gene deletion and duplication analysis - GG157

MicroGen PRKRA gene sequencing - GG158

MicroGen Progressive myoclonic epilepsy gene panel - GG159

MicroGen PSEN1 gene sequencing - GG160

MicroGen Pyridoxine-dependent epilepsy , gene analysis - GG161

MicroGen RANBP2 gene sequencing - GG162

MicroGen Rett Syndrome , deletion and duplication analysis - GG163

MicroGen Rett Syndrome gene panel - GG164

MicroGen RSRC1 gene sequencing - GG165

MicroGen SACS gene sequencing - GG166

MicroGen Sandhoff disease , gene sequencing - GG167

MicroGen Septo-Optic Dysplasia Panel - GG168

MicroGen SETX gene sequencing - GG169

MicroGen SMN and NAIP deletion and duplication analysis - GG170

MicroGen Spastic Paraplegia gene Panel - GG171

MicroGen Spinal Muscular Atrophy , gene analysis - GG172

MicroGen Spinal Muscular Atrophy , deletion and duplication analysis - GG173

MicroGen Spinal Muscular Atrophy gene Panel - GG174

MicroGen Spinocerebellar ataxia 1 , repeat expansion analysis - GG175

MicroGen Spinocerebellar ataxia 12 , repeat expansion analysis - GG176

MicroGen Spinocerebellar ataxia 2 , repeat expansion analysis - GG177

MicroGen Spinocerebellar ataxia 3 , repeat expansion analysis - GG178

MicroGen Spinocerebellar ataxia 6 , repeat expansion analysis - GG179

MicroGen Spinocerebellar ataxia 7 , repeat expansion analysis - GG180

MicroGen Spinocerebellar ataxia repeat expansion analysis: SCA1, SCA2, SCA3, SCA6, SCA7,SCA12 - GG181

MicroGen SPTBN2 gene sequencing - GG182

MicroGen Tay-Sachs disease , deletion and duplication analysis - GG183

MicroGen Tay-Sachs disease , gene analysis - GG184

MicroGen TBC1D24 gene analysis - GG185

MicroGen TCF4 gene sequencing - GG186

MicroGen TIA1 and DES genes sequencing - GG187

MicroGen Tuberous Sclerosis (TSC1 and TSC2) gene Panel - GG188

MicroGen TSC1 deletion and duplication analysis - GG189

MicroGen TSC2 deletion and duplication analysis - GG190

MicroGen X-linked adrenoleukodystrophy , deletion and duplication analysis - GG191

MicroGen X-linked Intellectual Disability gene Panel - GG192

MicroGen X-linked spastic paraplegia-2 , deletion and duplication analysis - GG193

MicroGen Abnormal genitalia and disorders of sex development panel - GG224

MicroGen Alstrom syndrome (ALMS1) gene analysis - GG225

MicroGen Androgen receptor (AR) deletion/duplication analysis - GG226

MicroGen Androgen receptor (AR) gene analysis - GG227

MicroGen Comprehensive monogenic diabetes gene panel - GG228

MicroGen Congenital adrenal hyperplasia CYP21A2 (21-0H) deletion/duplication analysis - GG229

MicroGen Congenital adrenal hyperplasia CYP21A2 (21-0H) gene analysis - GG230

MicroGen Congenital adrenal hyperplasia due to 3-beta-hydroxysteroid dehydrogenase 2 deficiency (HSD3B2) gene analysis - GG231

MicroGen Congenital adrenal hyperplasia gene panel - GG232

MicroGen Congenital hypopituitarism gene panel - GG233

MicroGen CYP11B1 gene sequencing - GG234

MicroGen GATA3 gene sequencing - GG235

MicroGen Glucocorticoid deficiency gene panel - GG236

MicroGen Hereditary pancreatitis gene panel - GG237

MicroGen HNF1B gene sequencing - GG238

MicroGen Hypercholesterolemia gene panel - GG239

MicroGen Hyperlipidemia gene panel - GG240

MicroGen Hyperparathyroidism gene panel - GG241

MicroGen Hypoglycemia, hyperinsulinism and ketone metabolism gene panel - GG242

MicroGen Hypomagnesemia gene panel - GG243

MicroGen Hypothyroidism and resistance to thyroid hormone gene panel - GG244

MicroGen Kallmann syndrome gene panel - GG245

MicroGen Leptin deficiency (LEP) gene analysis - GG246

MicroGen Maturity-Onset Diabetes of the Young (MODY) & neonatal diabetes gene panel - GG247

MicroGen MC4R gene sequencing - GG248

MicroGen MCM6 gene sequencing - GG249

MicroGen MKRN3 gene sequencing - GG250

MicroGen Monogenic and syndromic obesity gene panel - GG251

MicroGen NR0B1, ABCD1, AIRE gene sequencing - GG252

MicroGen Premature ovarian failure gene panel - GG253

MicroGen Pseudohypoparathyroidism Ia (GNAS) gene sequencing - GG254

MicroGen SRD5A2 gene analysis - GG255

Alagille syndrome 1 (JAG1) deletion/duplication analysis - GG256

Alagille syndrome gene panel - GG257

Cholestasis gene panel - GG258

Congenital Diarrhea gene panel - GG259

Congenital hepatic fibrosis gene panel - GG260

Gastrointestinal Atresia gene panel - GG261

Gilbert syndrome (UGT1A1) gene analysis (only point mutation analysis) - GG262

Hemochromatosis gene panel - GG263

Hirschsprung Disease gene panel - GG264

Pancreatitis gene panel - GG265

Polycystic liver disease gene panel - GG266

Progressive familial intrahepatic cholestasis gene panel - GG267

Progressive familial intrahepatic cholestasis-3 (ABCB4) deletion/duplication analysis - GG268

Tyrosinemia gene analysis - GG269

UGT1A1 repeat analysis - GG270

Wilson disease (ATP7B) gene analysis - GG271

Tests

MicroGen Arrhythmogenic Right Ventricular Cardiomyopathy gene Panel

MicroGen Aorta gene Panel

MicroGen Arrhythmia gene Panel

MicroGen Atrial Fibrillation gene Panel

MicroGen Brugada Syndrome gene Panel

MicroGen Cardiac channelopathy gene panel

MicroGen Cardiomyopathy gene panel

MicroGen Cardiomyopathy predisposition - MYBPC3

MicroGen Catecholaminergic Polymorphic Ventricular Tachycardia Panel

MicroGen Comprehensive Cardiology gene Panel

MicroGen Congenital Structural Heart Disease gene Panel

MicroGen Connective tissue disorder gene panel

MicroGen Coronary artery disease Polygenic Risk Test

MicroGen Cutis-laxa gene panel

MicroGen CYP2C19 Clopidogrel resistance

MicroGen Dilated Cardiomyopathy gene Panel

MicroGen Ehler Danlos syndrome gene panel

MicroGen Ehlers-Danlos syndrome type VI deletion/duplication analysis

MicroGen Fibrodysplasia ossificans progressive gene sequencing

MicroGen GDF1 and PKD1L1 gene sequencing

MicroGen Hereditary Hemorrhagic Telangiectasia gene Panel

MicroGen Hereditary Transthyretin-mediated amyloidosis TTR gene analysis

MicroGen Heterotaxy and Situs Inversus gene Panel

MicroGen Hypercholesterolemia gene panel

MicroGen Hyperlipidemia gene Panel

MicroGen Hypertrophic Cardiomyopathy gene Panel

MicroGen Left Ventricular Non-Compaction Cardiomyopathy gene Panel

MicroGen Liddle Syndrome gene Panel

MicroGen Long QT Syndrome gene Panel

MicroGen Marfan syndrome gene analysis

MicroGen Marfan Syndrome gene Panel

MicroGen Noonan and RASopathies gene panel

MicroGen Pulmonary Artery Hypertension gene Panel

MicroGen Short QT Syndrome gene Panel

MicroGen SHOX deletion/duplication analysis

MicroPlex Clopidogrel dosage CYP2C19*2 & CYP2C19*3

MicroPlex Statin induced myopathy predisposition SLCO1B1 p.(Val174Ala)

MicroPlex Tangier Disease gene sequencing

MicroPlex Warfarin dosage-VKORC1 , CYP2C9*2,CYP2C9*3

MicroGen Acute intermittent porphyria - HMBS gene analysis

MicroGen Adams-Oliver Syndrome gene panel

MicroGen Albinism gene panel

MicroGen ATP2A2 gene sequencing

MicroGen Cutis Laxa gene panel

MicroGen Dyskeratosis Congenita gene panel

MicroGen Ectodermal dysplasia gene panel

MicroGen EDA, EDAR, EDARADD gene analysis

MicroGen Ehlers-Danlos Syndrome gene panel

MicroGen Epidermolysis bullosa gene panel

MicroGen Erythropoietic protoporphyria-1 (FECH) gene sequencing

MicroGen Harlequin ichthyosis (ABCA12) gene analysis

MicroGen Hereditary Acrodermatitis Enteropathica gene panel

MicroGen Hereditary Melanoma and Skin Cancer gene panel

MicroGen Hermansky-Pudlak Syndrome gene panel

MicroGen Ichthyosis gene panel

MicroGen Kindler syndrome (FERMT1) gene sequencing

MicroGen KRT5 gene sequencing

MicroGen Neurofibromatosis gene panel

MicroGen Pachyonychia Congenita gene panel

MicroGen Palmoplantar Keratoderma gene panel

MicroGen PLEC gene sequencing

MicroGen Progeria and Progeroid Syndromes gene panel

MicroGen Sjogren-Larsson syndrome (ALDH3A2) gene analysis

MicroGen Tuberous Sclerosis gene panel

MicroGen TYR deletion/duplication analysis

MicroGen Waardenburg Syndrome gene panel

MicroGen Xeroderma pigmentosum gene panel

MicroGen ZMPSTE24 gene sequencing

MicroGen 4H syndrome gene panel

MicroGen ABCD1 gene analysis

MicroGen ADGRG1 gene sequencing

MicroGen Adrenoleukodystrophy , gene analysis

MicroGen ADSSL1 gene analysis

MicroGen Aicardi-Goutieres syndrome gene panel

MicroGen Alexander disease , gene analysis

MicroGen Alkaptonuria , gene analysis

MicroGen Amyotrophic Lateral Sclerosis gene panel

MicroGen Arthrogryposis and congenital myasthenic syndrome gene panel

MicroGen Ataxia-telangiectasia , deletion and duplication analysis

MicroPlex Clopidogrel dosage CYP2C192 & CYP2C193

MicroPlex Warfarin dosage-VKORC1 , CYP2C92,CYP2C93