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CHRNG

Methodik Next Generation Sequencing (NGS)

Parallele Sequenzierung mehrerer Gene


Dauer 3-6 Wochen

Material 2-4 ml EDTA-Blut
OMIM 100730

Gen-Panel-Analysen, die CHRNG enthalten

Carrier Screening - Couple ID 164.03 | >25kb

Gen Panel (617 Gene )

RLBP1
RMRP
BCS1L
RPE65
RS1
SACS
SC5D
BLM
SCN2A
SCN8A
SCNN1A
SCNN1B
SCNN1G
SCO2
SFTPB
SFTPC
SGCA
SGCB
SGCD
SGCG
SGSH
SH2D1A
ST3GAL5
SLC12A1
SLC12A3
SLC12A6
SLC16A1
SLC16A2
SLC17A5
SLC22A5
SLC25A13
SLC25A15
SLC26A2
SLC2A1
SLC34A2
SLC35A1
SLC35A3
SLC3A1
SLC4A1
SLC5A5
SLC6A8
SLC7A7
SLC7A9
SLC9A6
SMARCAL1
SMN1
SMPD1
SNAP29
BTD
SPR
SRD5A2
BTK
STAR
SUCLG1
SUOX
TAT
TAZ
TBCE
C10orf2
TCIRG1
TFR2
TG
TGM1
TH
TIMM8A
TK2
ACOX1
TNFRSF11B
CD40LG
TNNT1
MED12
TPO
TREX1
TRHR
TSFM
TSHB
TSHR
TSPYL1
TTN
TTPA
TYR
TYRP1
UBA1
UGT1A1
UQCRB
UROS
USH1C
USH2A
CLRN1
VDR
VLDLR
VPS33B
VRK1
WAS
FOXN1
WNT3
WNT7A
WRN
WT1
XPA
XPC
ZIC3
ZMPSTE24
DUOX2
MCOLN1
NPHS2
ADAMTS13
AAAS
CA2
CDH23
GFM1
PRX
NEUROG3
WNT10A
MRPS16
SLC25A20
RAB23
MRPS22
NPC2
VPS45
ADAMTSL2
ABCA12
PCDH15
CAPN3
CASR
CBS
PUS1
HPS3
HAMP
LRPPRC
HPS4
RTEL1
NDUFAF5
SAMHD1
APTX
SEPN1
USH1G
TRIM32
SLC4A11
SLC45A2
BSND
CD3D
MCEE
CD3E
UBR1
ADCK3
HAX1
RAB3GAP1
MLC1
SLC39A4
RAB3GAP2
PLCE1
ADGRV1
GJC2
DCLRE1C
PDSS1
INVS
EXOSC3
NAGS
FKRP
ARX
ALG1
HSD3B7
ATP6V0A2
ADA
LDLRAP1
DNAI2
CFTR
MMAA
VPS13A
NPHP4
FGD4
PSAT1
POMGNT1
FRAS1
P3H1
MMAB
CHM
SBDS
CHRNA1
CHRND
CHRNE
CHRNG
LYST
POMT2
EVC2
VSX2
SLC25A22
TECPR2
RDH12
SLC35C1
CLDN1
SUMF1
CLDN19
BRIP1
DHDDS
TPP1
CLN3
CLN5
CLN6
CLN8
SLC35D1
IYD
GTF2H5
PDHX
RARS2
INPP5E
ACAD9
CNGB3
EYS
AHI1
NHLRC1
OSTM1
CERKL
ANTXR2
ADAMTS2
VPS13B
COL11A2
COL17A1
KCTD7
COL1A2
COL4A3
COL4A4
COL4A5
COL7A1
FAM20C
COL27A1
GNPTG
LMBRD1
PDSS2
ALG6
ZNF469
CPS1
CPT1A
ETHE1
CPT2
DOLK
CRB1
TTC37
CRLF1
GNE
MED17
CRTAP
MMACHC
FAM126A
SIL1
CSTB
G6PC3
MOGS
TMEM216
HOGA1
CTNS
MMADHC
COQ2
CTSC
CTSD
CTSK
FREM2
TRMU
VPS53
OFD1
CYBA
CYBB
FAM161A
CYP11A1
CYP11B1
CYP11B2
CYP17A1
CYP19A1
CYP1B1
CYP27A1
CYP27B1
BBS10
LOXHD1
HGSNAT
HYLS1
DOK7
BBS12
DBT
ACE
DCX
DDB2
DDC
ESCO2
ACSF3
TSEN54
D2HGDH
TMEM67
MFSD8
DGUOK
DHCR24
DHCR7
DKC1
IQCB1
DLD
CEP290
DLL3
PLEKHG5
RPGRIP1L
DMD
DMP1
DNAH5
DNAI1
UQCRQ
MESP2
GNPTAB
DNMT3B
DPAGT1
DPM1
DPYD
SLC26A3
PREPL
PNPO
PRRT2
DSP
DNAJC19
SEPSECS
STRA6
DYSF
TYMP
EDA
EDN3
AGA
EDNRB
LCA5
AGL
EFEMP2
EGR2
EIF2AK3
EIF2B5
DUOXA2
AGPS
AGT
EMD
ENPP1
AGTR1
EPB42
ABCA4
AGXT
EPM2A
ERBB3
ERCC2
ERCC3
ERCC4
ERCC5
ERCC6
ERCC8
ETFA
ETFB
ETFDH
EVC
F11
F8
F9
FAH
FANCA
FANCB
FANCC
FANCG
AIRE
FBLN5
FBP1
FKTN
FGA
FGB
FGG
FH
ATP8B1
FLNA
FMR1
FOLR1
AKR1D1
FUCA1
ALDH3A2
G6PC
G6PD
SLC37A4
GAA
ALDH5A1
GALC
GALE
GALK1
GALNS
GALT
GAMT
ALDOB
GATA1
GATM
GBA
GBE1
GCDH
GCH1
GCK
ABCB11
GCSH
GDF5
GJA1
ALMS1
GJB1
GJB2
GLA
GLB1
GLDC
GLE1
GLI3
ALPL
GNS
ALS2
GP1BA
GP9
AMACR
ADGRG1
GRHPR
GSS
AMH
AMHR2
GUCY2D
GUSB
GYS2
AMT
HADH
HSD17B10
HADHA
HADHB
HBA1
HBA2
HBB
HESX1
HEXA
HEXB
HFE2
HGD
HIBCH
ANK1
HLCS
HMGCL
HMGCS2
HPD
HPRT1
HPS1
HSD17B3
HSD17B4
HSD3B2
HSPG2
HYAL1
IDS
IDUA
SP110
IGBP1
IGF1
IGHMBP2
ABCC8
IGSF1
IKBKAP
IKBKG
IL2RG
IL7R
INS
INSR
ABCD1
FOXP3
ITGA6
ITGB4
IVD
JAG1
JAK3
KCNJ1
KCNJ11
KCNQ1
KCNQ2
AQP2
L1CAM
LAMA2
LAMA3
LAMB2
LAMB3
LAMC2
LARGE1
LBR
LDLR
LHCGR
LHX3
LIFR
LIPA
ARG1
LMNA
LPL
LRP2
LRP5
MAN2B1
MAT1A
MCCC1
MCCC2
MEFV
MGAT2
CIITA
MKS1
ARSA
ARSB
MLYCD
ARSE
MOCS1
MOCS2
MPI
MPL
MPV17
MPZ
MTHFR
MTM1
ASL
MTTP
MTR
MTRR
TRIM37
MUT
MUTYH
ASNS
MVK
ASPA
ASS1
MYO15A
MYO5A
MYO7A
NAGA
NAGLU
NBN
NDP
NDRG1
NDUFS6
NEB
NEU1
NPC1
NPHP1
NPHP3
NPHS1
ATIC
ATM
NR0B1
NR2E3
NTRK1
NUP62
OAT
OCRL
OPA3
OTC
ATP6V1B1
PAH
PAX6
PAX8
PC
PCBD1
PCCA
PCCB
ATP7A
ATP7B
ALDH7A1
PDHA1
PDHB
SLC26A4
ATR
PEX1
PEX10
PEX6
ATRX
PEX7
CFP
PFKM
ACADM
AUH
PHGDH
PHKB
SERPINA1
AVPR2
ACADS
PKHD1
PKLR
PLA2G6
PLEC
PLG
PLOD1
PLP1
ACADSB
PMM2
PMP22
POLG
ACADVL
POMT1
POR
POU1F1
B4GALT1
PDP1
ACAT1
PPT1
PQBP1
PROC
PROP1
PRPS1
PSAP
PTH1R
BBS1
PTPRC
BBS2
PTS
PEX2
PYGL
PYGM
QDPR
RAB27A
BCHE
RAG1
RAG2
BCKDHA
RAPSN
BCKDHB
RB1
RELN
REN
Fetale Akinesie / Arthrogryposis Multiplex Congenita (AMC) ID 078.03 | >25kb

Gen Panel (189 Gene )

RYR1
BIN1
SCN4A
AIMP1
SGCA
SGCB
SGCD
SGCG
SLC22A5
SLC25A1
SLC35A3
SNAP25
SYT2
TCAP
TGFBR2
TK2
TNNI2
TNNT1
TNNT3
TPM2
TPM3
TRIP4
MYOT
TTN
TUBB2A
UBA1
VPS33B
ZMPSTE24
ACTA1
ACTB
LPIN1
TMEM5
ADGRG6
CCDC78
ACTG1
CAPN3
DNAJB6
CAV3
TSEN34
B4GAT1
LDB3
GDAP1
SEPN1
SLC52A3
TRIM32
MFN2
SPEG
KLHL41
SYNE2
SYNE1
BICD2
RRM2B
EXOSC3
FKRP
TRPV4
FKBP10
NEK9
FKBP14
CFL2
NALCN
CHAT
POMGNT1
CHKB
CHRNA1
CHRNB1
CHRND
CHRNE
CHRNG
POMT2
VIPAS39
SLC25A26
ABHD5
CNTN1
COL13A1
VMA21
COL6A1
COL6A2
COL6A3
FAM20C
COLQ
GMPPB
ALG2
CPT2
GNE
ADCY6
CRYAB
ASCC1
CHST14
SIL1
ZC4H2
CTDP1
CUL4B
LAS1L
POMGNT2
POMK
PIEZO2
DOK7
IBA57
ANO5
TSEN54
DES
ALG14
TSEN2
TMEM43
B3GALNT2
ADSL
DMD
DYNC1H1
DYNC2H1
MEGF10
DNM2
ISCU
DPAGT1
DPM2
KLHL40
SEPSECS
PNPLA2
TUBB2B
DYSF
TOR1A
ECEL1
AGL
EGR2
ZBTB42
AGRN
EMD
ERBB3
ERCC6
ETFA
ETFB
ETFDH
FBN2
FKTN
FGFR2
FHL1
KBTBD13
ISPD
FLNB
FLNC
GAA
GARS
GBA
GBE1
GFPT1
GLE1
HADH
HADHA
HADHB
RIPK4
HRAS
HSPG2
IGHMBP2
FOXP3
ITGA7
LAMA2
LAMB2
LAMP2
LARGE1
LMNA
LMOD3
MAGEL2
MATR3
MPZ
MTM1
MTMR1
MUSK
MYBPC1
MYH2
MYH3
MYH7
MYH8
MYO9A
MYOD1
NEB
NEFL
CNTNAP1
PFKM
ACADM
PHGDH
PIP5K1C
ACADS
PLEC
PLOD2
POLG
ACADVL
POMT1
BAG3
PYGM
RAPSN
Fetale Akinesie / Arthrogryposis Multiplex Congenita (AMC) ID 078.03 | >25kb

Gen Panel (189 Gene )

RYR1
BIN1
SCN4A
AIMP1
SGCA
SGCB
SGCD
SGCG
SLC22A5
SLC25A1
SLC35A3
SNAP25
SYT2
TCAP
TGFBR2
TK2
TNNI2
TNNT1
TNNT3
TPM2
TPM3
TRIP4
MYOT
TTN
TUBB2A
UBA1
VPS33B
ZMPSTE24
ACTA1
ACTB
LPIN1
TMEM5
ADGRG6
CCDC78
ACTG1
CAPN3
DNAJB6
CAV3
TSEN34
B4GAT1
LDB3
GDAP1
SEPN1
SLC52A3
TRIM32
MFN2
SPEG
KLHL41
SYNE2
SYNE1
BICD2
RRM2B
EXOSC3
FKRP
TRPV4
FKBP10
NEK9
FKBP14
CFL2
NALCN
CHAT
POMGNT1
CHKB
CHRNA1
CHRNB1
CHRND
CHRNE
CHRNG
POMT2
VIPAS39
SLC25A26
ABHD5
CNTN1
COL13A1
VMA21
COL6A1
COL6A2
COL6A3
FAM20C
COLQ
GMPPB
ALG2
CPT2
GNE
ADCY6
CRYAB
ASCC1
CHST14
SIL1
ZC4H2
CTDP1
CUL4B
LAS1L
POMGNT2
POMK
PIEZO2
DOK7
IBA57
ANO5
TSEN54
DES
ALG14
TSEN2
TMEM43
B3GALNT2
ADSL
DMD
DYNC1H1
DYNC2H1
MEGF10
DNM2
ISCU
DPAGT1
DPM2
KLHL40
SEPSECS
PNPLA2
TUBB2B
DYSF
TOR1A
ECEL1
AGL
EGR2
ZBTB42
AGRN
EMD
ERBB3
ERCC6
ETFA
ETFB
ETFDH
FBN2
FKTN
FGFR2
FHL1
KBTBD13
ISPD
FLNB
FLNC
GAA
GARS
GBA
GBE1
GFPT1
GLE1
HADH
HADHA
HADHB
RIPK4
HRAS
HSPG2
IGHMBP2
FOXP3
ITGA7
LAMA2
LAMB2
LAMP2
LARGE1
LMNA
LMOD3
MAGEL2
MATR3
MPZ
MTM1
MTMR1
MUSK
MYBPC1
MYH2
MYH3
MYH7
MYH8
MYO9A
MYOD1
NEB
NEFL
CNTNAP1
PFKM
ACADM
PHGDH
PIP5K1C
ACADS
PLEC
PLOD2
POLG
ACADVL
POMT1
BAG3
PYGM
RAPSN

Einzelgenanalyse

Assoziierte Erkrankung(en)