Gen-Panel
Hereditäre Neuropathien, umfassende Diagnostik: ID374.02, 245 Gene
AAAS,
AARS1,
ABCA1,
ABCD1,
ABHD12,
ACOX1,
ADA2,
ADCY6,
ADGRG6,
ADPRS,
AGTPBP1,
AGXT,
AIFM1,
AMACR,
AP1S1,
AP5Z1,
APOA1,
APTX,
AR,
ARHGEF10,
ARL6IP1,
ARSA,
ASAH1,
ASCC1,
ATAD3A,
ATL1,
ATL3,
ATM,
ATP1A1,
ATP7A,
ATP13A2,
ATXN1,
ATXN2,
ATXN3,
ATXN7,
ATXN10,
B4GALNT1,
BAG3,
BCKDHB,
BICD2,
BSCL2,
CADM3,
CAPN1,
CD59,
CFAP276,
CHCHD10,
CLP1,
CNTNAP1,
COA7,
COQ7,
COX6A1,
COX20,
CPOX,
CTDP1,
CYP2U1,
CYP27A1,
DARS2,
DCTN1,
DHH,
DHTKD1,
DHX9,
DMXL2,
DNAJB2,
DNAJC3,
DNM2,
DNMT1,
DRP2,
DST,
DYNC1H1,
EGR2,
ELP1,
EMILIN1,
ERCC6,
ERCC8,
ETFDH,
EXOSC3,
FA2H,
FAH,
FBLN5,
FBXO38,
FDXR,
FGD4,
FICD,
FIG4,
FLVCR1,
FMR1,
FXN,
GALC,
GAN,
GARS1,
GBA2,
GBF1,
GDAP1,
GJB1,
GLA,
GNB4,
GSN,
HADHA,
HADHB,
HARS1,
HEXA,
HEXB,
HINT1,
HK1,
HMBS,
HPDL,
HSPB1,
HSPB3,
HSPB8,
HYCC1,
IARS2,
IGHMBP2,
INF2,
ITPR3,
JAG1,
JPH1,
KARS1,
KIF1A,
KIF1B,
KIF5A,
LITAF,
LMNA,
LRSAM1,
LYST,
MAG,
MARS1,
MCM3AP,
MED25,
MFN2,
MMACHC,
MME,
MORC2,
MPV17,
MPZ,
MT-ATP6,
MTMR2,
MTRFR,
MTTP,
MYH14,
NAGA,
NAGLU,
NARS1,
NDC1,
NDRG1,
NDUFS6,
NEFH,
NEFL,
NEMF,
NFASC,
NGF,
NTRK1,
NUDT2,
OPA1,
OPA3,
PDHA1,
PDK3,
PDXK,
PDYN,
PEX7,
PEX10,
PHYH,
PIEZO2,
PIGB,
PLA2G6,
PLAAT3,
PLEKHG5,
PLP1,
PMM2,
PMP2,
PMP22,
PNKP,
PNPLA6,
PNPT1,
POLG,
POLR3A,
POLR3B,
PPOX,
PRDM12,
PRNP,
PRPS1,
PRX,
PTRH2,
RAB7A,
REEP1,
RETREG1,
RTN2,
SACS,
SAMD9L,
SARS1,
SBF1,
SBF2,
SCARB2,
SCN9A,
SCN10A,
SCN11A,
SCO2,
SEPTIN9,
SETX,
SH3TC2,
SIGMAR1,
SLC5A6,
SLC5A7,
SLC12A6,
SLC25A19,
SLC25A46,
SLC52A2,
SLC52A3,
SMN1,
SMN2,
SORD,
SOX10,
SPAST,
SPG7,
SPG11,
SPTAN1,
SPTBN4,
SPTLC1,
SPTLC2,
SURF1,
SYT2,
TBCE,
TECPR2,
TFG,
TRIM2,
TRIP4,
TRMT5,
TRPV4,
TTPA,
TTR,
TUBB3,
TWNK,
TYMP,
UBA1,
UCHL1,
VAPB,
VCP,
VPS13D,
VRK1,
VWA1,
WARS1,
WNK1,
XK,
XPA,
YARS1,
ZFYVE26
Inkludierte Phänotypen
Hereditäre motorisch-sensible Neuropathie (HMSN): 64 Gene
AARS1,
AIFM1,
ARHGEF10,
ATP1A1,
CADM3,
CNTNAP1,
COX6A1,
DHTKD1,
DNM2,
DYNC1H1,
EGR2,
FBLN5,
FGD4,
FIG4,
GAN,
GBF1,
GDAP1,
GJB1,
GNB4,
HARS1,
HINT1,
HK1,
INF2,
ITPR3,
JAG1,
JPH1,
KARS1,
KIF1B,
LITAF,
LMNA,
LRSAM1,
MARS1,
MED25,
MFN2,
MME,
MORC2,
MPV17,
MPZ,
MTMR2,
NAGLU,
NDRG1,
NEFH,
NEFL,
PDK3,
PDXK,
PLEKHG5,
PMP2,
PMP22,
PNKP,
POLR3B,
PRPS1,
PRX,
RAB7A,
SBF1,
SBF2,
SH3TC2,
SLC12A6,
SLC25A46,
SPG11,
SPTLC1,
SURF1,
TRIM2,
VCP,
YARS1
Hereditäre sensorische und autonome Neuropathie (HSAN, HSN): 16 Gene
ATL1,
ATL3,
DNMT1,
DST,
ELP1,
KIF1A,
NGF,
NTRK1,
PRDM12,
RETREG1,
SCN9A,
SCN11A,
SPTLC1,
SPTLC2,
TECPR2,
WNK1
Spinale Muskelatrophie (SMA, HMN): 39 Gene
AR,
ASAH1,
ASCC1,
ATP7A,
BAG3,
BICD2,
BSCL2,
CHCHD10,
COQ7,
DCTN1,
DNAJB2,
DYNC1H1,
EMILIN1,
EXOSC3,
FBXO38,
GARS1,
HSPB1,
HSPB3,
HSPB8,
IGHMBP2,
PLEKHG5,
REEP1,
RTN2,
SETX,
SIGMAR1,
SLC5A7,
SLC25A46,
SMN1,
SMN2,
SORD,
SPTAN1,
SYT2,
TRIP4,
TRPV4,
UBA1,
VAPB,
VRK1,
VWA1,
WARS1