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Multigen-Diagnostik

Primäre Immundefekte, umfassende Diagnostik

Panel-Nummer: ID380.01

Gene (435)

GenotypOMIM
Genotyp
ErbgangOMIM
Phänotyp
Phänotyp
ADAR AGR2 AICDA AIRE AK2
ALPI ALPK1 ANGPT1 ANKZF1 AP1S3
AP3B1 AP3D1 ARHGEF1 ARPC1B ARPC5
ATAD3A ATM ATP6AP1 B2M BACH2
BCL10 BCL11B BLM BLNK BLOC1S6
BTK C1QA C1QB C1QC C1R
C1S C2 C2ORF69 C3 C5
C6 C7 C8A C8B C9
CARD10 CARD11 CARD14 CARD8 CARD9
CARMIL2 CASP10 CASP8 CBLB CCBE1
CD19 CD247 CD27 CD28 CD3D
CD3E CD3G CD4 CD40 CD40LG
CD46 CD55 CD59 CD70 CD79A
CD79B CD81 CD8A CDC42 CDCA7
CEBPE CFB CFD CFH CFHR1
CFI CFP CFTR CHD7 CIB1
CIITA CLPB COL7A1 COPA CORO1A
CR2 CSF2RA CSF2RB CSF3R CTC1
CTLA4 CTNNBL1 CTPS1 CTSC CXCR2
CXCR4 CYBA CYBB CYBC1 DBR1
DCLRE1B DCLRE1C DEF6 DIAPH1 DKC1
DNAJC21 DNASE1L3 DNASE2 DNMT3B DOCK11
DOCK2 DOCK8 DPP9 DUT EFL1
ELANE ELF4 EPG5 ERBIN ERCC6L2
EXTL3 F12 FADD FAS FASLG
FAT4 FCGR3A FCHO1 FCN3 FERMT1
FERMT3 FGL2 FLT3LG FMNL2 FNIP1
FOXI3 FOXN1 FOXP3 FPR1 G6PC3
G6PD GATA1 GATA2 GFI1 GIMAP5
GINS1 GUCY2C HAVCR2 HAX1 HELLS
HMOX1 HPS1 HPS4 HPS6 HSPA1L
HTRA2 HYOU1 ICOS ICOSLG IFIH1
IFNAR1 IFNAR2 IFNG IFNGR1 IFNGR2
IGLL1 IKBKB IKZF1 IKZF2 IKZF3
IL10 IL10RA IL10RB IL12B IL12RB1
IL17F IL17RA IL17RC IL1R1 IL1RN
IL21 IL21R IL23R IL2RA IL2RB
IL2RG IL36RN IL6R IL6ST IL7R
INO80 IPO8 IRAK4 IRF1 IRF2BP2
IRF3 IRF4 IRF7 IRF8 IRF9
ISG15 ITCH ITGB2 ITK ITPKB
IVNS1ABP JAGN1 JAK1 JAK3 KCNA5
KDM6A KMT2A KMT2D KRAS LACC1
LAMTOR2 LAT LCK LCP2 LIG1
LIG4 LPIN2 LRBA LRRC8A LYN
LYST MAGT1 MALT1 MAP3K14 MBL2
MCM10 MCM4 MCTS1 MECOM MEFV
MOGS MPEG1 MPO MRTFA MS4A1
MSN MTHFD1 MVK MYD88 MYO5B
MYSM1 NBN NCF1 NCF2 NCF4
NCKAP1L NCSTN NFAT5 NFE2L2 NFKB1
NFKB2 NFKBIA NHEJ1 NHP2 NLRC4
NLRP1 NLRP12 NLRP3 NOD2 NOP10
NPC1 NRAS NSMCE3 NUDCD3 OAS1
ORAI1 OTULIN PARN PAX1 PEPD
PGM3 PI4KA PIK3CD PIK3CG PIK3R1
PLCG2 PLG PNP POLA1 POLD1
POLD3 POLE POLR3A POLR3C POLR3F
POMP PRF1 PRIM1 PRKCD PRKDC
PSENEN PSMA3 PSMB10 PSMB4 PSMB8
PSMB9 PSTPIP1 PTCRA PTEN PTPN2
PTPRC RAB27A RAC2 RAG1 RAG2
RANBP2 RASGRP1 RBCK1 RC3H1 RECQL4
REL RELA RELB RFX5 RFXANK
RFXAP RHBDF2 RHOH RIPK1 RNASEH2A
RNASEH2B RNASEH2C RNF168 RNF31 RORC
RPSA RTEL1 SAMD9 SAMD9L SAMHD1
SASH3 SBDS SCGN SEC61A1 SERPING1
SGPL1 SH2D1A SH3KBP1 SKIC2 SKIC3
SLC19A1 SLC29A3 SLC35C1 SLC37A4 SLC39A7
SLC46A1 SLC7A7 SLC9A3 SLCO2A1 SMARCAL1
SMARCD2 SOCS1 SP110 SPI1 SPINK5
SPPL2A SRP54 STAT1 STAT2 STAT3
STAT4 STAT5B STAT6 STIM1 STING1
STK4 STX11 STXBP2 STXBP3 SYK
TAP1 TAP2 TAPBP TAFAZZIN TBK1
TBX1 TBX21 TCF3 TCN2 TERC
TERT TET2 TFRC TGFB1 TGFBR1
TGFBR2 TICAM1 TINF2 TLR3 TLR7
TLR8 TMC6 TMC8 TNFAIP3 TNFRSF11A
TNFRSF13B TNFRSF13C TNFRSF1A TNFRSF4 TNFRSF9
TOM1 TOP2B TPP2 TRAF3IP2 TREX1
TRIM22 TRNT1 TTC7A TYK2 UNC119
UNC13D UNC93B1 UNG USB1 USP18
VPS13B VPS45 WAS WDR1 WIPF1
XIAP ZAP70 ZBTB24 ZNF341 ZNFX1

Akkreditiertes Verfahren: ja

Methodik

Mittels Next-Generation-Sequencing (NGS) werden die o. g. Gene parallel analysiert (DNA-Sequenz, ggf. Kopienzahlvariation (CNV)).

Als Bestätigungsanalyse kann ggf. eine Sanger-Sequenzanalyse bzw. eine MLPA-Analyse (Multiplex-Ligation-dependent-Product-Amplification) durchgeführt werden.

Diagnostik

Gen-Panel: ID380.01, 435 Gene (930,7 kb) 

ACD, ACP5, ADA, ADA2, ADAM17, ADAR, AGR2, AICDA, AIRE, AK2, ALPI, ALPK1, ANGPT1, ANKZF1, AP1S3, AP3B1, AP3D1, ARHGEF1, ARPC1B, ARPC5, ATAD3A, ATM, ATP6AP1, B2M, BACH2, BCL10, BCL11B, BLM, BLNK, BLOC1S6, BTK, C1QA, C1QB, C1QC, C1R, C1S, C2, C2ORF69, C3, C5, C6, C7, C8A, C8B, C9, CARD10, CARD11, CARD14, CARD8, CARD9, CARMIL2, CASP10, CASP8, CBLB, CCBE1, CD19, CD247, CD27, CD28, CD3D, CD3E, CD3G, CD4, CD40, CD40LG, CD46, CD55, CD59, CD70, CD79A, CD79B, CD81, CD8A, CDC42, CDCA7, CEBPE, CFB, CFD, CFH, CFHR1, CFI, CFP, CFTR, CHD7, CIB1, CIITA, CLPB, COL7A1, COPA, CORO1A, CR2, CSF2RA, CSF2RB, CSF3R, CTC1, CTLA4, CTNNBL1, CTPS1, CTSC, CXCR2, CXCR4, CYBA, CYBB, CYBC1, DBR1, DCLRE1B, DCLRE1C, DEF6, DIAPH1, DKC1, DNAJC21, DNASE1L3, DNASE2, DNMT3B, DOCK11, DOCK2, DOCK8, DPP9, DUT, EFL1, ELANE, ELF4, EPG5, ERBIN, ERCC6L2, EXTL3, F12, FADD, FAS, FASLG, FAT4, FCGR3A, FCHO1, FCN3, FERMT1, FERMT3, FGL2, FLT3LG, FMNL2, FNIP1, FOXI3, FOXN1, FOXP3, FPR1, G6PC3, G6PD, GATA1, GATA2, GFI1, GIMAP5, GINS1, GUCY2C, HAVCR2, HAX1, HELLS, HMOX1, HPS1, HPS4, HPS6, HSPA1L, HTRA2, HYOU1, ICOS, ICOSLG, IFIH1, IFNAR1, IFNAR2, IFNG, IFNGR1, IFNGR2, IGLL1, IKBKB, IKZF1, IKZF2, IKZF3, IL10, IL10RA, IL10RB, IL12B, IL12RB1, IL17F, IL17RA, IL17RC, IL1R1, IL1RN, IL21, IL21R, IL23R, IL2RA, IL2RB, IL2RG, IL36RN, IL6R, IL6ST, IL7R, INO80, IPO8, IRAK4, IRF1, IRF2BP2, IRF3, IRF4, IRF7, IRF8, IRF9, ISG15, ITCH, ITGB2, ITK, ITPKB, IVNS1ABP, JAGN1, JAK1, JAK3, KCNA5, KDM6A, KMT2A, KMT2D, KRAS, LACC1, LAMTOR2, LAT, LCK, LCP2, LIG1, LIG4, LPIN2, LRBA, LRRC8A, LYN, LYST, MAGT1, MALT1, MAP3K14, MBL2, MCM10, MCM4, MCTS1, MECOM, MEFV, MOGS, MPEG1, MPO, MRTFA, MS4A1, MSN, MTHFD1, MVK, MYD88, MYO5B, MYSM1, NBN, NCF1, NCF2, NCF4, NCKAP1L, NCSTN, NFAT5, NFE2L2, NFKB1, NFKB2, NFKBIA, NHEJ1, NHP2, NLRC4, NLRP1, NLRP12, NLRP3, NOD2, NOP10, NPC1, NRAS, NSMCE3, NUDCD3, OAS1, ORAI1, OTULIN, PARN, PAX1, PEPD, PGM3, PI4KA, PIK3CD, PIK3CG, PIK3R1, PLCG2, PLG, PNP, POLA1, POLD1, POLD3, POLE, POLR3A, POLR3C, POLR3F, POMP, PRF1, PRIM1, PRKCD, PRKDC, PSENEN, PSMA3, PSMB10, PSMB4, PSMB8, PSMB9, PSTPIP1, PTCRA, PTEN, PTPN2, PTPRC, RAB27A, RAC2, RAG1, RAG2, RANBP2, RASGRP1, RBCK1, RC3H1, RECQL4, REL, RELA, RELB, RFX5, RFXANK, RFXAP, RHBDF2, RHOH, RIPK1, RNASEH2A, RNASEH2B, RNASEH2C, RNF168, RNF31, RORC, RPSA, RTEL1, SAMD9, SAMD9L, SAMHD1, SASH3, SBDS, SCGN, SEC61A1, SERPING1, SGPL1, SH2D1A, SH3KBP1, SKIC2, SKIC3, SLC19A1, SLC29A3, SLC35C1, SLC37A4, SLC39A7, SLC46A1, SLC7A7, SLC9A3, SLCO2A1, SMARCAL1, SMARCD2, SOCS1, SP110, SPI1, SPINK5, SPPL2A, SRP54, STAT1, STAT2, STAT3, STAT4, STAT5B, STAT6, STIM1, STING1, STK4, STX11, STXBP2, STXBP3, SYK, TAP1, TAP2, TAPBP, TAFAZZIN, TBK1, TBX1, TBX21, TCF3, TCN2, TERC, TERT, TET2, TFRC, TGFB1, TGFBR1, TGFBR2, TICAM1, TINF2, TLR3, TLR7, TLR8, TMC6, TMC8, TNFAIP3, TNFRSF11A, TNFRSF13B, TNFRSF13C, TNFRSF1A, TNFRSF4, TNFRSF9, TOM1, TOP2B, TPP2, TRAF3IP2, TREX1, TRIM22, TRNT1, TTC7A, TYK2, UNC119, UNC13D, UNC93B1, UNG, USB1, USP18, VPS13B, VPS45, WAS, WDR1, WIPF1, XIAP, ZAP70, ZBTB24, ZNF341, ZNFX1

* auch als Einzelgen-Diagnostik mittels Sanger-Sequenzierung verfügbar
** auch als Einzelgen-Diagnostik mittels MLPA-Analyse verfügbar

Material

3 - 5 ml EDTA-Blut

Dauer

4 - 6 Wochen

Kosten

Die Kosten werden bei bestehender medizinischer Indikation über einen Überweisungsschein Typ 10 (EBM) abgerechnet. Humangenetische Leistungen sind nicht budgetrelevant.

Für privatversicherte Patienten sowie private Kostenträger (Krankenhäuser etc.) können auf Wunsch entsprechende Kostenvoranschläge erstellt werden.  


Stand: 29.07.2025